NZ765592A

NZ765592A - Methods and compositions for targeted genetic modifications and methods of use

Info

Publication number: NZ765592A
Application number: NZ765592A
Authority: NZ
Inventors: Junko Kuno; David M Valenzuela; David Frendewey; Wojtek Auerbach; Gustavo Droguett; Anthony Gagliardi
Original assignee: Regeneron Pharma
Priority date: 2014-06-26
Filing date: 2015-06-26
Publication date: 2021-02-26

Abstract

Methods and compositions are provided for generating targeted genetic modifications on the Y chromosome or a challenging target locus. Compositions include an in vitro culture comprising an XY pluripotent and/or totipotent animal cell (i.e., XY ES cells or XY iPS cells) having a modification that decreases the level and/or activity of an Sry protein; and, culturing these cells in a medium that promotes development of XY F0 fertile females. Such compositions find use in various methods for making a fertile female XY non-human mammal in an F0 generation.

Description

METHODS AND COMPOSITIONS FOR TARGETED GENETIC MODIFICATIONS AND METHODS OF USE This application is a onal application from New Zealand Patent Application Number 728561, the entire disclosures of which are incorporated herein by reference.

CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. ,582, filed June 26, 2014, and of U.S. Provisional Application No. 62/017,627, filed June 26, 2014, each of which is hereby incorporated herein in its entirety by reference.

REFERENCE TO A CE LISTING SUBMITTED AS A TEXT FILE VIA EFS WEB The official copy of the sequence listing is submitted electronically via EFS-Web as an ASCII formatted ce listing with a file named 463545SEQLIST.TXT, created on June 25, 2015, and having a size of 14 kilobytes, and is filed concurrently with the ication. The sequence listing contained in this ASCII formatted nt is part of the ication and is herein incorporated by reference in its entirety.

FIELD The invention relates to the methods and compositions for maintaining or ing pluripotent and/or totipotent cells and methods and compositions for generating cell populations and transgenic animals.

BACKGROUND Perhaps due to unique structural features of the Y chromosome, conventional gene targeting strategies in mouse embryonic stem cells to generate mutations on the Y-linked genes have had limited success. Therefore, often the understanding of the ons of murine Y-linked genes is limited to ts gained from studies of mice that carry spontaneous deletions, random gene traps insertions or autosomal transgenes. Methods are needed to improve the ability to target a genomic locus on the Y chromosome.

The Sry protein (sex-determining region Y) is the key regulator of male sex ination in placental mammals. The Sry gene, also known as the Testis Determining Factor (TDF), resides on the Y chromosome. Sry is thought to be a transcription factor that binds DNA through its High Mobility Group (HMG) domain. Expression of the mouse Sry gene is restricted to the genital ridge in a narrow time window around day 11 of embryonic development; both Sry mRNA and n are ed. Sufficient Sry must be made within this time window to convert the ntial genital ridge toward the male testis forming program while inhibiting the female program of ovary development. In adult testes a circular Sry transcript is detected but not the Sry protein. Mutations in the Sry gene that cause the production of an inactive Sry protein or that alter the timing and th of gene expression can cause male to female sex reversal, resulting in animals that have an X and a Y chromosome but are anatomically female. So-called XY females are often sterile or have a low fertility. Being able to control sex determination by regulation of the Sry would have great value in the production of cally modified animals.

SUMMARY A method for making an XY embryonic stem (ES) cell line capable of producing a fertile XY female non-human mammal in an F0 generation is provided. The method comprises: (a) modifying a non-human mammalian XY embryonic stem (ES) cell to have a modification that decreases the level and/or activity of an Sry protein; and, (b) culturing the ed ES cell line under conditions that allow for making an ES cell line e of producing a fertile XY female non-human mammal in an F0 generation.

A method for making a fertile XY female non-human mammal in an F0 generation is also provided. The method comprises: (a) ucing the man mammalian XY ES cell made by the above method having a modification that decreases the level and/or activity of an Sry protein into a host embryo; (b) gestating the host embryo; and, (c) ing an F0 XY female non-human mammal, wherein upon attaining sexual maturity the F0 XY female non-human mammal is fertile. In one embodiment, the female XY F0 non- human mammal is fertile when crossed to a wild type mouse. In specific embodiments, the wild type mouse is C57BL/6.

In one ment, the non-human mammalian XY ES cell is from a rodent. In a specific embodiment, the rodent is a mouse. In one embodiment, the mouse XY ES cell is derived from a 129 strain. In one embodiment, the mouse XY ES cell is a VGFl mouse ES cell. In one embodiment, the mouse XY ES cell comprises a Y chromosome derived from the 129 strain. In one embodiment, the mouse XY ES cell is from a C57BL/6 strain. In another embodiment the rodent is a rat or a hamster.

In some embodiments, the decreased level and/or activity of the Sry protein results from a genetic modification in the Sry gene. In some such methods, the genetic WO 00805 modification in the Sry gene comprises an insertion of one or more nucleotides, a deletion of one or more nucleotides, a tution of one or more nucleotides, a knockout, a knockin, a replacement of an endogenous c acid ce with a homologous, heterologous, or orthologous nucleic acid sequence, or a combination thereof.

In the methods provided herein, the targeted genetic modification can comprises an insertion, a deletion, a knockout, a n, a point mutation, or a combination thereof. In another ment, the targeted genetic modification is on an autosome.

In some embodiments, the modification of the Sry gene comprises an insertion of a selectable marker and/or a reporter gene operably linked to a promoter active in the non- human mammalian ES cell. In some embodiments, the the modification of the Sry gene comprises an insertion of a reporter gene operably linked to the nous Sry promoter. In a specific embodiment, the reporter gene encodes the reporter protein LacZ.

In one embodiment, the culturing step comprises ing the non-human mammalian XY ES cell in a medium comprising a base medium and supplements suitable for maintaining the non-human mammalian ES cell in culture, n the medium is a low- osmolality medium. In one embodiment, the low-osmolality medium exhibits an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg. In other embodiments the low- osmolality medium exhibits one or more of the following characteristic: a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50 mM to about 110 mM; a carbonic acid salt concentration of about l7mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt concentration of about 85mM to about 130 mM; and/or a combination of any two or more thereof.

In some ments, upon introduction of the non-human mammalian XY ES cells into a host embryo and following gestation of the host embryo, at least 80% at least 85%, at least 90%, or at least 95% of the F0 non-human mammals are XY females which upon attaining sexual maturity the F0 XY female non-human mammal is fertile.

In one embodiment, the man mammalian XY ES cell comprises a target genomic locus on the Y chromosome comprising a recognition site for a se agent, and wherein the nuclease agent induces a nick or double-strand break at the recognition site. Such a method can r comprise exposing the ES cell to the nuclease agent in the ce of a targeting vector comprising an insert polynucleotide, wherein following exposure to the nuclease agent and the targeting vector, the ES cell is modified to contain the insert polynucleotide. In one embodiment, the nuclease agent is an mRNA encoding a nuclease. In specific embodiments, the se agent is (a) a zinc finger nuclease (ZEN); (b) is a 2015/038001 Transcription Activator-Like Effector se (TALEN); or (C) a meganuclease. In other embodiments, the nuclease agent comprises a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated (Cas) protein and a guide RNA (gRNA). In such methods, the guide RNA (gRNA) ses (a) a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) RNA (chNA) that targets the first recognition site; and (b) a trans-activating CRISPR RNA (trachNA). In some cases, the recognition site is immediately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence. In one embodiment, the Cas protein is Cas9.

Also provided is an in vitro culture comprising the non-human mammalian XY ES cell line according to any of the methods provided herein.

An in vitro culture is provided and comprises (a) a non-human mammalian XY embryonic stem (ES) cell having a modification that decreases the level and/or activity of an Sry n; and, (b) a medium comprising a base medium and supplements suitable for maintaining the non-human mammalian ES cell in culture. In one embodiment, the base medium ts an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg. In other embodiments, the base medium ts one or more of the following characteristic: a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50 mM to about 110 mM; a carbonic acid salt concentration of about l7mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt concentration of about 85mM to about 130 mM; and/or a ation of any two or more thereof. In one embodiment, the non-human mammalian XY ES cell is from a rodent. In one embodiment, the rodent is a mouse or a rat. In one embodiment, the mouse XY ES cell is a VGFl mouse ES cell. In one embodiment, the rodent is a rat or a hamster. In one embodiment, the decreased level and/or activity of the Sry protein is from a genetic cation in the Sry gene. In one embodiment, the c modification in the Sry gene comprises an insertion of one or more tides, a on of one or more nucleotides, a substitution of one or more nucleotides, a knockout, a knockin, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence or a ation thereof. In one embodiment, the non-human mammalian ES cell comprises one, two, three or more targeted genetic modifications. In one embodiment, the targeted genetic modification comprises an insertion, a deletion, a knockout, a knockin, a point on, or a combination thereof. In one embodiment, the targeted genetic modification comprises at least one ion of a heterologous polynucleotide into the genome of the XY ES cell. In one ment, the targeted genetic modification is on an autosome. In one embodiment, the base medium exhibits 50 i 5 mM NaCl, 26 i 5 mM carbonate, and 218 i 22 mOsm/kg. In one embodiment, the base medium ts about 3 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 218 g. In one embodiment, the base medium exhibits 87 i 5 mM NaCl, 18 i 5 mM carbonate, and 261 i 26 mOsm/kg. In one embodiment, the base medium exhibits about 5.1 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 261 mOsm/kg. In one embodiment, the base medium ts 110 i 5 mM NaCl, 18 i 5 mM carbonate, and 294 i 29 mOsm/kg. In one embodiment, the base medium exhibits about 6.4 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 294 mOsm/kg. In one embodiment, the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, and 270 i 27 mOsm/kg. In one embodiment, the base medium ts about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 270 mOsm/kg. In one embodiment, the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, 86 i 5 mM e, and 322 i 32 mOsm/kg. In one embodiment, the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, 15.5 mg/mL glucose, and 322 mOsm/kg. In one ment, upon introduction of the non-human mammalian XY ES cells into a host embryo and following gestation of the host embryo, at least 80% of the F0 non-human mammals are XY females which upon ing sexual maturity the F0 XY female non-human mammal is fertile.

Further provided is a method for making a fertile female XY non-human mammal in an F0 generation, comprising: (a) culturing a donor non-human mammalian XY embryonic stem (ES) cell having a modification that decreases the level and/or activity of an Sry protein in a medium comprising a base medium and supplements suitable for maintaining the non-human mammalian ES cell in culture, (b) introducing the donor XY non-human ian ES cell into a host ; (c) gestating the host embryo; and, (d) obtaining an F0 XY female non-human mammal, wherein upon attaining sexual maturity the F0 XY female non-human mammal is fertile. In one embodiment, the medium exhibits an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg. In other embodiments, the medium exhibits a characteristic comprising one or more of the following: a tivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a tration of about 50mM to about 110 mM; a carbonic acid salt concentration of about 17 mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt concentration of about 85 mM to about 130 mM; and/or a ation of any two or more thereof; In one embodiment, the non-human mammalian XY ES cell is from a rodent. In one embodiment, the rodent is a mouse or a rat. In one embodiment, the mouse XY ES cell is a VGFl mouse ES cell. In one embodiment, the rodent is a rat or a hamster. In one embodiment, the decreased level and/or activity of the Sry protein is from a genetic modification in the Sry gene. In one embodiment, the genetic modification in the Sry gene comprises an ion of one or more nucleotides, a deletion of one or more nucleotides, a tution of one or more nucleotides, a knockout, a knockin, a replacement of an endogenous nucleic acid sequence with a heterologous c acid sequence or a combination f. In one embodiment, the non-human mammalian ES cell comprises one, two, three or more targeted genetic modifications. In one embodiment, the targeted c modification comprises an insertion, a deletion, a knockout, a knockin, a point on, or a combination thereof. In one embodiment, the targeted genetic modification comprises at least one insertion of a heterologous polynucleotide into a genome of the XY ES cell. In one embodiment, the targeted genetic modification is on an autosome. In one embodiment, the base medium exhibits 50 i 5 mM NaCl, 26 i 5 mM carbonate, and 218 i 22 g. In one embodiment, the base medium exhibits about 3 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 218 mOsm/kg. In one embodiment, the base medium exhibits 87 i 5 mM NaCl, 18 i 5 mM carbonate, and 261 i 26 mOsm/kg. In one embodiment, the base medium exhibits about 5.1 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 261 mOsm/kg. In one embodiment, the base medium exhibits 110 i 5 mM NaCl, 18 i 5 mM carbonate, and 294 i 29 mOsm/kg. In one embodiment, the base medium ts about 6.4 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 294 mOsm/kg. In one embodiment, the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, and 270 i 27 mOsm/kg. In one embodiment, the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 270 mOsm/kg. In one ment, wherein the base medium exhibits 87 i mM NaCl, 26 i 5 mM carbonate, 86 i 5 mM glucose, and 322 i 32 mOsm/kg. In one embodiment, n the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, 15.5 mg/mL glucose, and 322 mOsm/kg.

Further provided are methods of producing a enic non-human mammal homozygous for a targeted genetic mutation in the F1 generation comprising: (a) crossing an F0 XY fertile female having a decreased level and/or activity of the Sry protein with a cohort clonal sibling, derived from the same ES cell clone, F0 XY male non-human mammal, wherein the F0 XY fertile female non-human mammal and the F0 XY male non-human mammal each is heterozygous for the genetic mutation; and,(b) obtaining an F1 progeny mouse that is homozygous for the c modification.

A method for modifying a target genomic locus on the Y chromosome in a cell is also ed and comprises (a) providing a cell comprising a target genomic locus on the Y some comprising a recognition site for a nuclease agent, (b) introducing into the cell (i) the nuclease agent, wherein the nuclease agent induces a nick or double-strand break at the first recognition site; and, (ii) a first targeting vector comprising a first insert polynucleotide ﬂanked by a first and a second homology arm corresponding to a first and a second target site located in sufficient proximity to the first recognition site; and, (c) identifying at least one cell comprising in its genome the first insert polynucleotide ated at the target genomic locus. In one ment, a sum total of the first homology arm and the second homology arm is at least 4kb but less than 150kb. In one ment, the length of the first homology arm and/or the second homology arm is at least 400 bp but less than 1000 bp. In another embodiment, the length of the first homology arm and/or the second homology arm is from about 700 bp to about 800 bp.

Further provided is a method for modifying a target genomic locus on the Y chromosome in a cell is provided and ses: (a) providing a cell comprising a target genomic locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) introducing into the cell a first targeting vector comprising a first insert polynucleotide flanked by a first and a second gy arm corresponding to a first and a second target site; and, (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus. In one embodiment, the length of the first gy arm and/or the second homology arm is at least 400 bp but less than 1000 bp.

In another embodiment, the length of the first homology arm and/or the second homology arm is from about 700 bp to about 800 bp. In one embodiment, the cell is a mammalian cell.

In one embodiment, the ian cell is a non-human cell. In one embodiment, the mammalian cell is from a rodent. In one embodiment, the rodent is a rat, a mouse or a hamster. In one embodiment, the cell is a pluripotent cell. In one embodiment, the mammalian cell is an induced pluripotent stem (iPS) cell. In one embodiment, the pluripotent cell is a non-human embryonic stem (ES) cell. In one embodiment, the pluripotent cell is a rodent embryonic stem (ES) cell, a mouse nic stem (ES) cell or a rat embryonic stem (ES) cell. In one embodiment, the nuclease agent is an mRNA encoding a nuclease. In one embodiment, the nuclease agent is a zinc finger se (ZFN). In one embodiment, the nuclease agent is a Transcription Activator-Like Effector se (TALEN). In one embodiment, the se agent is a meganuclease. In some embodiments, the nuclease agent comprises a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)- associated (Cas) protein and a guide RNA (gRNA). In such a method the guide RNA (gRNA) can comprise (a) a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) WO 00805 RNA (chNA) that targets the first recognition site; and (b) a trans-activating CRISPR RNA (trachNA). In one embodiment, the first or the second recognition sites are immediately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence. In some embodiments, the Cas protein is Cas9.

In some embodiments, the cation comprises a deletion of an nous nucleic acid sequence. In some embodiments, the deletion ranges from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, or from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb. In a specific embodiment, the deletion is at least 500 kb. In one embodiment, the cell is a mammalian cell.

In one embodiment, the mammalian cell is a non-human cell. In one embodiment, the ian cell is from a rodent. In one embodiment, the rodent is a rat, a mouse or a hamster. In one embodiment, the cell is a pluripotent cell. In one embodiment, the mammalian cell is an induced pluripotent stem (iPS) cell. In one embodiment, the otent cell is a non-human embryonic stem (ES) cell. In one ment, the pluripotent cell is a rodent embryonic stem (ES) cell, a mouse embryonic stem (ES) cell or a rat embryonic stem (ES) cell. In some embodiments, the nuclease agent comprises a Clustered Regularly Interspaced Short Palindromic s (CRISPR)-associated (Cas) protein and a guide RNA (gRNA). In such a method the guide RNA (gRNA) can comprise (a) a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) RNA (chNA) that s the first recognition site; and (b) a trans-activating CRISPR RNA (trachNA). In one embodiment, the first or the second recognition sites are immediately ﬂanked by a Protospacer Adjacent Motif (PAM) ce. In some embodiments, the Cas protein is Cas9. In one embodiment, the nuclease agent is a zinc finger se (ZFN). In one embodiment, the nuclease agent is a Transcription Activator-Like Effector Nuclease (TALEN). In one embodiment, the nuclease agent is a meganuclease.

Methods for modifying the Y chromosome comprising exposing the Y chromosome to a Cas protein and a CRISPR RNA in the presence of a large targeting vector (LTVEC) comprising a nucleic acid sequence of at least 10 kb and comprises following exposure to the Cas protein, the CRISPR RNA, and the LTVEC, the Y chromosome is modified to contain at least 10 kb nucleic acid sequence. The LTVEC can comprise a nucleic 2015/038001 acid sequence of at least 20 kb, at least 30 kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, or at least 90 kb. In other embodiments, the LTVEC comprises a nucleic acid sequence of at least 100 kb, at least 150 kb, or at least 200 kb.

Further ed is a method for modifying a target genomic locus on the Y chromosome, comprising: (a) ing a mammalian cell comprising the target genomic locus on the Y chromosome, wherein the target genomic locus comprises a guide RNA (gRNA) target sequence; (b) introducing into the ian cell: (i) a large targeting vector (LTVEC) comprising a first nucleic acid ﬂanked with targeting arms homologous to the target genomic locus, wherein the LTVEC is at least 10 kb; (ii) a first expression construct comprising a first promoter operably linked to a second nucleic acid ng a Cas n, and (iii) a second expression construct comprising a second promoter operably linked to a third nucleic acid encoding a guide RNA (gRNA) sing a nucleotide sequence that hybridizes to the gRNA target sequence and a trans-activating CRISPR RNA (trachNA), wherein the first and the second promoters are active in the ian cell; and (c) identifying a modified mammalian cell comprising a targeted genetic cation at the target genomic locus on the Y chromosome. In other embodiments, the LTVEC is at least 15 kb, at least 20 kb, at least 30kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, or at least 90 kb. In other embodiments, the LTVEC is at least 100 kb, at least 150 kb, or at least 200 kb. In one embodiment, the mammalian cell is a non-human mammalian cell. In one embodiment, the mammalian cell is a fibroblast cell. In one embodiment, the mammalian cell is from a rodent. In one embodiment, the rodent is a rat, a mouse, or a hamster. In one embodiment, the mammalian cell is a pluripotent cell. In one embodiment, the pluripotent cell is an induced pluripotent stem (iPS) cell. In one embodiment, the otent cell is a mouse embryonic stem (ES) cell or a rat embryonic stem (ES) cell. In one embodiment, the pluripotent cell is a developmentally restricted human progenitor cell. In one embodiment, the Cas protein is a Cas9 protein. In one embodiment, the gRNA target sequence is ately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence. In one embodiment, the sum total of 5’ and 3’ homology arms of the LTVEC is from about 10 kb to about 150 kb. In one embodiment, the sum total of the 5’ and the 3’ homology arms of the LTVEC is from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 120 kb, or from about 120 kb to 150 kb.

In one embodiment, the targeted genetic modification comprises: (a) a replacement of an endogenous nucleic acid sequence with a homologous or an orthologous nucleic acid sequence; (b) a deletion of an endogenous nucleic acid sequence; (c) a deletion of an endogenous nucleic acid sequence, wherein the deletion ranges from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, or from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb; (d) insertion of an exogenous nucleic acid sequence; (e) insertion of an ous c acid ce ranging from about 5kb to about 10kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, from about 150 kb to about 200 kb, from about 200 kb to about 250 kb, from about 250 kb to about 300 kb, from about 300 kb to about 350 kb, or from about 350 kb to about 400 kb; (f) insertion of an exogenous nucleic acid sequence comprising a homologous or an ogous nucleic acid ce; (g) insertion of a chimeric nucleic acid sequence comprising a human and a non-human nucleic acid sequence; (h) ion of a conditional allele ﬂanked with site-specific recombinase target sequences; (i) insertion of a selectable marker or a reporter gene operably linked to a third promoter active in the mammalian cell; or (1') a combination thereof. In one embodiment, the target genomic locus comprises (i) a 5’ target sequence that is homologous to a 5’ gy arm; and (ii) a 3’ target sequence that is homologous to a 3’ homology arm.

In one embodiment, the 5’ target sequence and the 3’ target sequence is separated by at least kb but less than 3 Mb. In one embodiment, the 5’ target sequence and the 3’ target sequence is separated by at least 5 kb but less than 10 kb, at least 10 kb but less than 20 kb, at least 20 kb but less than 40 kb, at least 40 kb but less than 60 kb, at least 60 kb but less than 80 kb, at least about 80 kb but less than 100 kb, at least 100 kb but less than 150 kb, or at least 150 kb but less than 200 kb, at least about 200 kb but less than about 300 kb, at least about 300 kb but less than about 400 kb, at least about 400 kb but less than about 500 kb, at least about 500 kb but less than about le, at least about 1 Mb but less than about 1.5 Mb, at least about 1.5 Mb but less than about 2 Mb, at least about 2 Mb but less than about 2.5 Mb, or at least about 2.5 Mb but less than about 3 Mb. In one embodiment, the first and the second expression constructs are on a single nucleic acid molecule. In one embodiment, the target genomic locus comprises the Sry locus.

Further provided is a method for targeted genetic modification on the Y chromosome of a non-human animal, comprising: (a) modifying a genomic locus of interest on the Y chromosome of a non-human pluripotent cell according to the methods described herein, y producing a genetically modified non-human pluripotent cell comprising a targeted genetic modification on the Y some; (b) introducing the ed non- human pluripotent cell of (a) into a non-human host embryo; and gestating the non-human host embryo comprising the modified pluripotent cell in a surrogate mother, wherein the surrogate mother produces F0 progeny comprising the ed genetic modification, wherein the ed genetic modification is e of being transmitted through the germline. In one embodiment, the genomic locus of interest comprises the Sry locus.

Methods and compositions are provided for generating targeted genetic modifications on the Y chromosome. Compositions include an in vitro culture comprising an XY pluripotent and/or totipotent animal cell (i.e., XY ES cells or XY iPS cells) having a modification that decreases the level and/or activity of an Sry protein; and, culturing these cells in a medium that promotes development of XY F0 fertile s. Such compositions find use in various methods for making a fertile female XY non-human s in an F0 generation.

BRIEF DESCRIPTION OF THE FIGURES provides a schematic of the CRISPR Cas9/gRNA targeting the mouse Sry gene. VG-l (SEQ ID NO:10); VG-2 (SEQ ID NO:1 l); VG-3 (SEQ ID NO:12). The primers and probes indicated in are provided in SEQ ID NOS: 13-29. provides a schematic of ing the Sry gene with TALEN and CRISPR using a lacZ reporter gene. The Sry gene was targeted with both a LTVEC and a armed vector (smallTVEC) having homology arms smaller than a LTVEC in order to avoid nging loci on the Y chromosome. rates LacZ sion in embryos. provides a schematic of a large deletion of greater than 500 kb on the Y chromosome mediated by ZFNs or by CRISPR guide RNAs in combination with Cas9 DNA endonuclease.

A, B, and C provides the sequencing confirmation of the large Y chromosome on in various clones. A is the sequencing result for clone l-D5. The Kdm5 Up and Uspy9 down sequence is provided in SEQ ID NO:30; l-D5 l500F (SEQ ID NO:3l); l-D5 1000R (SEQ ID NO:32); is the sequencing result for clone 5-C4. The 2015/038001 Kdm5 Up and Uspy9 down sequence is provided in SEQ ID NO:33; l500F (SEQ ID NO:34); 1000R (SEQ ID NO:35); 1000F (SEQ ID N036); and is the sequencing result for clone 6-Al2. The Kde Up and Uspy9 down sequence is provided in SEQ ID NO:37; l500F (SEQ ID N038); 1000R (SEQ ID NO:39); 1000F (SEQ ID NO:40); 1500R (SEQ ID . The boxed regions in and represent micro-homology regions.

DETAILED DESCRIPTION DEFINITIONS The terms “protein,” “polypeptide,” and “peptide,” used interchangeably herein, e polymeric forms of amino acids of any length, including coded and non-coded amino acids and chemically or biochemically modified or derivatized amino acids. The terms also include polymers that have been modified, such as polypeptides having modified peptide backbones.

The terms “nucleic acid” and “polynucleotide,” used interchangeably herein, include ric forms of tides of any length, including ribonucleotides, deoxyribonucleotides, or analogs or modified versions thereof. They e single-, double- and multi-stranded DNA or RNA, genomic DNA, cDNA, DNA-RNA hybrids, and polymers comprising purine bases, pyrimidine bases, or other natural, chemically modified, biochemically ed, non-natural, or derivatized nucleotide bases. For simplicity, nucleic acid size may be referred to in bp whether the nucleic acid is in double-or single-stranded form, in the latter case, the bp being those formed if and when the single-stranded nucleic acid is duplexed with its exactly complementary strand.

“Codon optimization” generally includes a process of modifying a nucleic acid sequence for enhanced expression in particular host cells by replacing at least one codon of the native sequence with a codon that is more frequently or most frequently used in the genes of the host cell while maintaining the native amino acid ce. For example, a nucleic acid encoding a Cas protein can be modified to substitute codons having a higher frequency of usage in a given prokaryotic or otic cell, including a bacterial cell, a yeast cell, a human cell, a non-human cell, a mammalian cell, a rodent cell, a mouse cell, a rat cell, a hamster cell, or any other host cell, as compared to the naturally occurring nucleic acid ce. Codon usage tables are readily available, for e, at the “Codon Usage se.” These tables can be adapted in a number of ways. See Nakamura et a1. (2000) Nucleic Acids Research 28:292. Computer thms for codon optimization of a particular sequence for expression in a particular host are also available (see, e. g., Gene Forge).

“Operable linkage” or being “operably linked” includes juxtaposition of two or more components (e.g., a promoter and another sequence element) such that both ents function normally and allow the ility that at least one of the components can mediate a function that is exerted upon at least one of the other components. For example, a promoter can be operably linked to a coding sequence if the promoter controls the level of transcription of the coding sequence in response to the ce or absence of one or more transcriptional regulatory factors.

“Complementarity” of nucleic acids means that a nucleotide sequence in one strand of c acid, due to orientation of its nucleobase groups, forms hydrogen bonds with another sequence on an opposing nucleic acid strand. The complementary bases in DNA are typically A with T and C with G. In RNA, they are typically C with G and U with A. mentarity can be t or substantial/sufficient. Perfect complementarity between two c acids means that the two nucleic acids can form a duplex in which every base in the duplex is bonded to a complementary base by Watson-Crick pairing. "Substantial" or "sufficient" complementary means that a sequence in one strand is not tely and/or perfectly complementary to a sequence in an opposing strand, but that sufficient bonding occurs between bases on the two strands to form a stable hybrid complex in set of hybridization conditions (e.g., salt concentration and temperature). Such conditions can be predicted by using the sequences and standard mathematical calculations to t the Tm of ized strands, or by empirical determination of Tm by using routine methods. Tm includes the temperature at which a population of hybridization complexes formed between two c acid strands are 50% denatured. At a temperature below the Tm, ion of a hybridization complex is favored, whereas at a temperature above the Tm, melting or separation of the strands in the hybridization complex is favored. Tm may be estimated for a nucleic acid having a known G+C t in an aqueous l M NaCl solution by using, e. g., Tm=81.5+0.4l(% G+C), although other known Tm computations take into account nucleic acid structural characteristics.

"Hybridization condition" es the cumulative environment in which one nucleic acid strand bonds to a second nucleic acid strand by complementary strand interactions and hydrogen bonding to produce a hybridization complex. Such conditions include the chemical components and their concentrations (e. g., salts, chelating agents, formamide) of an aqueous or organic solution containing the nucleic acids, and the temperature of the mixture. Other s, such as the length of tion time or reaction chamber dimensions may contribute to the environment. See, e. g., Sambrook et al., Molecular Cloning, A Laboratory Manual, 2.sup.nd ed., pp. 1.90-1.91, 9.47-9.51, 1 1.47- 1157 (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).

Hybridization requires that the two nucleic acids contain complementary ces, although mismatches between bases are le. The conditions appropriate for hybridization between two nucleic acids depend on the length of the nucleic acids and the degree of complementation, variables well known in the art. The greater the degree of complementation between two nucleotide sequences, the greater the value of the melting temperature (Tm) for hybrids of nucleic acids having those sequences. For hybridizations between nucleic acids with short stretches of complementarity (e.g. complementarity over 35 or fewer, 30 or fewer, 25 or fewer, 22 or fewer, 20 or fewer, or 18 or fewer nucleotides) the on of ches becomes important (see Sambrook et al., supra, 11.7-11.8).

Typically, the length for a izable nucleic acid is at least about 10 nucleotides.

Illustrative minimum lengths for a hybridizable c acid include at least about 15 nucleotides, at least about 20 nucleotides, at least about 22 nucleotides, at least about 25 nucleotides, and at least about 30 nucleotides. Furthermore, the temperature and wash solution salt concentration may be adjusted as ary according to factors such as length of the region of complementation and the degree of complementation.

The sequence of polynucleotide need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable. Moreover, a polynucleotide may hybridize over one or more segments such that ening or adjacent segments are not involved in the hybridization event (e. g., a loop structure or hairpin structure). A polynucleotide (e. g., gRNA) can comprise at least 70%, at least 80%, at least 90%, at least 95%, at least 99%, or 100% sequence complementarity to a target region within the target nucleic acid sequence to which they are targeted. For e, a gRNA in which 18 of 20 nucleotides are complementary to a target region, and would therefore specifically hybridize, would represent 90% complementarity. In this example, the remaining noncomplementary nucleotides may be clustered or persed with mentary nucleotides and need not be contiguous to each other or to complementary nucleotides.

Percent complementarity between particular stretches of nucleic acid sequences within c acids can be determined routinely using BLAST programs (basic local alignment search tools) and PowerBLAST programs known in the art (Altschul et a1. (1990) J. M01. Biol. 215:403-410; Zhang and Madden (1997) Genome Res. 656) or by using the Gap m (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, n Wis.), using default settings, which uses the algorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2, 482-489).

The methods and compositions provided herein employ a variety of different components. It is recognized hout the description that some components can have active variants and fragments. Such components include, for example, Cas proteins, CRISPR RNAs, trachNAs, and guide RNAs. Biological activity for each of these components is described elsewhere herein. nce identity" or "identity" in the context of two polynucleotides or polypeptide sequences makes reference to the residues in the two sequences that are the same when aligned for maximum correspondence over a specified comparison window. When percentage of sequence identity is used in nce to proteins it is recognized that residue positions which are not identical often differ by conservative amino acid substitutions, where amino acid residues are substituted for other amino acid es with similar chemical properties (e. g., charge or hydrophobicity) and therefore do not change the functional properties of the molecule. When ces differ in vative substitutions, the percent sequence identity may be adjusted upwards to correct for the conservative nature of the substitution. Sequences that differ by such conservative substitutions are said to have nce similarity" or "similarity." Means for making this adjustment are well known to those of skill in the art. Typically, this involves scoring a conservative substitution as a partial rather than a full mismatch, thereby increasing the percentage sequence identity.

Thus, for example, where an identical amino acid is given a score of 1 and a non-conservative substitution is given a score of zero, a conservative substitution is given a score between zero and 1. The scoring of conservative substitutions is calculated, e. g., as implemented in the program PC/GENE (Intelligenetics, Mountain View, California).

"Percentage of sequence identity" includes the value determined by comparing two lly aligned ces over a comparison , wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) as ed to the reference sequence (which does not se additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid base or amino acid residue occurs in both ces to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison, and multiplying the result by 100 to yield the percentage of ce identity. 2015/038001 Unless otherwise stated, sequence ty/similarity values include the value obtained using GAP Version 10 using the following parameters: % identity and % similarity for a nucleotide sequence using GAP Weight of 50 and Length Weight of 3, and the nwsgapdna.cmp scoring matrix; % identity and % similarity for an amino acid sequence using GAP Weight of 8 and Length Weight of 2, and the BLOSUM62 scoring matrix; or any equivalent program f. "Equivalent program" includes any sequence comparison m that, for any two ces in question, generates an alignment having identical nucleotide or amino acid residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.

Compositions or methods “comprising” or “including” one or more recited ts may include other elements not specifically recited. For example, a composition that “comprises” or “includes” a protein may contain the protein alone or in combination with other ingredients.

Designation of a range of values includes all integers within or defining the range, and all subranges defined by integers within the range.

Unless ise apparent from the context, the term “about” encompasses values within a standard margin of error of measurement (e. g., SEM) of a stated value.

The singular forms of the articles “a,” “an,” and “the” include plural references unless the context clearly dictates ise. For example, the term “a Cas protein” or “at least one Cas protein” can e a plurality of Cas proteins, including mixtures f. 1. Methods and itions to Make a Fertile Female XY Animal in an F0 Generation Methods for making non-human animals from donor ES cells and host embryos are known. Donor ES cells are selected for certain characteristics that enhance the ability of the cells to populate a host embryo and thus contribute in part or in substantial part to an animal formed by the donor ES cells and the host embryo. The animal formed may be male or female, based in large part on the genotype of the ES cell (e. g., XY or XX).

The ty of ES cell lines for making transgenic animals have a male XY genotype. e of the dominance of the Y chromosome in mammalian sex determination, when XY ES cells are introduced into a blastocyst host embryo and gestated, they nearly always produce in the first generation (F0) phenotypically male animals that are chimeras, i.e., that contain cells derived from the male donor ES cell (XY) and cells derived from the host embryo, which can be either male (XY) or female (XX). XY ES cells, when introduced 2015/038001 into an 8-cell host embryo by the Mouse method and gestated, can produce in the first generation (F0) phenotypically male animals that are fully derived from the XY ES cells.

W0201 1/156723 es s and compositions which employ a culture media for maintaining XY donor cells in culture such that after introduction of the XY donor cells into a host embryo and gestation in a suitable host, fertile XY female animals are produced in the F0 population. Such compositions find use in making Fl progeny that are homozygous for the given targeted genetic modification.

The instant application provides s and compositions that employ a combination of XY donor cells having a modification that decreases the level and/or activity of the Sry protein in combination with a culture media that promotes the production of anatomically normal, e and fecund, XY F0 females. Such s and compositions allow for making a fertile female XY man animal in an F0 generation. The combination of XY ES cells having a modification that decreases the level and/or activity of the Sry protein in combination with the culture media described herein significantly increases the percentage of fertile female XY y in the F0 generation. Methods for the ent male to female sex conversion are valuable to the domestic animal industry. For example, female calves are much more valuable to the dairy cattle industry than males. The same is true for poultry. For breeding es, whether it be cattle or hogs or sheep, it is preferred to breed many females to only a few bulls, boars, or rams. Thus, the various methods provided herein find use in various commercially important breeding industries.

Methods and compositions are also provided for making a XY embryonic stem (ES) cell line capable of producing a fertile XY female man mammal in an F0 generation without culturing in a feminizing media. In such methods, the XY ES cell line having a modification that decreases the level and/or activity of an Sry protein can produce an ES cell line capable of producing a fertile XY female non-human mammal in an F0 generation in the absence of a feminizing media provided elsewhere herein (e. g., by culturing in a base medium, such as DMEM, described elsewhere herein).

A. Animal XY Cells Having a Modification that Decreases the Level and/or Activity of an Sry Protein Various itions and methods are provided herein which comprise various XY pluripotent and/or totipotent cells from an animal. The term “pluripotent cell” as used herein es an undifferentiated cell that possesses the ability to develop into more than one differentiated cell types. Such pluripotent and/or totipotent XY cells can be, for example, an embryonic stem (ES) cell or an induced pluripotent stem (iPS) cell. The term "embryonic stem cell" or "ES cell" as used herein includes an -derived totipotent or pluripotent cell that is capable of contributing to any tissue of the developing embryo upon introduction into an embryo.

The term "animal," in reference to cells, pluripotent and/or totipotent cells, XY cells, ES cells, iPS cells, donor cells and/or host embryos, includes mammals, fishes, and birds. Mammals include, e. g., humans, non-human es, monkey, ape, cat dog, horse, bull, deer, bison, sheep, rodents (e. g., mice, rats, hamsters, guinea pigs), livestock (e. g., bovine species, e. g., cows, steer, etc.; ovine species, e. g., sheep, goats, etc.; and porcine species, e.g., pigs and boars). Birds e, e.g., chickens, turkeys, ostrich, geese, ducks, etc. icated animals and agricultural animals are also included. The phrase "non-human animal," in reference to cells, XY cells, ES cells, donor cells and/or host embryos, excludes humans.

In specific embodiments, the pluripotent cell is a human XY ES cell, a human XY iPS cell, a human adult XY ES cell, a developmentally cted human progenitor ES cell, a non-human XY ES cell, a non-human XY iPS cell, a rodent XY ES cell, a rodent XY iPS cell, a mouse XY ES cell, a mouse XY iPS cell, a rat XY ES cell, a rat XY iPS cell, a hamster XY ES cell, a hamster XY iPS cell, a monkey XY ES cell, a monkey XY iPS cell, an agricultural mammal XY ES cell, an agricultural XY iPS cell, a domesticated mammal XY ES cell, or a domesticated XY iPS cell. Moreover, the XY ES cell or the XY iPS cell can be from an inbred strain, a hybrid strain or an outbred strain. It is further recognized that the pluripotent and/or totipotent XY cells can comprise an XYY karyotype or an XXY ype.

Mouse pluripotent and/or totipotent cells (i.e., XY ES cells or XY iPS cells) can be from a 129 strain, a C57BL/6 strain, a mix of 129 and C57BL/6, a BALB/c strain, or a Swiss Webster strain. In a specific embodiment, the mouse is 50% 129 and 50% C57BL/6.

In one embodiment, the mouse is a 129 strain selected from the group consisting of a strain that is 129P1 , 129P2, 129P3, 129X1 , 129S1 (e.g., 129S1/SV, 129S1/Svlm), 129S2, 129S4, 129S5, 129S9/SvaH, 129S6 (129/SvaTac), 129S7, 129S8, 129T1 , 129T2. See, for example, Festing et al. (1999) Mammalian Genome 10:836). In one embodiment, the mouse is a C57BL strain, and in a specific embodiment is from C57BL/A, C57BL/An, GrFa, C57BL/Kal_wN, C57BL/6, 6J, C57BL/6ByJ, C57BL/6NJ, C57BL/6NTac, C57BL/10, C57BL/10ScSn, C57BL/10Cr, or C57BL/Ola. In a ic embodiment, the mouse is a mix of an entioned 129 strain and an aforementioned C57BL/6 strain. In another specific embodiment, the mouse is a mix of aforementioned 129 s, or a mix of aforementioned BL/6 strains. In a specific embodiment, the 129 strain of the mix is a 129S6 (129/SvaTac) strain. In some embodiments, the mouse XY ES cell comprises a Y some derived from the 129 strain.

In yet another embodiment, the XY mouse ES cell is a VGF1 mouse ES cell.

VGF1 (also known as F1H4) mouse ES cells were derived from hybrid embryos produced by ng a female C57BL/6NTac mouse to a male 129S6/SvaTac mouse. Therefore, VGF1 ES cells contain a Y chromosome from 129S6/SvaTac mouse. See, for example, Auerbach, W. et a1. (2000) Establishment and chimera analysis of 129/Sva- and C57BL/6-derived mouse embryonic stem cell lines. Biotechniques 29, 1024—1028, 1030, 1032, herein incorporated by reference in its ty.

A rat pluripotent and/or totipotent cell (i.e., XY ES cell or XY iPS cell) can be from any rat strain, including but not limited to, an ACI rat strain, a Dark Agouti (DA) rat strain, a Wistar rat strain, a LEA rat strain, a Sprague Dawley (SD) rat strain, or a Fischer rat strain such as Fisher F344 or Fisher F6. Rat pluripotent and/or totipotent cells (i.e., XY ES cells or XY iPS cells) can also be obtained from a strain derived from a mix of two or more strains recited above. In one embodiment, the rat pluripotent and/or totipotent cell (i.e., XY ES cell or XY iPS cell) is derived from a strain selected from a DA strain and an ACI strain.

In a specific embodiment, the rat otent and/or totipotent cell (i.e., XY ES cell or XY iPS cell) is derived from an ACI strain. The ACI rat strain is characterized as having black agouti, with white belly and feet and an RT] haplotype. Such s are available from a variety of sources including Harlan Laboratories. In other embodiments, the various rat pluripotent and/or totipotent cell (i.e., XY ES cell or XY iPS cell) are from a Dark Agouti (DA) rat strain, which is characterized as having an agouti coat and an RT] ype.

Such rats are available from a variety of sources including Charles River and Harlan Laboratories. In a further embodiment, the rat pluripotent and/or tent cells (i.e., XY ES cells or XY iPS cells) are from an inbred rat strain. In specific embodiments the rat ES cell line is from an ACI rat and comprises the ACI.G1 rat ES cell. In another ment, the rat ES cell line is from a DA rat and comprises the DA.2B rat ES cell line or the DA.2C rat ES cell line. See, for example, US. Utility Application No. 14/185,703, filed on ry 20, 2014 and herein incorporated by nce in its entirety.

In s embodiments, the pluripotent and/or totipotent cell (i.e., XY ES cell or XY iPS cell), the donor cell and/or the host embryo are not from one or more of the following: Akodon spp., Myopus spp., Microtus spp., Talpa spp. In various embodiments, the donor cell and/or the host embryo are not from any species of which a normal wild-type characteristic is XY female fertility. In various embodiments, where a genetic modification is present in the pluripotent and/or totipotent cell (i.e., XY ES cell or XY iPS cell), the donor cell or the host embryo, the genetic modification is not an XYY or XXY, a Tdy-negative sex reversal, Tdy-positive sex reversal, an X0 modification, an aneuploidy, an fgf9'/' genotype, or a SOX9 modification.

The pluripotent and/or totipotent XY cells (i.e., an XY ES cell or an XY iPS cell) employed in the methods and compositions have a genetic modification that results in a decreased level and/or activity of the Sry protein. The “Sex Determining Region Y” n or the “Sry” n is a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. Sry is the testis-determining factor that initiates male sex determination. The sequence of the Sry protein from a variety of sms is known, including from mouse (Accession No. Q05738); rat (GenBank: CAA61882.1) human (Accession No. Q05066); cat (Accession No. Q67C50), and horse (Accession No.

P36389), each of which is herein incorporated by reference.

In general, the level and/or activity of the Sry protein is decreased if the protein level and/or the activity level of the Sry protein is statistically lower than the protein level of Sry in an appropriate l cell that has not been genetically ed or mutagenized to inhibit the sion and/or activity of the Sry protein. In specific embodiments, the concentration and/or activity of the Sry n is decreased by at least 1%, 5%, 10%, 20%, %, 40%, 50%, 60%, 70%, 80%, or 90% relative to a control cell which has not been modified to have the decreased level and/or activity of the Sry protein.

A ct cell” is one in which a genetic tion, such as a genetic modification disclosed herein has been effected, or is a cell which is descended from a cell so d and which comprises the alteration. A “control” or “control cell” provides a reference point for measuring changes in phenotype of the subject cell. In one embodiment, a control cell is as closely matched as possible with the cell with reduced Sry activity except it lacks the genetic modification or mutation resulting in the d activity (for example, the respective cells can originate from the same cell line). In other instances, the control cell may comprise, for example: (a) a wild-type cell, i.e., of the same genotype as the ng material for the genetic alteration which resulted in the subject cell; (b) a cell of the same genotype as the starting material but which has been genetically modified with a null uct (i.e. with a construct which has no known effect on the trait of st, such as a construct comprising a marker gene); (c) a cell which is a non-genetically modified progeny of a subject cell (i.e., the control cell and the t cell originate from the same cell line); (d) a cell genetically identical to the subject cell but which is not exposed to ions or stimuli that would induce expression of the gene of interest; or (e) the subject cell itself, under conditions in which the genetic cation does not result in an alteration in expression of the polynucleotide of interest.

The expression level of the Sry polypeptide may be measured directly, for e, by assaying for the level of the Sry polypeptide in the cell or organism, or indirectly, for example, by measuring the activity of the Sry polypeptide. Various methods for determining the activity of the Sry protein are known. See, Wang et a1. (2013) Cell 153:910-918, Mandalos et a1. (2012) PLOS ONE 7:e45768:1-9, and Wang et al. (2013) Nat Biotechnol. 31:530-532, each of which is herein incorporated by reference.

In other instances, cells having the targeted genetic modification that reduces the activity and/or level of the Sry polypeptide are selected using methods that include, but are not limited to, Southern blot is, DNA sequencing, PCR is, or phenotypic analysis. Such cells are then employed in the s methods, compositions and kits described herein.

A targeted genetic modification can comprise a targeted alteration to a cleotide of interest including, for example, a targeted alteration to a target genomic locus on the Y chromosome, a ed alteration to the Sry gene, or a targeted alteration to other desired polynucleotides. Such ed modifications include, but are not limited to, additions of one or more tides, deletions of one or more nucleotides, substitutions of one or more nucleotides, a knockout of the polynucleotide of interest or a portion thereof, a knock-in of the polynucleotide of interest or a portion thereof, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence, or a combination thereof. In ic embodiments, at least 1, 2, 3, 4, 5, 7, 8, 9, 10 or more nucleotides are changed to form the targeted genomic cation.

A decrease in the level and/or activity of the Sry protein can result from a genetic modification in the Sry gene (i.e., a genetic modification in a regulatory region, the coding region, and/or introns etc). Such genetic modifications include, but are not limited to, additions, deletions, and substitutions of nucleotides into the genome. Such genetic modifications can e an alteration of the Sry gene, including, for example, an insertion of one or more nucleotides into the Sry gene, a deletion of one or more nucleotides from the Sry gene, a substitution of one or more nucleotides in the Sry gene, a knockout of the Sry gene or a portion thereof, a n of the Sry gene or a portion thereof, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence, or a combination thereof. Thus, in specific embodiments, the activity of an Sry polypeptide may be reduced or eliminated by disrupting the gene encoding the Sry polypeptide. In specific embodiments, at least 1, 2, 3, 4, 5, 7, 8, 9, 10 or more nucleotides are d in the Sry gene. s methods can be used to generate the additional targeted genetic modification.

See, for example, Wang et a1. (2013) Cell 153:910-918, Mandalos et a1. (2012) PLOS ONE 7:e45768:1-9, and Wang et al. (2013) Nat Biotechnol. 31:530-532, each of which is herein incorporated by reference. In on, the various s described herein to modify genomic locus on the Y chromosome can be used to introduce targeted genetic modification to the Sry gene.

In other embodiments, the activity and/or level of the Sry polypeptide is reduced or eliminated by introducing into the cell a polynucleotide that ts the level or activity of the Sry polypeptide. The polynucleotide may inhibit the expression of the Sry polypeptide directly, by preventing translation of the Sry messenger RNA, or indirectly, by encoding a polypeptide that inhibits the transcription or translation of the gene encoding an Sry protein.

In other embodiments, the activity of Sry polypeptide is reduced or eliminated by introducing into the cell a ce encoding a polypeptide that inhibits the activity of the Sry polypeptide.

In one embodiment, the XY otent and/or totipotent cells (i.e., XY ES cell or XY iPS cell) comprise a conditional Sry allele that reduces the activity and/or level of the Sry protein. A “conditional Sry allele” includes a modified Sry gene designed to have the decreased level and/or activity of the Sry protein at a desired developmental time and/or within a d tissue of st. Reduced level and/or activity can be compared with a control cell lacking the modification giving rise to the conditional allele, or in the case of d activity at a desired developmental time with ing and/or following times, or in the case of a desired tissue, with a mean activity of all tissues. In one embodiment, the conditional Sry allele comprises a ional null allele of Sry that can be switch off at a d developmental time point and/or in specific tissues. Such a conditional allele can be used to create fertile XY females derived from any gene-targeted clone. As described elsewhere herein, such a method enables the creation of a desired homozygous genetic modification in the F1 generation. Such methods provide a quick look at the phenotype t having to breed to the F2 generation.

In a non-limiting embodiment, the conditional Sry allele is a multifunctional , as described in US 2011/0104799, which is incorporated by reference in its entirety. 2015/038001 In specific embodiments, the conditional allele comprises: (a) an actuating sequence in sense orientation with t to transcription of a target gene, and a drug selection cassette (DSC) in sense or antisense orientation; (b) in antisense orientation a nucleotide sequence of st (NSI) and a conditional by inversion module (COIN, which utilizes an exon-splitting intron and an invertible genetrap-like module; see, for example, US 2011/0104799, which is incorporated by reference in its entirety); and (c) recombinable units that recombine upon exposure to a first recombinase to form a conditional allele that (i) lacks the actuating ce and the DSC, and (ii) contains the NSI in sense orientation and the COIN in antisense ation.

The conditional allele of the Sry gene can be ted in any cell type, and is not limited to an XY pluripotent and/or totipotent cell. Such cells types along with non-limiting methods to target a genomic locus on the Y chromosome are discussed in further detail elsewhere herein.

As discussed elsewhere herein, the pluripotent and/or totipotent XY cell (i.e., an XY ES cell or an XY iPS cell) having genetic modification that decreases the level and/or activity of the Sry protein can further comprise at least one onal targeted genetic modification to a polynucleotide of st. The at least one onal targeted genetic cation can comprise a substitution of one or more nucleic acids, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence, a knockout, and a knock-in. The additional targeted genetic modification can be on the Y chromosome, the X chromosome or on an autosome. Various s can be used to generate the onal targeted genetic modification, including employing targeting plasmids and large targeting vectors as discussed ere herein. See, also, [[820080092249, WG/1999/005266A2, USEOOL’EQIWZ’éS’O, WO/2008/017234Al, and US Patent No. 7,612,250, each of which is herein incorporated by reference, for methods related to nuclear transfer. In addition, the various methods described herein to modify genomic locus on the Y chromosome (i.e., the Sry gene) can also be used to introduce targeted genetic modifications to polynucleotides of interest that are not d on the Y chromosome.

B. Mediafor Culturing the Pluripotent and/or Totipotent XY Cells Having a Modification that Decreases the Level and/or Activity ofan Sry Protein The culture media employed in the various s and compositions that promote XY fertile female in the F0 generation is such that it maintains the pluripotent and/or totipotent cells (i.e., ES cell, iPS cells, XY ES cells, XY iPS cells, etc.). The terms WO 00805 “maintain77 ll , ining" and "maintenance" refer to the stable preservation of at least one or more of the characteristics or phenotypes of pluripotent and/or totipotent cells described herein ding ES cells or iPS cells). Such ypes can e maintaining pluripotency and/or totipotency, cell morphology, gene expression profiles and the other functional characteristics of the cells. The terms “maintain”, "maintaining" and "maintenance" can also encompass the propagation of cells, or an increase in the number of cells being cultured. The terms further contemplate culture conditions that permit the cells to remain pluripotent, while the cells may or may not continue to divide and increase in number.

In some embodiments, the XY cells having the genetic modification that reduces the level and/or activity of the Sry protein are maintained by ing in any base medium known in the art (e. g., DMEM) that is suitable for use (with added supplements) in growing or maintaining the pluripotent and/or totipotent cells (i.e., ES cell, iPS cells, XY ES cells, XY iPS cells, etc.) in culture. In such cases, the cultured XY ES cells have the potential to develop into fertile female animals but still retain pluripotency and/or totipotency, such that the cells can be implemented into a recipient embryo and give rise to a fertile female progeny.

In other embodiments, XY cells having the c modification that s the level and/or activity of the Sry n are maintained by culturing in a medium as further defined below for sufficient time that some of the cells convert to KY cells with the potential to develop into fertile female animals but still retain pluripotency and/or totipotency, such that the cells can be implemented into a recipient embryo and give rise to a fertile female progeny.

The medium employed to maintain the XY pluripotent and/or totipotent cells (i.e., XY ES cells, XY iPS cells, etc.) having the genetic modification that reduces the level and/or activity of the Sry protein promotes the pment of XY F0 fertile females. Thus, ing in such a medium increases the number of XY F0 e females that are obtained when compared to culturing in an appropriate control medium (such as, for example, one based on DMEM). Thus, an increased number of XY F0 fertile females can comprise at least %, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% of the F0 non-human animals (following introduction of the non-human animal XY ES cells into a host embryo and gestation of the host embryo) are XY females and which upon attaining sexual maturity the F0 XY female non-human animal is fertile.

The phrase "base medium" or "base media" es, for example, a base medium known in the art (e. g., DMEM) that is suitable for use (with added ments) in growing or ining the pluripotent and/or totipotent cells (i.e., ES cell, iPS cells, XY ES cells, XY iPS cells, etc.) in culture. Base media suitable for making a fertile XY female (i.e., "low-salt DMEM" or “low-osmolality medium”) differs from base media typically used to maintain ES cells in culture. For purposes of discussing base media in general, base media that are not suitable for making fertile XY females are described in this section as "DMEM" and in Table 1 (e. g., typical DMEM media). For purposes of discussing base media suitable for making fertile XY females, the phrase "low-salt DMEM" or “low-osmolality DMEM” is used.

Differences between base media typically used to maintain pluripotent and/or totipotent cells in culture (e. g., DMEM) and base media suitable for making fertile XY females (e. g., "low- salt DMEM") are articulated herein. The phrase "low-salt DMEM" is used for convenience; suitable DMEM for making e XY females exhibits characteristics not limited to "low- salt," but includes those bed herein. For example, the DMEM shown in Table 1 can be made suitable for making fertile XY females by altering the sodium de and/or sodium bicarbonate concentrations as provided for herein, which will also result in a different osmolality and a different conductivity as compared with the DMEM shown in Table 1. An example of base medium is Dulbeco's ed Eagle's Medium (DMEM), in various forms (e. g., ogen DMEM, Cat. No. 1 1971 -025) (Table 1). A suitable low-salt DMEM is available commercially as KO-DMEMTM (Invitrogen Cat. No. 10829-018). Base medium is lly supplemented with a number of supplements known in the art when used to maintain cells in e for use as donor cells. Such supplements are indicated as "supplements" or "+ supplements" in this disclosure.

Table 1 : DMEM Base Media for Maintaining or Culturing Pluripotent and/or Totipotent Cells Component Mg/L mM Glycine 30 0.4 L-Arginine0HCI 84 0.398 L-Cystine02HCI 63 0.201 L-Glutamine 584 4 L—Histidine-HCI-H2O 42 0.2 L—Isoleucine 105 0.802 L-Leucine 105 0.802 L-Lysine0HCI 146 0.798 L-Methionine 30 0.201 L-Phenylalanine 66 0.4 L-Serine 42 0.4 L—Threonine 95 0.798 tophan 16 0.0784 L-Tyrosine um salt dihydrate 104 0.398 ne 94 0.803 e chloride 4 0.0286 D-Calcium pantothenate 4 8.39 X 10'3 Folic Acid 4 9.07 x 10'3 Niacinamide 4 0.0328 Pyridoxine°HCI 4 0.0196 Riboﬂavin 0.4 1.06 x 10'3 Thiamine°HCI 4 0.0119 i-Inositol 7.2 0.04 Calcium Chloride (CaClz) (anhydrous) 200 1.8 Ferric Nitrate (Fe(N03)3.9HzO) 0.1 2.48 x 10-4 Magnesium Sulfate (MgSO4) (anhyd.) 97.67 0.814 Potassium Chloride (KCI) 400 5.33 D-Glucose (Dextrose) 4500 25 Phenol Red 15 0.0399 NaCL/NaHCO3 Content of DMEM Sodium onate (NaHCOg) 3700 44.05 Sodium Chloride (NaCl) 6400 110.34 NaCl/NaHCO3 Content of Low-salt DMEM Sodium Bicarbonate (NaHCOg) <3700 <44.05 Sodium Chloride (NaCl) <6400 <110.34 The term "supplements" or the phrase "+ supplements," includes elements added to base medium for growing or maintaining pluripotent and/or totipotent cells (i.e., XY ES cell or XY iPS cells) in culture, e. g., for maintaining pluripotency or totipotency of donor cells in culture. For example, media supplements suitable for growing or maintaining otent and/or totipotent cells in culture e, but are not limited to, fetal bovine serum (FBS), glutamine, antibiotic(s), penicillin and streptomycin (e. g., penstrep), pyruvate salts (e. g., sodium pyruvate), nonessential amino acids (e. g., MEM NEAA), 2-mercaptoethanol, and Leukemia Inhibitory Factor (LIF).

In one embodiment, the base medium comprises one or more supplements le for maintaining pluripotent cells in culture, including for example, XY ES cells or XY iPS cells having a reduced capacity to contribute to the male sex determination developmental program after injection into an embryo and intrauterine er to a surrogate mother mouse.

In a specific embodiment, the one or more ments suitable for maintaining the pluripotent cell in e are PBS (90 ml PBS/0.5L base medium), glutamine (2.4 mmoles/0.5 L base medium), sodium pyruvate (0.6 mmoles/0.5L base medium), nonessential amino acids (< 0.1 mmol/0.5 L base medium), 2-mercaptoethanol, LIF, and one or more antibiotics.

In other embodiments, the media for maintaining pluripotent cells in culture, including for example, XY ES cells or XY iPS cells having a reduced capacity to contribute to the male sex ination developmental program after injection into an embryo and intrauterine transfer to a surrogate mother mouse, comprises about 500 ml of base medium in which the ing supplements are added: about 90 ml FBS (e.g., Hylcone FBS Cat. No.

SH30070.03), about 2.4 millimoles of glutamine (e. g., about 12 ml of a 200 mM glutamine solution, e. g., Invitrogen Cat. No. 081, penicillin:streptomycin (e. g., 60,000 units of Penicillin G sodium and 60 mg of streptomycin sulfate, with about 51 mg of NaCl; e. g., about 6 ml. of Invitrogen pennstrep, Cat. No. 15140-122), about 0.6 millimoles of sodium pyruvate (e. g., 6 ml. of 100 mM sodium pyruvate, Invitrogen Cat. No. 1 1360-070), about 0.06 oles of ential amino acids (e. g., about 6 ml. of MEM NEAA, e. g., MEM NEAA from Invitrogen Cat. No. 1 1 140-050), about 1.2 ml. 2-mercaptoethanol, and about 1.2 micrograms of LIF (e.g., about 120 microliters of a 106 units/mL LIF preparation; e. g., about 120 microliters of Millipore ESGROTM-LIF, Cat. No. ESGl 107). When composing base media for maintaining XY ES or XY iPS cells for making e XY females, lly the same supplements in about the same amounts are employed, but the composition of the base medium will differ (from DMEM, e.g., from the medium described in the table above) and the difference(s) correspond to the difference(s) taught herein.

In some embodiments, ments include Wnt-conditioned media, e.g., Wnt-3a conditioned media.

In one embodiment, the pluripotent cell, including for example, an XY ES cell or an XY iPS cell having a reduced capacity to contribute to the male sex determination developmental program after injection into an embryo and intrauterine transfer to a surrogate mother mouse, is maintained in an in vitro culture in a medium sing base medium and supplements, wherein the base medium exhibits one or more of the following characteristics: (a) an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg; (b) a conductivity of about 11 mS/cm to about 13 mS/cm; (C) a salt of an alkaline metal and a halide in a concentration of about 50mM to about 110 mM; (d) a carbonic acid salt concentration of about 17mM to about 30 mM; (e) a total ne metal halide salt and carbonic acid salt concentration of about 85mM to about 130 mM; and/or (f) a combination of any two or more thereof. In other embodiments, the XY pluripotent and/or totipotent cells (i.e., XY ES cell or XY iPS cell) is maintained in an in vitro e in a media as described in WO201 1/156723, herein incorporated by reference in its entirety.

In one embodiment, the base medium is a low-salt DMEM. In a specific embodiment, the low-salt DMEM has a NaCl concentration of 85-130 mM. In one embodiment, the base medium is a low lity DMEM. In a specific embodiment, the low osmolality DMEM has an osmolality of 250-310 mOsm/kg. In one embodiment, the base medium is a low conductivity DMEM. In a specific embodiment, the low conductivity DMEM has a conductivity of 11 -13 mS/cm.

In other embodiments, the base medium exhibits an osmolality of no more than about 320, 310, 300, 290, 280, 275, 270, 260, 250, or 240 mOsm/kg. In one embodiment, the base medium or the medium comprising the base medium and the supplements ts an osmolality of no more than about 240-320, 250-310, 275-295, or 260-300 mOsm/kg. In a specific embodiment, the base medium or the medium comprising the base medium and the supplements exhibits an osmolality of about 270 mOsm/kg.

In other embodiments, the base medium ts a conductivity of no more than about 10.0, 10.5, 1 1.0, 1 1.5, 12.0, 12.5, 13.0, 13.5, or 14.0 mS/cm. In one embodiment, the base medium exhibits a conductivity of no more than about 10-14 mS/cm or 1 1 -13 mS/cm.

In a specific embodiment, the base medium exhibits a conductivity of about 12-13 mS/cm.

In a specific embodiment, the base medium exhibits a conductivity of about 12-13 mS/cm and an osmolality of about 260-300 mOsm/kg. In a further specific embodiment, the base medium comprises sodium chloride at a concentration of about 90 mM NaCl. In a further specific embodiment, the concentration of sodium chloride is about 70-95 mM. In a further ic embodiment, the base medium comprises sodium bicarbonate at a tration of less than about 35 mM. In a further specific embodiment, the concentration of sodium onate is about 20-30 mM.

In one embodiment, the base medium exhibits a concentration of a salt of an alkaline metal and a halide of no more than about 100 mM. In one embodiment, the salt of the alkaline metal and the halide is NaCl. In one embodiment, the concentration of the salt of the alkaline metal and halide is no higher than 90, 80, 70, 60, or 50 mM. In one embodiment, the concentration in the base medium of the salt of the alkaline metal and halide is about 60- 105, 70-95, or 80-90 mM. In a specific embodiment, the concentration is about 85 mM.

In one embodiment, the base medium exhibits a tration of a salt of ic acid. In one embodiment, the salt of carbonic acid is a sodium salt. In one embodiment, the sodium salt is sodium bicarbonate. In one embodiment, the concentration of carbonic acid salt in the base medium is no higher than 40, 35, 30, 25, or 20 mM. In one embodiment the concentration of carbonic acid salt in the base medium is about 10-40, in another ment about 20-30 mM. In a specific embodiment, the concentration is about 25 or 26 mM. In still other embodiments, the sodium bicarbonate concentration is about 26 mM, about 18 mM, about 18 mM to about 26 mM or about 18 mM to about 44 mM.

In one embodiment, the sum of the concentration of the salt of the ne metal and halide and the salt of carbonic acid in the base medium is no more than 140, 130, 120, 110, 100, 90, or 80 mM. In one embodiment, the sum of the concentration of the salt of the alkaline metal and halide and the salt of carbonic acid in the base medium is about 80-140, 85-130, 90-120, 95-120, or 100-120 mM. In a specific embodiment, the sum of the concentration of the salt of the alkaline metal and halide and the salt of carbonic acid in the base medium is about 115 mM.

In one embodiment, the molar ratio of the salt of the alkaline metal and halide and the salt of carbonic acid is higher than 2.5. In one embodiment, the ratio is about 2.6-4.0, 2.8- 3.8, 3-3.6, or 3.2-3.4. In one embodiment, the ratio is 3.3-3.5. In a specific embodiment, the ratio is 3.4.

In one embodiment, the base medium exhibits an osmolality of about 250-310 mOsm/kg, and a concentration of a salt of an alkaline metal and a halide of about 60-105 mM. In a further embodiment, the base medium has a concentration of a salt of ic acid of about 20-30 mM. In a further ment, the sum of the concentrations of the salt of an ne metal and halide and the salt of carbonic acid is about 80-140 mM. In a further embodiment, the conductivity of the base medium is about 12-13 mS/cm.

In one embodiment, the base medium comprises about 50 i 5 mM NaCl and about 26 i 5 mM carbonate, with an osmolality of about 218 i 22 mOsm/kg. In a specific embodiment, the base medium comprises about 3 mg/mL NaCl and 2.2 mg/mL sodium bicarbonate, with an osmolality of about 218 g.

In another ment, the base medium comprises about 87 i 5 mM NaCl and about 18 i 5 mM, with an osmolality of about 261 i 26 mOsm/kg. In a specific embodiment, the base medium comprises about 5.1 mg/mL NaCl and about 1.5 mg/mL sodium bicarbonate, with an osmolality of about 261 mOsm/kg.

In another embodiment, the base medium comprises about 110 i 5 mM NaCl and about 18 i 5 mM carbonate, with an osmolality of about 294 i 29 mOsm/kg. In a specific embodiment, the base medium comprises about 6.4 mg/mL NaCl and about 1.5 mg/mL sodium bicarbonate, with an osmolality of about 294 mOsm/kg.

In another embodiment, the base medium ts about 87 i 5 mM NaCl and about 26 i 5 mM carbonate, with an lity of about 270 i 27 mOsm/kg. In a specific embodiment, the base medium exhibits about 5.1 mg/mL NaCl and about 2.2 mg/mL sodium bicarbonate, with an osmolality of about 270 mOsm/kg.

In another embodiment, the base medium comprises about 87 i 5 mM NaCl, about 26 i 5 mM ate, and about 86 i 5 mM e, with an osmolality of about 322 i 32 mOsm/kg. In a specific embodiment, the base medium comprises about 5.1 mg/mL NaCl, about 2.2 mg/mL sodium bicarbonate, and about 15.5 mg/mL glucose, with an osmolality of about 322 mOsm/kg.

Additional base media that can be employed in the various methods and compositions disclosed herein e, a base medium comprising 50 i 5 mM NaCl and 26 i mM carbonate, with an osmolality of 218 i 22 mOsm/kg. In a particular embodiment, the base medium comprises about 3 mg/mL NaCl and 2.2 mg/mL sodium bicarbonate, with an osmolality of about 218 mOsm/kg.

In other ments, the base medium comprises 50 i 5 mM NaCl and 26 i 5 mM carbonate, with an osmolality of 218 i 22 mOsm/kg. In a specific embodiment, the base medium comprises about 3 mg/mL NaCl and 2.2 mg/mL sodium bicarbonate, with an osmolality of about 218 mOsm/kg.

In other embodiments, high glucose DMEM media (LifeTech) with NaHC03 concentrations as disclosed herein, including, about 44mM, 26mM or 18mM, were supplemented with 0.1mM nonessential amino acids, 1mM sodium pyruvate, 0.1mM 2- mercaptoethanol, 2mM L-glutamine, l each penicillin and streptomycin (LifeTech), % FBS (Hyclone), and 2000U/ml LIF pore).

C. Methodfor Making Targeted Genetic Modifications Various methods for making targeted c modifications that se the level and/or the activity of the Sry protein can be used. For example, in one ce, the targeted genetic modification employs a system that will generate a targeted genetic modification via a homologous recombination event. In other ces, the animal cell can be modified using nuclease agents that generate a single or double strand break at a targeted genomic location.

The single or double-strand break is then repaired by the non-homologous end g pathway (NHEJ). Such systems find use, for example, in generating targeted loss of function genetic modifications. Non-limiting methods for generating such targeted genetic modification are discussed in detail elsewhere herein, including, for example, the use of ing plasmids, small targeting vectors (smallTVECs) or large targeting vectors. See, also, Wang et al. (2013) Cell 0-918, Mandalos et al. (2012) PLOS ONE 7:e45768:1-9, and Wang et al. (2013) Nat Biotechnol. 31:530-532, each of which is herein incorporated by reference.

It is recognized that in specific embodiments, the targeted c modification of the Sry gene and/or the targeted genetic modification of any other polynucleotide of interest can occur while the pluripotent cell (i.e., ES cell) is being maintained in the culture media described herein (e.g. a medium that promotes the development of XY F0 fertile s).

Alternatively, the targeted genetic modification of the Sry gene and/or any other polynucleotide of interest can occur while the pluripotent cell (i.e., ES cell) is being maintained in different culture media, and subsequently transferred to the culture media disclosed herein (e. g. a medium that promotes the pment of XY F0 fertile females).

D. Method of Culturing and Maintaining a Pluripotent and/0r T0tip0tent Cell In A method for maintaining or ing an XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in an in vitro culture is provided, wherein the cell comprises a modification that decreases the level and/or activity of an Sry n and the cell is maintained in an in vitro culture under conditions described herein. Such methods of ining or culturing an XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in an in vitro culture is such as to e an increase in the number XY F0 fertile female animals upon the introduction of the non-human animal XY ES cells into a host embryo and following gestation of the host embryos.

While any media disclosed herein can be employed for such ining or culturing methods, one non-limiting example, includes culturing in a medium sing a base medium and supplements suitable for maintaining or culturing the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in culture, wherein the base medium or the medium sing the base medium and the supplements exhibits an osmolality from about 200 g to less than about 329 mOsm/kg.

In some embodiments, the base medium or the medium comprising the base medium and the supplements exhibits one or more of the following characteristic: a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50mM to about 110 mM; a carbonic acid salt tration of about l7mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt tration of about 85mM to about 130 mM; and/or a combination of any two or more thereof.

In one embodiment, the method comprises maintaining or culturing the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in a suitable culture medium that comprises a base medium and supplements, wherein the base medium or the medium comprising the base medium and the supplements comprises an osmolality of about 240-320 mOsm/kg, a conductivity of about 10-14 mS/cm, an alkaline metal halide salt concentration of about 50-105 mM, a salt of carbonic acid concentration of 10-40 mM, and/or a combined alkaline metal salt and carbonic acid salt tration of about 80-140 mM. In one embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in the medium (with supplements for maintaining ES cells) for a period of l, 2, 3, 4, 5, 6, 7, 8, 9, 10, ll, 12, or 13 days, or 2 weeks, 3 weeks, or 4 weeks prior to introduction into a host embryo. In a specific embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in the medium (low-salt base medium with ments for ining ES cells) for about 2-4 weeks prior to introduction into the host embryo.

In another embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in a medium with a low-salt base medium for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 days, 2 weeks, 3 weeks, or 4 weeks prior to introducing the donor cell into a host embryo. In a ic embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in a medium with a low-salt base medium at least 2-4 weeks prior to introduction of the cell into the host embryo.

In another embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is ined (e. g., frozen) in a medium that promotes XY fertile F0 females and the donor cell is thawed in and maintained in the medium that promotes XY fertile F0 females for at least 1, 2, 3, or 4 or more days before introducing the XY otent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) into the host embryo. In a specific embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an KY iPS cell) is passaged at least once in a medium that promotes XY fertile F0 females, the cell is frozen in the medium that promotes XY fertile F0 females, and the cell is thawed in a medium that promotes XY fertile F0 females and grown for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 days, 2 weeks, 3 weeks, 4 weeks, or more prior to introduction into the host .

In still another embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in the medium that promotes XY fertile F0 females for a period of one, two, three, or four days prior to introduction into a host embryo. In one embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained in the medium that promotes XY fertile F0 females for a period of 3 days.

In one embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is maintained the medium that promotes XY e F0 females before introduction into the host embryo for about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 days, 2 weeks, 3 weeks, or 4 weeks or more. In a specific embodiment, the donor cell is maintained in the medium that promotes XY fertile F0 females for at least a week before introduction into the host embryo. In a specific embodiment, the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is ined in the medium that promotes XY fertile F0 females for 2-4 weeks before introduction into the host embryo.

Thus, a method for maintaining or culturing an XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in culture is provided, wherein the cell is maintained under conditions that promote or favor development of a female XY animal following uction of the XY cell into a host embryo and following ion in a suitable female host.

In one aspect, a method for ining or culturing a donor XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) in culture is provided, under conditions as described herein, n ing introduction of the donor XY ES cell into a host embryo to form a F0 embryo and gestation of the F0 embryo in a suitable , the F0 embryo develops into an F0 animal that is at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or greater KY and is a female which, upon attaining sexual maturity, is fertile.

E. Generating F0 Embryos and F1 Progeny Having A Targeted Genetic Modification The various methods and compositions employing the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) having a decreased level and/or ty of Sry protein provided herein can be used to generate a genetically ed animal. s methods for introducing genetic modifications are discussed in detail elsewhere herein. i. Methodfor Making a Fertile Female XYNon-Human Animal in an F0 Generation A method for making a e female XY non-human animal in an F0 generation is provided. Such s se: (a) maintaining or culturing a donor non-human animal XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) having a modification that decreases the level and/or activity of an Sry n in a medium that promotes the development of XY fertile female ES cells; (b) ucing the donor XY non- human animal XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) into a host embryo; (c) gestating the host embryo; and, (d) obtaining an F0 XY female non- human animal, wherein upon attaining sexual maturity the F0 XY female non-human animal is fertile. In specific embodiments, the donor non-human animal XY donor cell can se at least one additional targeted genetic modification in a polynucleotide of interest. Such modifications are discussed in detail elsewhere herein.

The XY ES cells having a modification that decreases the level and/or activity of an Sry protein can be ined without a lt medium and can develop into an XY fertile female.

In some embodiments, the medium that promotes the development of XY fertile F0 female s can comprise a low-salt based medium which comprises a base medium and supplements suitable for maintaining or culturing the non-human mammalian ES cell in culture, wherein the low-salt base medium exhibits a characteristic comprising one or more of the following: an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg; a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50 mM to about 110 mM; a carbonic acid salt concentration of about 17 mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt concentration of about 85 mM to about 130 mM; and/or a combination of any two or more thereof.

In other embodiments, such methods for making a fertile female XY non-human animal in an F0 tion can be performed using the mediums disclosed herein including, but not limited to, (a) a base medium comprising 50 i 5 mM NaCl, 26 i 5 mM carbonate, and 218 i 22 mOsm/kg; (b) a base medium comprising about 3 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 218 mOsm/kg; (c) a base medium comprising 87 i 5 mM NaCl, 18 i 5 mM carbonate, and 261 i 26 mOsm/kg; (d) a base medium comprising about 5.1 mg/mL WO 00805 NaCl, 1.5 mg/mL sodium bicarbonate, and 261 mOsm/k; (e) a base medium comprises 110 i mM NaCl, 18 i 5 mM carbonate, and 294 i 29 mOsm/kg; (f) a base medium comprises about 6.4 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 294 mOsm/kg; (g) a base medium ses 87 i 5 mM NaCl, 26 i 5 mM carbonate, and 270 i 27 mOsm/kg; (h) a base medium comprises about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 270 mOsm/kg; (i) a base medium comprises 87 i 5 mM NaCl, 26 i 5 mM carbonate, 86 i 5 mM glucose, and 322 i 32 mOsm/kg; and/or (1') a base medium comprises about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, 15.5 mg/mL glucose, and 322 mOsm/kg.

The genetically modified XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) having a modification that ses the level and/or activity of an Sry protein and having been ed in the medium that promotes the development of XY F0 fertile females can be implanted into a host embryo. Cells that have been ted into a host embryo are referred to herein as “donor cells.” In specific embodiments, the genetically modified XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) is from the same strain as the host embryo or from a different strain as the host embryo. se, the surrogate mother can be from the same strain as the genetically modified XY pluripotent and/or tent cell (i.e., an XY ES cell or an XY iPS cell) and/or the host embryo, or the surrogate mother can be from a different strain as the genetically modified XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) and/or the host embryo. In one embodiment, the XY donor cell is implanted into an XX host embryo.

A variety of host embryos can be employed in the methods and compositions sed herein. In some embodiments, the XY pluripotent and/or totipotent cells (i.e., the XY ES cell or the XY iPS cell) having the targeted genetic modification resulting in a decreased level and/or activity of the Sry n are introduced into a pre-morula stage embryo from a corresponding organism, e. g., an 8-cell stage embryo. See, e.g., US 259, US 7,659,442, US 7,294,754, and US 2008-0078000 A1, all of which are incorporated by reference herein in their entireties. In other embodiments, the donor ES cells may be implanted into a host embryo at the 2-cell stage, 4-cell stage, 8-cell stage, 16-cell stage, 32-cell stage, or 64-cell stage host embryo. In another embodiment, the host embryo is a blastocyst. In one embodiment, the host embryo is in a stage selected from a astocyst embryo, a pre-morula stage, a morula stage, an uncompacted morula stage, and a compacted morula stage. In one embodiment, when employing a mouse embryo, the host embryo stage is selected from a Theiler Stage 1 (TSl), a TS2, a TS3, a TS4, a TS5, and a TS6, , with nce to the Theiler stages described in Theiler (1989) "The House Mouse: Atlas of Mouse Development," er-Verlag, New York. In a specific embodiment, the Theiler Stage is selected from TSl, TS2, TS3, and a TS4. In one embodiment, the host embryo comprises a zona pellucida, and the donor cell is an XY ES cell that is introduced into the host embryo h a hole in the zona pellucida, while in other embodiments, the host embryo is a zona-less embryo. In yet other specific embodiments, the morula-stage host embryo is aggregated.

Nuclear transfer techniques can also be used to generate the genetically modified animals. Brieﬂy, methods for nuclear transfer include the steps of: (l) enucleating an oocyte; (2) isolating a donor cell or nucleus to be combined with the enucleated oocyte; (3) inserting the cell or nucleus into the enucleated oocyte to form a reconstituted cell; (4) implanting the reconstituted cell into the womb of an animal to form an embryo; and (5) allowing the embryo to develop. In such methods oocytes are generally retrieved from deceased animals, although they may be isolated also from either oviducts and/or ovaries of live animals.

Oocytes can be d in a variety of medium known to those of ordinary skill in the art prior to enucleation. ation of the oocyte can be performed in a number of s well known to those of ordinary skill in the art. Insertion of the donor cell or s into the enucleated oocyte to form a reconstituted cell is usually by microinjection of a donor cell under the zona pellucida prior to fusion. Fusion may be d by application of a DC electrical pulse across the contact/fusion plane rofusion), by exposure of the cells to fusion-promoting chemicals, such as polyethylene , or by way of an inactivated virus, such as the Sendai virus. A reconstituted cell is typically activated by electrical and/or non- electrical means , during, and/or after fusion of the nuclear donor and recipient .

Activation methods include electric pulses, chemically induced shock, penetration by sperm, increasing levels of divalent cations in the oocyte, and reducing phosphorylation of cellular proteins (as by way of kinase inhibitors) in the oocyte. The activated reconstituted cells, or s, are typically cultured in medium well known to those of ordinary skill in the art and then transferred to the womb of an animal. See, for example, US20080092249, WO/l999/005266A2, US20040177390, WO/2008/017234Al, and US Patent No. 7,612,250, each of which is herein incorporated by reference.

The host embryo comprising the cally modified XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell) having the decreased level and/or activity of the Sry protein is incubated until the cyst stage and then implanted into a surrogate mother to produce an F0 animal. Animals bearing the genetically modified genomic locus can be identified via modification of allele (MOA) assay as described herein.

In one embodiment, the host embryo comprising the genetically modified XY pluripotent and/or totipotent cells (i.e., an XY ES cell or an XY iPS cell) having the sed level and/or activity of the Sry n is maintained in a medium that promotes the development of XY e female ES cells (i.e., a low-salt base medium) for one, two, three, or four or more days prior to implantation in a suitable host. Such methods provide for favoring the generation of an F0 fertile female animal.

] In one embodiment, the cultured host embryo is implanted into a surrogate mother, and the cultured host embryo is gestated in the surrogate .

In specific embodiments, upon introduction of the non-human animal XY pluripotent and/or totipotent cells (i.e., an XY ES cell or an XY iPS cell) into a host embryo and following ion of the host embryo, at least 15%, 20%, 30%, 40%, 50%, 60%, 70%, 75%, 80% 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% of the F0 non-human animals are XY s which upon attaining sexual maturity the F0 XY female non-human mammal is fertile.

] Further provided is an F0 embryo comprising an inner cell mass having at least one heterologous stem cell comprising an XY ES cell or XY iPS cell having a targeted genetic modification that decreases the level and/or activity of the Sry protein.

] The various methods described herein to generate a fertile female XY non-human animal in an F0 generation can employ XY pluripotent and/or totipotent cells (i.e., an XY ES cell or an XY iPS cell) having (1) the genetic modification to reduce the level and/or activity of the Sry polypeptide; and, in specific embodiments, (2) one or more additional targeted genetic modification in a polynucleotide of interest. As outlined elsewhere herein, at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more additional targeted c modifications can be made in the XY pluripotent and/or totipotent cell (i.e., an XY ES cell or an XY iPS cell). In such instances, the F0 fertile female XY non-human animal can comprises one or more of these additional ed genetic modifications.

In other embodiments, the F0 fertile female XY non-human animal produces l, 2, 3, 4, 5, 6, 7, 8, or 9 litters during its me. In one embodiment, the F0 fertile female XY non-human animal produces at least 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 offspring per litter. In one embodiment, the F0 fertile female XY non-human animal produces about 4-6 offspring per litter. In one embodiment, the F0 e female XY non-human animal produces 2-6 litters, wherein each litter has at least 2, 3, 4, 5, or 6 offspring. In one embodiment, at least about %, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 60%, 70%, 80%, 85%, 90%, 95% or 100% of the offspring are XY fertile female offspring.

A method for generating a rodent litter (i.e., a mouse or a rat ) is also provided and comprises introducing an XY pluripotent and/or totipotent donor cell (i.e., an XY donor ES cell or XY donor iPS cell) having the decreased level and/or activity of Sry protein prepared according to the methods set forth herein into host embryos, gestating the embryos in a suitable segregate , and obtaining F0 progeny that comprises at least one XY female rodent that upon reaching sexual maturity is a fertile XY female rodent. In one embodiment, the percentage of F0 XY female s born that upon reaching sexual maturity are fertile is about 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 60%, 70%, 75%, 80%, 85%, 95% or 100%.

In other embodiments, the F0 progeny ed from such methods are about 3%, about 10% or more, or about 63% or more derived from the genetically modified donor XY cell.

The methods and compositions provided herein allow for at least 1%, 3%, 5%, %, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75% or greater of the F0 animals to have the targeted genetic modification (i.e., the se in Sry protein level and/or activity and/or the targeted genetic modification to a cleotide of interest) to transmit the genetic modification to the F1 progeny.

In one embodiment, the F0 generation female XY non-human animal and/or the male XY non-human animal is at least 90%, 92%, 94%, 96%, 98%, 99%, or 99.8% derived from the donor cell. In one embodiment, the F0 female XY non-human animal and/or the F0 male XY non-human animal has a coat color that is 100% derived from the donor cell.

In one embodiment, the non-human female XY animal in the F0 generation is a rodent (i.e., a mouse or a rat) and has a coat color 100% derived from the donor cell. In one embodiment, the non-human female XY non-human animal formed in the F0 tion is at least 90%, 92%, 94%, 96%, 98%, or 99.8% derived from the XY donor cell. In one embodiment, the non-human female XY animal in the F0 tion is about 100% derived from the donor cell. In one embodiment, the contribution of a host embryo cell to the non- human female XY animal in the F0 generation is ined by a quantitative assay that is capable of detecting 1 cell in 2,000 (0.05%), and no tissue of the female XY animal is positive for host embryo cell contribution. ii. Various Methods ding the Female Fertile XY F0 Generation In specific embodiments, the resulting female fertile XY F0 generation derived from the XY pluripotent and/or totipotent cells (i.e., the XY ES cell or XY iPS cell) having 2015/038001 the genetic modification that decreases the level and/or activity of the Sry protein is crossed to an animal to obtain F1 generation ing. In ic embodiments, the female fertile XY F0 is crossed to a wild type animal. In one embodiment, the female XY F0 non-human mammal is fertile when crossed to a wild type mouse. In specific embodiments, the wild type mouse is C57BL/6. The F1 progeny can be genotyped using ic primers and/or probes to determine if the targeted genetic modification comprising the decreased level and/or activity of the Sry protein is present. Moreover, if additional targeted genetic modifications were present in the F0 generation, the F1 progeny can be genotyped using specific primers and/or probes that determine if such modifications are t. An riate Fl progeny for a desired use can then be identified. In specific embodiments, Fl y g the genetic modification that reduced the level and/or activity of the Sry protein are selected. In other embodiments, Fl progeny lacking the genetic modification that reduced the level and/or activity of the Sry protein and which comprise at least one additional targeted c modification are selected.

In one non-limiting example, following genotyping with ic primers and/or probes, Fl animals that are heterozygous for the targeted genetic modification to the polynucleotide of interest and lacking the targeted modification that reduces the level and/or activity of the Sry protein are crossed to one another. Such a cross produces an F2 progeny that is homozygous for the genetically ed genomic locus of interest and does not comprise the genetic modification to reduce Sry protein levels and/or activity.

Further provided is a method of producing a transgenic non-human animal homozygous for a targeted genetic modification in the F1 generation. The method ses (a) crossing an F0 XY fertile female non-human animal having a targeted genetic modification that decreases the level and/or activity of the Sry protein with a F0 XY male non-human animal, wherein the F0 XY fertile female non-human animal and the F0 XY male non-human animal are each heterozygous for the same genetic modification of a polynucleotide of interest, and (b) ing an F1 progeny that is homozygous for the targeted genetic modification in the polynucleotide of interest. In a specific embodiment, the F1 progeny selected are homozygous for the targeted genetic cation in the polynucleotide of interest and lack the targeted genetic modification that decreases the activity and/or level of the Sry protein. Such methods can be employed to develop breeding pairs of non-human animals, each fully d from a donor ES cell or iPS cell, in the same F0 generation.

Various methods can be employed to obtain the F0 animals described above. In one non-limiting embodiment, an XY cell clone with a targeted modification in a polynucleotide of interest on any chromosome is isolated. It is ized that various methods can be used to generate the targeted modification in the polynucleotide of st.

In a second step, a targeted modification is introduced into the Sry gene such that the modification decreases the level and/or activity of the Sry protein. Such methods will further employ culturing the XY ES cell in a media that es the development of XY F0 fertile females, as describe in detail elsewhere . Methods of targeted modification of the Sry gene are disclosed in detail elsewhere herein and can comprise, for example, the use of a targeting vector (including an LTVEC) either alone or in ation with a nuclease as described elsewhere herein (i.e., a Talen or CRISPR- or ZFN- system). A subclone is isolated that comprises both the first ed modification in the polynucleotide of interest and the second targeted modification of the Sry gene that decreases the level and/or activity of the Sry protein. Both the original XY clone with the targeted modification in the polynucleotide of interest and the XY subclone comprising both the targeted modification to the Sry gene and the polynucleotide of interest are introduced into separate non-human host embryos, as discussed elsewhere herein. In specific embodiments, the non-human host embryos comprise a pre-morula embryo (i.e., an 8 cell stage embryo). Each of the non- human host embryos comprising the modified pluripotent cells is uced into a surrogate mother for gestation. Each of the surrogate mothers es F0 progeny comprising the targeted genome modification (i.e., an F0 XY male having the targeted modification in the polynucleotide of interest and an F0 XY fertile female having the targeted modification in the polynucleotide of interest and having the genetic modification that decreases the level and/or activity of the Sry n). In specific embodiments, each of the targeted genomic modifications is capable of being transmitted through the germline. Each of these F0 animals are bred to one another, to generate an F1 animal sing a homozygous targeted cation in the polynucleotide of interest. One-quarter of the F1 generation are expected to be homozygous for the targeted modification in the polynucleotide of interest. Fl progeny can be ed to retain the ed modification to the Sry gene or the F1 progeny can be ed to not retain the targeted modification to the Sry gene.

In another embodiment, the uction of the targeted modification of the Sry gene employing a targeting vector (and, in specific embodiments, nucleases such as Talen, Crispr, or an) can occur simultaneously with the vector targeting for the genetic modification of the polynucleotide of interest. Such methods allow for the generation of an XY ES cell having both a genetic modification that decreases the level and/or activity of the Sry protein and further comprises the targeted modification to the polynucleotide of interest.

In one ment, the F1 generation progeny comprises a genome completely derived from the donor ES cell. In other ments, the frequency of s of F0 generation male and F0 generation female mice that give rise to fully ES cell-derived mice is 100%.

II. Methods and Compositionsfor Modifying a Challenging Target Genomic Locus or a Target Genomic Locus on the Y Chromosome Methods and itions are provided that allow for modifying a target genomic locus on the Y some in a cell. Further provided are s that allow for modifying a “challenging” genomic locus. The term “challenging locus” includes a somal region that is difficult to target by conventional gene targeting strategies. Such loci can be located on the Y chromosome, the X chromosome, or an autosome. In certain embodiments, challenging loci are located within or in proximity to gene-poor, repeat-rich, and/or largely heterochromatic chromosomal regions. See, e. g., Bernardini et al., Proc. Natl. Acad. Sci.

USA 111:7600-7605 (2014), herein incorporated by reference in its entirety for all purposes.

In certain embodiments, a challenging locus is located within or in proximity to chromosomal regions in which accessibility of the chromosomal DNA is limited by chromatin structure. In certain embodiments, a challenging locus is within or in proximity to chromosomal regions characterized by a high tage of heterochromatin, such as at least about ~20%, at least about ~30%, at least about 40%, at least about 50%, at least about 60%, or at least about 70% heterochromatin. In certain embodiments, a challenging locus is located within or in ity to chromosomal regions that have undergone duplications and rearrangements or that are characterized by the presence of repeats or ed repeats. See, e. g., Gubbay et al., Proc. Natl. Acad. Sci. USA 3-7957 (1992), herein incorporated by reference in its entirety for all purposes.

The term “chromatin” includes nucleoprotein complexes which t and organize cellular genetic material to contain it within cells. The term “heterochromatin” includes s in the genome that are in a highly condensed state and are generally transcriptionally silent. Heterochromatin is generally more tightly coiled and generally has more repetitive DNA sequences than euchromatin. The term “euchromatin” includes regions in the genome characterized by more extended and less condensed chromatin domains that are often transcriptionally active and accessible.

The term “exposing” includes using any method by which desired components are brought into immediate proximity or direct contact.

Methods and compositions are provided that allow for modifying a challenging target genomic locus or a target genomic locus on the Y chromosome in a cell. Perhaps due to unique structural es of the Y chromosome, conventional gene targeting strategies in mouse embryonic stem cells to generate mutations on the Y-linked genes has had limited success. Therefore, often the understanding of the functions of murine Y-linked genes is limited to insights gained from studies of mice that carry spontaneous deletions, random gene trap insertions or autosomal transgenes. Methods provided herein allow for the targeting of a genomic locus on the Y some by employing a targeting vector in the absence of or in combination with a nuclease agent.

Some such s utilize a small ing vector or VEC. A “smallTVEC” includes a targeting vector that comprises short homology arms. The length of a homology arm on a smallTVEC can be from about 400-1000 bp. A homology arm of the smallTVEC can be of any length that is sufficient to promote a gous recombination event with a corresponding target site, including for example, from about 400 bp to about 500 bp, from about 500 bp to about 600 bp, from about 600 bp to about 700 bp, from about 700 bp to about 800 bp, from about 800 bp to about 900 bp, or from about 900 bp to about 1000 bp. A red length of a homology arm on a VEC is from about 700 bp to about 800 bp. In another embodiment, the sum total of 5’ and 3’ homology arms of the smallTVEC is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb. In such methods, the short length of the gy arms increases the targeting efficiency as compared to a targeting vector with longer homology arms. Due to the nature of the Y chromosome which has highly repetitive sequences, the short arms of the smallTVECs allow for highly specific targeting on the Y some.

] Methods are provided for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell comprising a target c locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) introducing into the cell a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm corresponding to a first and a second target site; and (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus on the Y chromosome. In specific embodiments, the sum total of the first homology arm and the second homology arm of the targeting vector is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb or at least 10 kb and less than 150 kb. In some embodiments, a smallTVEC is employed. In specific embodiments, an LTVEC is employed. Similar methods can be med when targeting a challenging target genomic locus. In one non-limiting embodiment, such methods are performed employing the culture media that promotes the development of XY F0 fertile females sed herein and thereby generating XY F0 fertile female animals. In other instance, the s described herein are ed to produce a targeted genetic modification in the Sry gene, as discussed elsewhere herein.

Further provided are methods for modifying a target genomic locus on the Y chromosome in a cell sing: (a) providing a cell comprising a target c locus on the Y some comprising a recognition site for a nuclease agent, (b) introducing into the cell (i) the nuclease agent, wherein the se agent s a nick or double-strand break at the first recognition site; and, (ii) a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm corresponding to a first and a second target site located in ient proximity to the first recognition site; and (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus on the Y chromosome. In specific embodiments, the sum total of the first homology arm and the second homology arm of the targeting vector is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb or at least 10 kb and less than 150 kb. In some embodiments, a smallTVEC is employed. In specific embodiments, an LTVEC is employed. Similar methods can be performed when targeting a challenging target genomic locus. In one non-limiting embodiment, such methods are performed employing the e media that promotes the development of XY F0 fertile females sed herein and thereby generating XY F0 fertile female animals. In other instance, the methods described herein are employed to produce a targeted genetic modification in the Sry gene, as discussed elsewhere herein.

It is recognized that the various methods disclosed herein to te a targeted cation in a genomic locus of the Y chromosome (or any challenging genomic locus) 2015/038001 employing a targeting vector, a smallTVEC, or an LTVEC can be performed in any cell type, and is not limited to an XY pluripotent and/or totipotent cell. Such cell types include, but are not limited to, a human cell, a non-human cell, a mammalian cell, non-human mammalian cell, a rodent cell, a mouse cell, a rat cell, a hamster cell, a fibroblast cell or any other host cell. Such cells include pluripotent cells, including, for example, induced pluripotent stem (iPS) cells, mouse embryonic stem (ES) cells, rat nic stem (ES) cells, human embryonic (ES) cells, or developmentally restricted human progenitor cells.

Methods are further disclosed to generate a large deletion on the Y chromosome employing any of the various nuclease agents provided herein (e. g., CRISPR gRNAs in ation with Cas9; ZFNs; or TALENs). Such a deletion on the Y chromosome can be a on of an endogenous c acid sequence. The deletion can range from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 600 kb, from about 600 kb to about 700 kb, from about 700 kb to about 800 kb, from about 800 kb to about 900 kb, from about 900 kb to about 1 Mb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb. In one embodiment, the deletion is greater than 500 kb. In another embodiment, the deletion is from about 500 kb to about 600 kb. In a specific embodiment, the deletion is about 500 kb. Such a deletion on the Y some can be a deletion of any nucleic acid sequence. In one embodiment, the deletion comprises a gene that is ated with ity/infertility. The deletion on the Y chromosome can comprise a deletion of multiple genes. In such methods, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more genes can be deleted. In specific embodiments, the Kdm5d gene (Lysine (K)- specific demethylase 5d; for example, Entrez Gene ID 20592 (mus musculus)) and/or the Usp9y gene (ubiquitin specific peptidase 9, y-linked; for example, Entrez Gene ID 107868(mus musculus)) is targeted for deletion. In other embodiments, the Sry gene is ed for deletion.

A. Nuclease Agents and Recognition Sites for Nuclease Agents The term “recognition site for a nuclease agent” includes a DNA sequence at which a nick or double-strand break is induced by a nuclease agent. The recognition site for a nuclease agent can be endogenous (or native) to the cell or the ition site can be exogenous to the cell. In specific ments, the recognition site is exogenous to the cell and thereby is not naturally occurring in the genome of the cell. In still further embodiments, the recognition site is exogenous to the cell and to the polynucleotides of st that one desires to be positioned at the target locus. In further embodiments, the exogenous or endogenous ition site is present only once in the genome of the host cell. In ic embodiments, an endogenous or native site that occurs only once within the genome is identified. Such a site can then be used to design nuclease agents that will produce a nick or double-strand break at the endogenous recognition site.

The length of the recognition site can vary, and includes, for example, recognition sites that are about 30-36 bp for a zinc finger nuclease (ZFN) pair (i.e., about 15-18 bp for each ZFN), about 36 bp for a Transcription Activator-Like Effector Nuclease ), or about 20bp for a CRISPR/Cas9 guide RNA.

In one embodiment, each monomer of the nuclease agent recognizes a recognition site of at least 9 nucleotides. In other embodiments, the recognition site is from about 9 to about 12 nucleotides in length, from about 12 to about 15 nucleotides in length, from about to about 18 nucleotides in length, or from about 18 to about 21 nucleotides in , and any combination of such subranges (e. g., 9-18 nucleotides). It is recognized that a given nuclease agent can bind the recognition site and cleave that g site or alternatively, the nuclease agent can bind to a sequence that is different from the recognition site. Moreover, the term recognition site comprises both the nuclease agent g site and the nick/cleavage site irrespective whether the nick/cleavage site is within or outside the se agent binding site. In another variation, the cleavage by the se agent can occur at nucleotide positions immediately opposite each other to produce a blunt end cut or, in other cases, the incisions can be red to produce single-stranded overhangs, also called “sticky ends”, which can be either 5' overhangs, or 3' ngs.

Any nuclease agent that induces a nick or double-strand break into a desired recognition site can be used in the methods and compositions disclosed herein. A naturallyoccurring or native nuclease agent can be employed so long as the nuclease agent induces a nick or double-strand break in a desired recognition site. Alternatively, a modified or engineered nuclease agent can be employed. An “engineered nuclease agent” includes a nuclease that is engineered (modified or derived) from its native form to specifically recognize and induce a nick or double-strand break in the desired recognition site. Thus, an engineered nuclease agent can be d from a native, naturally-occurring nuclease agent or it can be artificially created or synthesized. The modification of the nuclease agent can be as little as one amino acid in a protein cleavage agent or one nucleotide in a nucleic acid cleavage agent. In some embodiments, the engineered nuclease induces a nick or double- strand break in a ition site, wherein the recognition site was not a sequence that would have been recognized by a native (non-engineered or non-modified) nuclease agent.

Producing a nick or double-strand break in a recognition site or other DNA can be referred to herein as “cutting” or “cleaving” the recognition site or other DNA.

Active variants and fragments of the exemplified recognition sites are also provided. Such active variants can comprise at least 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more ce identity to the given recognition site, wherein the active variants retain biological activity and hence are capable of being recognized and cleaved by a nuclease agent in a ce-specific manner. Assays to measure the double-strand break of a recognition site by a nuclease agent are known in the art (e. g., TaqMan® qPCR assay, Frendewey D. et (11., Methods in Enzymology, 2010, - 307, which is incorporated by reference herein in its entirety).

In specific ments, the recognition site is positioned within the polynucleotide encoding the selection marker. Such a position can be located within the coding region of the selection marker or within the tory regions, which inﬂuence the expression of the selection marker. Thus, a recognition site of the nuclease agent can be located in an intron of the selection marker, a promoter, an enhancer, a regulatory region, or any non-protein-coding region of the polynucleotide ng the selection marker. In specific embodiments, a nick or double-strand break at the recognition site disrupts the activity of the selection . Methods to assay for the presence or absence of a onal selection marker are known.

In one embodiment, the se agent is a ription Activator-Like Effector Nuclease (TALEN). TAL effector nucleases are a class of sequence-specific nucleases that can be used to make double-strand breaks at specific target sequences in the genome of a prokaryotic or eukaryotic organism. TAL effector nucleases are created by fusing a native or engineered transcription activator-like (TAL) effector, or onal part thereof, to the catalytic domain of an clease, such as, for example, Fold. The unique, modular TAL effector DNA binding domain allows for the design of proteins with potentially any given DNA recognition specificity. Thus, the DNA binding domains of the TAL effector nucleases can be engineered to recognize specific DNA target sites and thus, used to make double- strand breaks at desired target sequences. See, ; Morbitzer et a1. (2010) PNAS 10.1073/pnas.1013133107; Scholze & Boch (2010) nce 1:428-432; Christian et a1. Genetics (2010) 186:757-761; Li et a1. (2010) Nuc. Acids Res. (2010) 2015/038001 doi:10.1093/nar/gkq704; and Miller et a1. (2011) Nature Biotechnology 29:143—148; all of which are herein incorporated by reference. es of suitable TAL ses, and methods for ing suitable TAL nucleases, are disclosed, e. g., in US Patent Application No. 2011/0239315 A1, 2011/0269234 A1, 145940 A1, 2003/0232410 A1, 2005/0208489 A1, 2005/0026157 A1, 2005/0064474 A1, 2006/0188987 A1, and 2006/0063231 A1 (each hereby incorporated by reference). In various ments, TAL effector ses are engineered that cut in or near a target nucleic acid sequence in, e.g., a locus of interest or a genomic locus of interest, wherein the target nucleic acid sequence is at or near a sequence to be modified by a targeting vector. The TAL nucleases suitable for use with the various methods and compositions provided herein include those that are specifically designed to bind at or near target nucleic acid sequences to be modified by targeting vectors as bed herein.

In one embodiment, each monomer of the TALEN comprises 33-35 TAL repeats that recognize a single base pair via two hypervariable residues. In one embodiment, the nuclease agent is a chimeric protein comprising a TAL repeat-based DNA binding domain operably linked to an independent nuclease. In one embodiment, the independent nuclease is a FokI endonuclease. In one embodiment, the nuclease agent comprises a first TAL-repeat- based DNA binding domain and a second TAL-repeat-based DNA binding domain, wherein each of the first and the second TAL-repeat-based DNA binding domain is ly linked to a FokI nuclease, wherein the first and the second peat-based DNA binding domain ize two contiguous target DNA sequences in each strand of the target DNA sequence ted by a spacer sequence of g length (12-20 bp), and wherein the FokI nuclease subunits dimerize to create an active nuclease that makes a double strand break at a target sequence.

The nuclease agent employed in the various methods and compositions sed herein can further comprise a zinc-finger nuclease (ZFN). In one embodiment, each monomer of the ZFN comprises 3 or more zinc finger-based DNA binding domains, wherein each zinc -based DNA binding domain binds to a 3bp subsite. In other embodiments, the ZFN is a chimeric protein comprising a zinc finger-based DNA binding domain operably linked to an independent nuclease. In one embodiment, the independent endonuclease is a FokI endonuclease. In one embodiment, the nuclease agent comprises a first ZFN and a second ZFN, wherein each of the first ZFN and the second ZFN is operably linked to a FokI nuclease subunit, wherein the first and the second ZFN recognize two contiguous target DNA sequences in each strand of the target DNA sequence separated by about 5-7 bp spacer, and n the Fokl nuclease subunits dimerize to create an active nuclease to make a double strand break. See, for example, US20060246567; US20080182332; US20020081614; US20030021776; WO/2002/057308A2; US20130123484; US20100291048; WO/2011/017293A2; and Gaj et al. (2013) Trends in Biotechnology, 31(7):397-405 each of which is herein incorporated by reference.

In still another embodiment, the nuclease agent is a meganuclease.

Meganucleases have been classified into four families based on ved sequence motifs, the families are the ADG, GIY-YIG, H-N-H, and His-Cys box es. These motifs participate in the coordination of metal ions and hydrolysis of phosphodiester bonds.

Meganucleases are notable for their long recognition sites, and for tolerating some sequence polymorphisms in their DNA substrates. Meganuclease domains, structure and function are known, see for e, Guhan and Muniyappa (2003) Crit Rev Biochem Mol Biol 38: 199- 248; Lucas et al., (2001) Nucleic Acids Res 29:960-9; Jurica and Stoddard, (1999) Cell Mol Life Sci 55:1304-26; Stoddard, (2006) Q Rev Biophys 38:49-95; and Moure et al., (2002) Nat Struct Biol 9:764. In some examples a naturally occurring variant, and/or engineered derivative meganuclease is used. Methods for modifying the cs, cofactor interactions, expression, optimal conditions, and/or recognition site icity, and screening for activity are known, see for example, Epinat et al., (2003) Nucleic Acids Res 31:2952-62; ier et al., (2002) Mol Cell 10:895-905; Gimble et al., (2003) Mol Biol 334:993-1008; Seligman et al., (2002) Nucleic Acids Res 30:3870-9; Sussman et al., (2004) JMol Biol 342:31-41; Rosen et al., (2006) Nucleic Acids Res 34:4791-800; Chames et al., (2005) c Acids Res 33:el78; Smith et al., (2006) Nucleic Acids Res 34:el49; Gruen et al., (2002) Nucleic Acids Res 30:e29; Chen and Zhao, (2005) Nucleic Acids Res 33:el54; WO2005105989; WO2003078619; WO2006097854; 097853; WO2006097784; and WO2004031346.

Any clease can be used herein, including, but not limited to, I-Scel, I- SceII, I-SceIII, I—SceIV, I-SceV, I—SceVI, I-SceVII, I-Ceul, I-CeuAIIP, I—Crel, I-CrepsbIP, I- CrepsbIIP, I—CrepsbIIIP, I-CrepsbIVP, , I-Ppol, PI-Pspl, F-SceI, I, , F- TevI, F—TevII, I-Amal, I-Anil, I—Chul, I—Cmoel, I-Cpal, I-CpaII, I-Csml, I-Cvul, I-CvuAIP, I-Ddil, I-DdiII, I—DirI, I—Dmol, , I—HmuII, I-HsNIP, I-LlaI, , I-NaaI, I—NanI, I- NcIIP, I-NngP, I-NitI, I-NjaI, I—Nsp236IP, I-Pakl, I-PboIP, I-PcuIP, I-PcuAI, I-PcuVI, 1- PngP, I-PobIP, I-Porl, I-PorIIP, I-PprP, I-SpBetaIP, I—Scal, I-SexIP, I-SneIP, I-SpomI, I- , I-SpomIP, I-SpomlIP, I-SquIP, I-Ssp6803l, I-SthPhiJP, hiST3P, I- SthPhiSTe3bP, I-TdeIP, I-TevI, I-Tevll, I—TevIII, I-UarAP, I—UarHGPAIP, I-UarHGPAl3P, I-VinIP, I-ZbiIP, PI-Mtul, PI—MtuHIP PI—MtuHIIP, l, PI-PfuII, PI-Pkol, PI—Pkoll, PI- Rma43812IP, PI—SpBetaIP, I, PI-TfuI, PI-TfuII, PI-ThyI, PI-TliI, PI—TliII, or any active variants or fragments thereof.

In one embodiment, the meganuclease recognizes double-stranded DNA sequences of 12 to 40 base pairs. In one embodiment, the clease izes one perfectly matched target sequence in the genome. In one embodiment, the meganuclease is a homing se. In one ment, the homing nuclease is a LAGLIDADG family of homing nuclease. In one embodiment, the LAGLIDADG family of homing nuclease is selected from I-SceI, I-CreI, and I-Dmol.

Nuclease agents can further comprise restriction endonucleases, which include Type I, Type II, Type III, and Type IV endonucleases. Type I and Type III restriction endonucleases recognize specific recognition sites, but typically cleave at a variable position from the nuclease binding site, which can be hundreds of base pairs away from the cleavage site (recognition site). In Type II systems the restriction activity is independent of any methylase activity, and cleavage typically occurs at specific sites within or near to the binding site. Most Type II enzymes cut palindromic sequences, however Type IIa enzymes recognize non-palindromic ition sites and cleave outside of the recognition site, Type IIb enzymes cut sequences twice with both sites outside of the recognition site, and Type IIs enzymes recognize an asymmetric ition site and cleave on one side and at a d distance of about 1-20 nucleotides from the recognition site. Type IV restriction enzymes target methylated DNA. Restriction enzymes are further described and classified, for example in the REBASE database ge at rebase.neb.com; Roberts et al., (2003) Nucleic Acids Res 31 :418-20), s et al., (2003) Nucleic Acids Res 31 :1805-12, and Belfort et al., (2002) in Mobile DNA 11, pp. 761-783, Eds. Craigie et al., (ASM Press, gton, DC).

The nuclease agent employed in the various methods and compositions can also comprise a CRISPR/Cas system. Such systems can employ a Cass? nuclease, which in some instances, is cation—Optimized fer the desired cell type in which it is to he sed.

The system further s a fused chNA~trachNA construct that functions with the coden—optimized Cas9. This single RNA is Often referred to as a guide RNA or gRNA, Within a gRNA, the chNA perticn is identified as the ‘target sequence" for the given recognition site and the trachNA is often referred to as the ‘scaffold’. This system has been shown to functien in a variety of euliar‘yotic and prokaryetic cells, Briefly, a short DNA fragment containing the target sequence is inserted into a guide RNA expression plasmid.

The gRNA expression plasmid ccniprises the target sequence (in some einbcdinients around ’20 nuclentides), a foiin of the trachNA ce (the scaffold) as well as a suitable promoter that is active in the cell and ary elements for proper processing in enharyotic cells. Many of the systems rely on custom, complementary oligos that are annealed to form a double stranded DNA and then cloned into the gRNA expression plasmid. The gRNA sion cassette and the Case”) expression cassette are then introduced into the cell. See, for example, Mali P et al. (2013) Science 2013 Feb 15; 339 (6121):823-6; Jinek M et al. e 2012 Aug 17;337(6096):816-21; Hwang WY et al. Nat Biotechnol 2013 Mar;31(3):227-9; Jiang W et al. Nat Biotechnol 2013 Mar;31(3):233-9; and, Cong L et al.

Science 2013 Feb 15;339(6121):819-23, each of which is herein incorporated by reference.

The methods and compositions disclosed herein can utilize Clustered Regularly Interspersed Short Palindromic Repeats (CRISPR)/CRISPR-associated (Cas) systems or components of such systems to modify a genome within a cell. CRISPR/Cas systems include transcripts and other elements involved in the sion of, or directing the activity of, Cas genes. A CRISPR/Cas system can be a type I, a type II, or a type 111 system.

The methods and compositions disclosed herein employ CRISPR/Cas systems by utilizing CRISPR xes (comprising a guide RNA (gRNA) complexed with a Cas protein) for site-directed cleavage of nucleic acids.

Some CRISPR/Cas systems used in the methods disclosed herein are non- naturally occurring. A aturally occurring” system es anything indicating the involvement of the hand of man, such as one or more ents of the system being altered or mutated from their lly occurring state, being at least substantially free from at least one other component with which they are naturally associated in nature, or being associated with at least one other component with which they are not naturally associated. For example, some CRISPR/Cas systems employ non-naturally occurring CRISPR complexes comprising a gRNA and a Cas protein that do not naturally occur together. (i) A. Cas RNA-Guided cleases Cas proteins generally comprise at least one RNA recognition or binding domain. Such domains can interact with guide RNAs (gRNAs, described in more detail below). Cas proteins can also comprise nuclease domains (e.g., DNase or RNase s), DNA binding domains, helicase domains, protein-protein interaction domains, dimerization domains, and other domains. A nuclease domain possesses tic activity for nucleic acid cleavage. Cleavage es the breakage of the covalent bonds of a nucleic acid le.

Cleavage can e blunt ends or staggered ends, and it can be single-stranded or double- stranded.

Examples of Cas proteins include Casl, CaslB, Cas2, Cas3, Cas4, Cas5, Cas5e (CasD), Cas6, Cas6e, Cas6f, Cas7, Cas8al or , Cas8a2, Cas8b, Cas8c, Cas9 (Csnl Csx12), Cale, Caled, CasF, CasG, CasH, Csyl, Csy2, Csy3, Csel (CasA), Cse2 (CasB), Cse3 (CasE), Cse4 , Cscl, Csc2, Csa5, Csn2, Csm2, Csm3, Csm4, Csm5, Csm6, Cmrl , Cmr3, Cmr4, Cmr5, Cmr6, Csbl, Csb2, Csb3, Csxl7, Csxl4, CsxlO, Csxl6, CsaX, Csx3, Csxl, Csx15, Csfl, Csf2, Csf3, Csf4, and Cul966, and homologs or modified versions thereof.

Cas proteins can be from a type II CRISPR/Cas system. For example, the Cas protein can be a Cas9 protein or be derived from a Cas9 protein. Cas9 proteins typically share four key motifs with a conserved ecture. Motifs l, 2, and 4 are Rqu-like , and motif 3 is an HNH motif. The Cas9 protein can be from, for example, Streptococcus pyogenes, Streptococcus thermophilus, Streptococcus sp., Staphylococcus aureus, Nocardiopsis dassonvillei, Streptomyces pristinaespiralis, omyces viridochromogenes, Streptomyces chromogenes, Streptosporangium roseum, Streptosporangium roseum, AlicyclobacHlus acidocaldarius, us pseudomycoides, Bacillus selenitireducens, Exiguobacterium cum, Lactobacillus delbrueckii, Lactobacillus salivarius, Microscilla , Burkholderiales bacterium, Polaromonas naphthalenivorans, monas sp., Crocosphaera watsonii, Cyanothece sp., Microcystis aeruginosa, Synechococcus sp., Acetohalobium arabaticum, Ammonifex degensii, Caldicelulosiruptor becscii, Candidatus Desulforudis, Clostridium botulinum, Clostridium diﬂicile, ldia magna, Natranaerobius thermophilus, Pelotomaculum thermopropionicum, Acidithiobacillus caldus, Acidithiobacillusferrooxidans, Allochromatium vinosum, Marinobacter sp., Nitrosococcus halophilus, Nitrosococcus watsoni, Pseudoalteromonas haloplanktis, Ktedonobacter racemifer, Methanohalobium gatum, Anabaena variabilis, Nodularia spumigena, Nostoc sp., Arthrospira maxima, Arthrospira platensis, spira sp., Lyngbya sp., Microcoleus chthonoplastes, Oscillatoria sp., Petrotoga s, Thermosipho africanus, or Acaryochloris marina. Additional examples of the Cas9 family members are described in WC 2014/131833, herein incorporated by reference in its ty. Cas9 protein from S. pyogenes or d therefrom is a preferred enzyme. Cas9 protein from S. es is assigned SwissProt accession number .

Cas proteins can be wild type proteins (i.e., those that occur in nature), modified Cas proteins (i.e., Cas protein variants), or fragments of wild type or modified Cas proteins. Cas proteins can also be active variants or fragments of wild type or modified Cas proteins. Active variants or fragments can comprise at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to the wild type or modified Cas protein or a portion thereof, wherein the active variants retain the y to cut at a desired cleavage site and hence retain nick-inducing or -strand-break-inducing activity. Assays for nick-inducing or double-strand-break-inducing activity are known and generally measure the overall ty and specificity of the Cas protein on DNA substrates containing the cleavage site.

Cas proteins can be modified to increase or decrease nucleic acid binding affinity, nucleic acid binding specificity, and/or enzymatic activity. Cas proteins can also be modified to change any other activity or property of the protein, such as stability. For example, one or more nuclease domains of the Cas protein can be modified, deleted, or vated, or a Cas protein can be truncated to remove domains that are not essential for the function of the protein or to optimize (e. g., enhance or reduce) the activity of the Cas protein.

Some Cas proteins se at least two nuclease domains, such as DNase domains. For example, a Cas9 n can comprise a Rqu-like se domain and an HNH-like nuclease domain. The Rqu and HNH domains can each cut a different strand of double-stranded DNA to make a double-stranded break in the DNA. See, e. g., Jinek et al. (2012) Science 337:816-821, hereby incorporated by reference in its entirety.

One or both of the nuclease s can be deleted or d so that they are no longer functional or have reduced nuclease activity. If one of the se domains is deleted or mutated, the resulting Cas protein (e. g., Cas9) can be referred to as a nickase and can generate a single-strand break at a CRISPR RNA recognition sequence within a double- ed DNA but not a double-strand break (i.e., it can cleave the complementary strand or the non-complementary strand, but not both). If both of the se domains are deleted or mutated, the resulting Cas n (e. g., Cas9) will have a reduced ability to cleave both s of a double-stranded DNA. An example of a mutation that converts Cas9 into a nickase is a DlOA (aspartate to alanine at position 10 of Cas9) mutation in the Rqu domain of Cas9 from S. pyogenes. Likewise, H939A (histidine to alanine at amino acid position 839) or H840A (histidine to alanine at amino acid position 840) in the HNH domain of Cas9 from S. pyogenes can convert the Cas9 into a nickase. Other examples of mutations that convert Cas9 into a nickase include the corresponding mutations to Cas9 from S. thermophilus. See, e. g., Sapranauskas et a1. (2011) Nucleic Acids Research 39:9275-9282 and WC 2013/141680, each of which is herein orated by reference in its entirety. Such ons can be generated using methods such as irected mutagenesis, PCR-mediated mutagenesis, or total gene synthesis. Examples of other mutations creating nickases can be found, for example, in WO/2013/176772Al and WO/2013/142578Al, each of which is herein incorporated by reference.

Cas proteins can also be fusion proteins. For example, a Cas protein can be fused to a cleavage domain, an epigenetic modification domain, a transcriptional activation domain, or a riptional repressor . See WO 89290, incorporated herein by reference in its entirety. Cas proteins can also be fused to a heterologous polypeptide providing sed or decreased stability. The fused domain or heterologous polypeptide can be located at the N-terminus, the C-terminus, or internally within the Cas protein.

A Cas protein can be fused to a heterologous ptide that provides for subcellular localization. Such heterologous peptides e, for example, a nuclear localization signal (NLS) such as the SV40 NLS for targeting to the s, a mitochondrial localization signal for targeting to the mitochondria, an ER retention signal, and the like.

See, e.g., Lange et a1. (2007) J. Biol. Chem. 282:5101-5105. Such lular localization s can be located at the inus, the C-terminus, or anywhere within the Cas protein.

An NLS can comprise a stretch of basic amino acids, and can be a monopartite sequence or a bipartite sequence.

Cas proteins can also be linked to a cell-penetrating domain. For e, the cell-penetrating domain can be derived from the HIV-1 TAT protein, the TLM cell- penetrating motif from human hepatitis B virus, MPG, Pep-l, VP22, a cell penetrating peptide from Herpes simplex virus, or a polyarginine peptide sequence. See, for example, , herein incorporated by reference in its entirety. The cell-penetrating domain can be located at the N-terminus, the C-terminus, or anywhere within the Cas protein.

Cas proteins can also se a heterologous polypeptide for ease of tracking or purification, such as a ﬂuorescent protein, a purification tag, or an epitope tag. es of ﬂuorescent proteins include green ﬂuorescent proteins (e. g., GFP, GFP-2, tagGFP, turboGFP, eGFP, Emerald, Azami Green, Monomeric Azami Green, CopGFP, AceGFP, ZsGreenl), yellow ﬂuorescent proteins (e. g., YFP, eYFP, Citrine, Venus, YPet, PhiYFP, ZsYellowl), blue cent proteins (e.g. eBFP, eBFPZ, Azurite, mKalamal, GFPuv, Sapphire, T-sapphire), cyan ﬂuorescent proteins (e.g. eCFP, Cerulean, CyPet, AmCyanl, Midoriishi-Cyan), red ﬂuorescent proteins (mKate, mKate2, mPlum, DsRed monomer, mCherry, mRFPl, DsRed-Express, DsRed2, DsRed-Monomer, HcRed-Tandem, HcRedl, AsRed2, eqFP6ll, mRaspberry, mStrawberry, Jred), orange ﬂuorescent proteins (mOrange, mKO, Kusabira-Orange, ric Kusabira-Orange, mTangerine, o), and any other suitable ﬂuorescent protein. Examples of tags include glutathione-S-transferase (GST), chitin binding protein (CBP), e binding protein, thioredoxin (TRX), p01y(NANP), tandem affinity purification (TAP) tag, myc, ACV5, AU1 , AU5, E, ECS, E2, FLAG, hemagglutinin (HA), nus, Softag 1, Softag 3, Strep, SBP, Glu-Glu, HSV, KT3, S, S1 , T7, V5, VSV-G, histidine (His), biotin carboxyl carrier protein (BCCP), and calmodulin.

Cas proteins can be provided in any form. For example, a Cas n can be provided in the form of a protein, such as a Cas protein complexed with a gRNA.

Alternatively, a Cas protein can be provided in the form of a nucleic acid encoding the Cas protein, such as an RNA (e. g., messenger RNA (mRNA)) or DNA. Optionally, the nucleic acid encoding the Cas protein can be codon optimized for efficient translation into protein in a ular cell or organism.

Nucleic acids encoding Cas proteins can be stably integrated in the genome of the cell and operably linked to a promoter active in the cell. Alternatively, c acids encoding Cas ns can be operably linked to a promoter in an expression construct.

Expression constructs e any nucleic acid constructs e of directing expression of a gene or other c acid sequence of interest (e.g., a Cas gene) and which can transfer such a nucleic acid sequence of interest to a target cell. Promoters that can be used in an expression construct include, for example, promoters active in a pluripotent rat, eukaryotic, mammalian, non-human mammalian, human, rodent, mouse, or hamster cell. Examples of other promoters are described elsewhere herein. (ii) B. Guide RNAs (gRNAs) A “guide RNA” or “gRNA” includes an RNA molecule that binds to a Cas protein and targets the Cas protein to a specific location within a target DNA. Guide RNAs can comprise two segments: a “DNA-targeting segment” and a “protein-binding segment.” “Segment” includes a segment, section, or region of a molecule, such as a contiguous stretch of nucleotides in an RNA. Some gRNAs comprise two separate RNA molecules: an “activator-RNA” and a “targeter-RNA.” Other gRNAs are a single RNA molecule (single RNA polynucleotide), which can also be called a “single-molecule gRNA,” a “single-guide RNA,” or an “ngNA.” See, e.g., WO/2013/176772A1, WO/2014/065596A1, WO/2014/089290A1, WO/2014/093622A2, WO/2014/099750A2, WO/2013142578A1, and WC 31833A1, each of which is herein orated by reference. The terms “guide RNA” and “gRNA” include both double-molecule gRNAs and single-molecule gRNAs.

An exemplary lecule gRNA comprises a chNA-like (“CRISPR RNA” or ter-RNA” or “chNA” or “chNA ”) molecule and a corresponding A- like (“trans-acting CRISPR RNA” or “activator-RNA” or “trachNA” or “scaffold”) le. A chNA comprises both the DNA-targeting segment (single-stranded) of the gRNA and a stretch of nucleotides that forms one half of the dsRNA duplex of the protein- binding segment of the gRNA.

A corresponding trachNA (activator-RNA) comprises a stretch of nucleotides that forms the other half of the dsRNA duplex of the protein-binding segment of the gRNA.

A stretch of nucleotides of a chNA are mentary to and hybridize with a stretch of tides of a trachNA to form the dsRNA duplex of the protein-binding domain of the gRNA. As such, each chNA can be said to have a corresponding trachNA.

The chNA and the corresponding trachNA hybridize to form a gRNA. The chNA additionally es the single-stranded rgeting segment that hybridizes to a CRISPR RNA recognition sequence. If used for modification within a cell, the exact sequence of a given chNA or trachNA molecule can be designed to be ic to the species in which the RNA molecules will be used. See, for example, Mali et al. (2013) Science 339:823-826; Jinek et al. (2012) Science 337:816-821; Hwang et al. (2013) Nat.

Biotechnol. 31:227-229; Jiang et al. (2013) Nat. Biotechnol. 31 :233-239; and Cong et al. (2013) Science 339:819-823, each of which is herein incorporated by reference.

The DNA-targeting segment (chNA) of a given gRNA comprises a nucleotide sequence that is complementary to a sequence in a target DNA. The DNA- targeting segment of a gRNA cts with a target DNA in a sequence-specific manner via hybridization (i.e., base pairing). As such, the nucleotide sequence of the DNA-targeting segment may vary and determines the location within the target DNA with which the gRNA and the target DNA will interact. The DNA-targeting segment of a t gRNA can be modified to hybridize to any desired sequence within a target DNA. Naturally occurring chNAs differ depending on the Cas9 system and sm but often contain a targeting segment of n 21 to 72 nucleotides length, ﬂanked by two direct repeats (DR) of a length of between 21 to 46 nucleotides (see, e. g., WO2014/131833). In the case of S. pyogenes, the DRs are 36 nucleotides long and the targeting segment is 30 tides long.

The 3’ located DR is complementary to and izes with the corresponding trachNA, which in turn binds to the Cas9 protein.

The DNA-targeting segment can have a length of from about 12 nucleotides to about 100 nucleotides. For example, the DNA-targeting segment can have a length of from about 12 nucleotides (nt) to about 80 nt, from about 12 nt to about 50 nt, from about 12 nt to about 40 nt, from about 12 nt to about 30 nt, from about 12 nt to about 25 nt, from about 12 nt to about 20 nt, or from about 12 nt to about 19 nt. Alternatively, the DNA-targeting WO 00805 segment can have a length of from about 19 nt to about 20 nt, from about 19 nt to about 25 nt, from about 19 nt to about 30 nt, from about 19 nt to about 35 nt, from about 19 nt to about 40 nt, from about 19 nt to about 45 nt, from about 19 nt to about 50 nt, from about 19 nt to about 60 nt, from about 19 nt to about 70 nt, from about 19 nt to about 80 nt, from about 19 nt to about 90 nt, from about 19 nt to about 100 nt, from about 20 nt to about 25 nt, from about 20 nt to about 30 nt, from about 20 nt to about 35 nt, from about 20 nt to about 40 nt, from about nt to about 45 nt, from about 20 nt to about 50 nt, from about 20 nt to about 60 nt, from about 20 nt to about 70 nt, from about 20 nt to about 80 nt, from about 20 nt to about 90 nt, or from about 20 nt to about 100 nt.

The nucleotide sequence of the DNA-targeting segment that is complementary to a nucleotide sequence R RNA recognition sequence) of the target DNA can have a length at least about 12 nt. For example, the rgeting sequence (i.e., the sequence within the DNA-targeting segment that is complementary to a CRISPR RNA ition sequence within the target DNA) can have a length at least about 12 nt, at least about 15 nt, at least about 18 nt, at least about 19 nt, at least about 20 nt, at least about 25 nt, at least about nt, at least about 35 nt, or at least about 40 nt. Alternatively, the DNA-targeting sequence can have a length of from about 12 nucleotides (nt) to about 80 nt, from about 12 nt to about 50 nt, from about 12 nt to about 45 nt, from about 12 nt to about 40 nt, from about 12 nt to about 35 nt, from about 12 nt to about 30 nt, from about 12 nt to about 25 nt, from about 12 nt to about 20 nt, from about 12 nt to about 19 nt, from about 19 nt to about 20 nt, from about 19 nt to about 25 nt, from about 19 nt to about 30 nt, from about 19 nt to about 35 nt, from about 19 nt to about 40 nt, from about 19 nt to about 45 nt, from about 19 nt to about 50 nt, from about 19 nt to about 60 nt, from about 20 nt to about 25 nt, from about 20 nt to about 30 nt, from about 20 nt to about 35 nt, from about 20 nt to about 40 nt, from about 20 nt to about 45 nt, from about 20 nt to about 50 nt, or from about 20 nt to about 60 nt. In some cases, the DNA-targeting sequence can have a length of at about 20 nt.

TrachNAs can be in any form (e.g., full-length trachNAs or active partial trachNAs) and of varying lengths. They can include primary transcripts or processed forms.

For example, trachNAs (as part of a single-guide RNA or as a separate molecule as part of a lecule gRNA) may comprise or consist of all or a portion of a wild-type trachNA sequence (e.g., about or more than about 20, 26, 32, 45, 48, 54, 63, 67, 85, or more nucleotides of a wild-type trachNA sequence). Examples of wild-type trachNA sequences from S. pyogenes e 171-nucleotide, 89-nucleotide, 75-nucleotide, and 65-nucleotide versions. See, for example, Deltcheva et a1. (2011) Nature 471 :602-607; , each of which is incorporated herein by nce in their entirety. es of trachNAs within -guide RNAs (ngNAs) e the A segments found within +48, +54, +67, and +85 versions of ngNAs, where “+n” indicates that up to the +n nucleotide of wild- type trachNA is included in the ngNA. See US 8,697,359, incorporated herein by reference in its entirety.

The percent complementarity between the DNA-targeting sequence and the CRISPR RNA recognition sequence within the target DNA can be at least 60% (e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%). The t complementarity between the DNA- targeting ce and the CRISPR RNA recognition ce within the target DNA can be at least 60% over about 20 contiguous tides. As an example, the percent mentarity between the DNA-targeting sequence and the CRISPR RNA recognition sequence within the target DNA is 100% over the 14 contiguous nucleotides at the 5’ end of the CRISPR RNA recognition sequence within the mentary strand of the target DNA and as low as 0% over the remainder. In such a case, the DNA-targeting sequence can be considered to be 14 nucleotides in length. As another example, the percent complementarity between the DNA-targeting sequence and the CRISPR RNA recognition sequence within the target DNA is 100% over the seven contiguous nucleotides at the 5’ end of the CRISPR RNA recognition sequence within the complementary strand of the target DNA and as low as 0% over the remainder. In such a case, the DNA-targeting sequence can be considered to be 7 nucleotides in length.

The protein-binding segment of a gRNA can comprise two stretches of nucleotides that are complementary to one another. The complementary nucleotides of the protein-binding t hybridize to form a double-stranded RNA duplex (dsRNA). The protein-binding segment of a subject gRNA interacts with a Cas protein, and the gRNA directs the bound Cas protein to a ic nucleotide sequence within target DNA via the DNA-targeting segment.

Guide RNAs can include modifications or sequences that provide for additional desirable features (e. g., modified or regulated stability; subcellular targeting; tracking with a cent label; a binding site for a protein or protein complex; and the like). Examples of such modifications include, for example, a 5' cap (e. g., a 7- methylguanylate cap (m7G)); a 3' polyadenylated tail (i.e., a 3' poly(A) tail); a riboswitch sequence (e. g., to allow for regulated stability and/or regulated accessibility by proteins and/or protein complexes); a stability control sequence; a sequence that forms a dsRNA duplex (i.e., a hairpin)); a modification or sequence that targets the RNA to a subcellular location (e. g., nucleus, mitochondria, chloroplasts, and the like); a modification or sequence that provides for ng (e. g., direct conjugation to a ﬂuorescent molecule, conjugation to a moiety that facilitates ﬂuorescent detection, a sequence that allows for ﬂuorescent detection, and so forth); a modification or sequence that provides a binding site for proteins (e. g., proteins that act on DNA, including transcriptional activators, transcriptional repressors, DNA transferases, DNA demethylases, histone acetyltransferases, histone deacetylases, and the like); and combinations thereof.

Guide RNAs can be provided in any form. For example, the gRNA can be ed in the form of RNA, either as two molecules (separate chNA and trachNA) or as one molecule (ngNA), and optionally in the form of a complex with a Cas protein. The gRNA can also be provided in the form of DNA encoding the RNA. The DNA encoding the gRNA can encode a single RNA molecule (ngNA) or separate RNA molecules (e.g., separate chNA and trachNA). In the latter case, the DNA encoding the gRNA can be provided as separate DNA les encoding the chNA and trachNA, respectively.

DNAs encoding gRNAs can be stably integrated in the genome of the cell and operably linked to a promoter active in the cell. Alternatively, DNAs encoding gRNAs can be operably linked to a promoter in an expression construct. Such ers can be active, for example, in a pluripotent rat, eukaryotic, mammalian, non-human mammalian, human, rodent, mouse, or hamster cell. In some instances, the promoter is an RNA polymerase III promoter, such as a human U6 er, a rat U6 polymerase III er, or a mouse U6 polymerase III promoter. Examples of other promoters are described elsewhere .

Alternatively, gRNAs can be prepared by various other methods. For e, gRNAs can be prepared by in vitro transcription using, for example, T7 RNA polymerase (see, for example, and ). Guide RNAs can also be a synthetically produced molecule prepared by chemical synthesis. (iii) C. CRISPR RNA ition Sequences The term "CRISPR RNA recognition sequence" includes nucleic acid sequences t in a target DNA to which a rgeting segment of a gRNA will bind, provided sufficient conditions for binding exist. For example, CRISPR RNA ition ces include sequences to which a guide RNA is designed to have complementarity, where hybridization between a CRISPR RNA recognition ce and a DNA targeting sequence promotes the formation of a CRISPR complex. Full complementarity is not necessarily required, provided there is ient complementarity to cause hybridization and promote formation of a CRISPR complex. CRISPR RNA recognition sequences also include cleavage sites for Cas proteins, described in more detail below. A CRISPR RNA recognition sequence can comprise any polynucleotide, which can be d, for example, in the nucleus or cytoplasm of a cell or within an organelle of a cell, such as a mitochondrion or chloroplast.

The CRISPR RNA ition sequence within a target DNA can be targeted by (i.e., be bound by, or hybridize with, or be complementary to) a Cas protein or a gRNA. le DNA/RNA g conditions include physiological conditions normally present in a cell. Other suitable DNA/RNA binding conditions (e.g., conditions in a cell-free system) are known in the art (see, e. g., Molecular Cloning: A tory Manual, 3rd Ed. (Sambrook et al., Harbor Laboratory Press 2001)). The strand of the target DNA that is complementary to and hybridizes with the Cas protein or gRNA can be called the "complementary strand," and the strand of the target DNA that is complementary to the "complementary strand" (and is therefore not complementary to the Cas protein or gRNA) can be called "noncomplementary strand" or ate strand.” The Cas n can cleave the nucleic acid at a site within or outside of the nucleic acid ce present in the target DNA to which the rgeting segment of a gRNA will bind. The “cleavage site” includes the position of a nucleic acid at which a Cas protein produces a single-strand break or a -strand break. For e, formation of a CRISPR x (comprising a gRNA hybridized to a CRISPR RNA recognition sequence and xed with a Cas protein) can result in cleavage of one or both strands in or near (e.g., within 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 50, or more base pairs from) the nucleic acid sequence present in a target DNA to which a DNA-targeting segment of a gRNA will bind.

If the cleavage site is outside of the nucleic acid sequence to which the DNA-targeting segment of the gRNA will bind, the ge site is still considered to be within the “CRISPR RNA recognition sequence.” The cleavage site can be on only one strand or on both strands of a nucleic acid. Cleavage sites can be at the same position on both strands of the nucleic acid (producing blunt ends) or can be at ent sites on each strand (producing staggered ends). Staggered ends can be produced, for example, by using two Cas proteins, each of which produces a single-strand break at a different cleavage site on each strand, thereby producing a double-strand break. For example, a first nickase can create a single-strand break on the first strand of double-stranded DNA (dsDNA), and a second nickase can create a single-strand break on the second strand of dsDNA such that overhanging sequences are created. In some cases, the CRISPR RNA recognition sequence of the nickase on the first strand is separated from the CRISPR RNA recognition sequence of the nickase on the second strand by at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 40, 50, 75, 100, 250, 500, or 1,000 base pairs.

Site-specific cleavage of target DNA by Cas9 can occur at locations determined by both (i) base-pairing complementarity between the gRNA and the target DNA and (ii) a short motif, called the pacer adjacent motif (PAM), in the target DNA. The PAM can ﬂank the CRISPR RNA recognition sequence. Optionally, the CRISPR RNA ition sequence can be ﬂanked by the PAM. For example, the cleavage site of Cas9 can be about 1 to about 10 or about 2 to about 5 base pairs (e. g., 3 base pairs) upstream or downstream of the PAM sequence. In some cases (e. g., when Cas9 from S. pyogenes or a y related Cas9 is used), the PAM sequence of the non-complementary strand can be 5'- N1GG-3', where N1is any DNA nucleotide and is immediately 3' of the CRISPR RNA recognition sequence of the non-complementary strand of the target DNA. As such, the PAM sequence of the complementary strand would be 5'-CC N2-3', where N2 is any DNA nucleotide and is immediately 5' of the CRISPR RNA recognition sequence of the complementary strand of the target DNA. In some such cases, N1 and N2 can be complementary and the N1- N2 base pair can be any base pair (e. g., N1=C and N2=G; N1=G and N2=C; N1=A and N2=T, N1=T, and N2=A).

Examples of CRISPR RNA recognition sequences include a DNA sequence mentary to the DNA-targeting segment of a gRNA, or such a DNA sequence in addition to a PAM sequence. For example, the target motif can be a 20-nucleotide DNA sequence immediately preceding an NGG motif recognized by a Cas protein (see, for example, WC 2014/165825). The guanine at the 5’ end can facilitate transcription by RNA rase in cells. Other examples of CRISPR RNA recognition sequences can include two guanine tides at the 5’ end (e. g., GGNZONGG; SEQ ID NO: 9) to facilitate efficient ription by T7 polymerase in vitro. See, for e, WO 65596.

The CRISPR RNA recognition sequence can be any nucleic acid ce endogenous or exogenous to a cell. The CRISPR RNA ition sequence can be a sequence coding a gene product (e. g., a protein) or a non-coding sequence (e. g., a regulatory sequence) or can include both.

In one embodiment, the target sequence is immediately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence. In one embodiment, the locus of interest comprises the nucleotide sequence of SEQ ID NO: 1. In one embodiment, the gRNA comprises a third nucleic acid sequence encoding a Clustered rly Interspaced Short Palindromic Repeats (CRISPR) RNA (chNA) and a trans-activating CRISPR RNA (trachNA). In another WO 00805 embodiment, the genome of the pluripotent rat cell comprises a target DNA region complementary to the target sequence. In some such methods, the Cas protein is Cas9. In some embodiments, the gRNA ses (a) the chimeric RNA of the nucleic acid sequence of SEQ ID NO: 2; or (b) the ic RNA of the c acid sequence of SEQ ID NO: 3.

In some such methods, the chNA comprises the sequence set forth in SEQ ID NO: 4, SEQ ID NO: 5, or SEQ ID NO: 6. In some such methods, the trachNA comprises the sequence set forth in SEQ ID NO: 7 or SEQ ID NO: 8.

Active variants and fragments of nuclease agents (i.e. an ered nuclease agent) are also provided. Such active variants can comprise at least 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to the native nuclease agent, wherein the active variants retain the ability to cut at a d recognition site and hence retain nick or double-strand-break-inducing activity. For example, any of the nuclease agents described herein can be modified from a native endonuclease sequence and designed to recognize and induce a nick or -strand break at a recognition site that was not recognized by the native nuclease agent. Thus, in some embodiments, the engineered nuclease has a specificity to induce a nick or double-strand break at a recognition site that is different from the corresponding native nuclease agent recognition site. Assays for nick or double-strand-break-inducing activity are known and generally measure the overall activity and specificity of the endonuclease on DNA substrates containing the recognition site.

The nuclease agent may be introduced into the cell by any means known in the art.

The polypeptide encoding the nuclease agent may be directly introduced into the cell.

Alternatively, a polynucleotide encoding the nuclease agent can be introduced into the cell.

When a cleotide encoding the nuclease agent is introduced into the cell, the nuclease agent can be transiently, conditionally or constitutive expressed within the cell. Thus, the cleotide encoding the nuclease agent can be contained in an expression cassette and be operably linked to a conditional promoter, an inducible promoter, a constitutive promoter, or a tissue-specific promoter. Such promoters of interest are discussed in further detail elsewhere . Alternatively, the nuclease agent is introduced into the cell as an mRNA encoding a nuclease agent.

In specific ments, the cleotide encoding the nuclease agent is stably integrated in the genome of the cell and ly linked to a promoter active in the cell. In other embodiments, the polynucleotide encoding the nuclease agent is in the same targeting vector comprising the insert cleotide, while in other instances the polynucleotide encoding the nuclease agent is in a vector or a plasmid that is separate from the targeting vector comprising the insert polynucleotide.

When the nuclease agent is ed to the cell through the introduction of a polynucleotide encoding the nuclease agent, such a polynucleotide encoding a nuclease agent can be modified to substitute codons having a higher frequency of usage in the cell of st, as compared to the naturally ing polynucleotide ce encoding the nuclease agent. For example the polynucleotide encoding the nuclease agent can be modified to substitute codons having a higher frequency of usage in a given prokaryotic or eukaryotic cell of interest, including a bacterial cell, a yeast cell, a human cell, a non-human cell, a mammalian cell, a rodent cell, a mouse cell, a rat cell or any other host cell of interest, as compared to the naturally occurring polynucleotide sequence.

B. Employing the CRISPR/Cas System in Combination with a Large Targeting Vector (LTVEC) or a Small Targeting Vector (SmallTVEC) to Modify a Challenging Genomic Loci or a Y Chromosome Locus ] Non-limiting methods for modifying a nging genomic locus or a locus of the Y chromosome comprise exposing the chromosome (i.e., the Y chromosome) to a Cas protein and a CRISPR RNA in the ce of a large targeting vector (LTVEC) comprising a c acid sequence of at least 10 kb, wherein following exposure to the Cas protein, the CRISPR RNA, and the LTVEC, the chromosome (i.e., the Y chromosome) is modified to contain at least 10 kb nucleic acid sequence.

The method can employ any of the LTVECs or VECs described herein. In non-limiting embodiments, the LTVEC or smallTVEC comprises a nucleic acid sequence of at least 20 kb, at least 30 kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, at least 90 kb, at least 100 kb, at least 150 kb, or at least 200 kb. In other embodiments, the sum total of 5’ and 3’ homology arms of the LTVEC is from about 10 kb to about 150 kb, about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 120 kb, or from about 120 kb to 150 kb. In another embodiment, the sum total of 5’ and 3’ homology arms of the smallTVEC is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb.

Further provided is a method for modifying a challenging target locus or a target genomic locus on the Y chromosome, sing: (a) providing a mammalian cell comprising the challenging target locus or a target genomic locus on the Y some, wherein the target genomic locus comprises a guide RNA (gRNA) target sequence; (b) introducing into the mammalian cell: (i) a large targeting vector (LTVEC) comprising a first nucleic acid ﬂanked with ing arms homologous to the target genomic locus, wherein the LTVEC is at least 10 kb; (ii) a first expression construct comprising a first promoter operably linked to a second nucleic acid encoding a Cas protein, and (iii) a second sion construct sing a second promoter operably linked to a third nucleic acid encoding a guide RNA (gRNA) comprising a nucleotide sequence that hybridizes to the gRNA target ce and a trans-activating CRISPR RNA (trachNA), wherein the first and the second promoters are active in the mammalian cell; and, (c) identifying a modified mammalian cell comprising a targeted genetic cation at the challenging target genomic locus or at the target genomic locus on the Y some. In specific embodiments, the first and the second expression constructs are on a single nucleic acid molecule. In other embodiments, the target genomic locus of the Y chromosomes is the Sry locus.

As outlined above, in one embodiment, the Cas protein can comprise a Cas9 protein. In another embodiment, the gRNA target sequence is immediately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence.

The method can employ any of the LTVECs or smallTVECs described herein. In miting embodiments, the LTVEC or smallTVEC is at least 0.5 kb, at least 1 kb, at least kb, at least 10 kb, at least 15 kb, at least 20 kb, at least 30kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, at least 90 kb, at least 100 kb, at least 150 kb, or at least 200 kb. In other embodiments, the sum total of 5’ and 3’ homology arms of the LTVEC is from about 10 kb to about 150 kb, about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 120 kb, or from about 120 kb to 150 kb.

The various methods employing the CRISPR/Cas system (or any method disclosed herein) can be performed on, for example, mammalian cells, non-human mammalian cells, fibroblast cells, rodent cells, rat cells, mouse cells, or hamster cells. The cell can be a pluripotent cell, an d pluripotent stem (iPS) cell, a mouse embryonic stem (ES) cell, a rat embryonic stem (ES) cell, a human embryonic stem (ES) cell or a developmentally restricted human progenitor cell.

As discussed in detail below, following the modification a challenging genomic locus or a genomic locus of interest on the Y chromosome (i.e., the Sry locus) of a non- human pluripotent cell ing, for example, using the CRISPR/CAS system outline above, the genetically modified non-human otent cell that is produced can be introduced into a non-human host embryo; and the non-human host embryo comprising the modified pluripotent cell in a surrogate mother is gestated. The surrogate mother es F0 progeny comprising the targeted genetic modification. In specific embodiments, the targeted genetic modification is capable of being itted through the germline.

C. Selection Markers Various selection markers can be used in the methods and itions disclosed herein which provide for modifying a target genomic locus on the Y some or a challenging target genomic locus. Such markers are disclosed elsewhere herein and include, but are not limited to, selection markers that impart resistance to an antibiotic such as G418, hygromycin, blastocidin, neomycin, or puromycin. The polynucleotide encoding the selection markers are operably linked to a promoter active in the cell. Such expression cassettes and their various regulatory components are discussed in further detailed elsewhere herein.

D. Target c Locus Various methods and compositions are provided which allow for the integration of at least one insert polynucleotide at a target genomic locus on the Y chromosome or a challenging target genomic locus. As used herein, a “target c locus on the Y some” comprises any t or region of DNA on the Y chromosome that one desires to integrate an insert polynucleotide.

The genomic locus on the Y chromosome or a challenging target genomic locus being targeted can be native to the cell, or alternatively can comprise a heterologous or exogenous t of DNA that was integrated into the chromosome of the cell. Such heterologous or ous ts of DNA can include transgenes, expression cassettes, polynucleotide encoding ion makers, or heterologous or exogenous regions of genomic DNA. The target genomic locus on the Y chromosome or the challenging target genomic locus can comprise any of the targeted genomic ation system including, for example, the recognition site, the selection marker, previously integrated insert polynucleotides, polynucleotides encoding nuclease agents, ers, etc. Alternatively, the target genomic locus on the Y chromosome or the challenging target genomic locus can be located within a yeast artificial chromosome (YAC), bacterial artificial chromosome (BAC), a human artificial chromosome, or any other engineered genomic region contained in an appropriate host cell. Thus, in specific embodiments, the targeted genomic locus on the Y chromosome or the challenging target genomic locus can comprise native, heterologous or exogenous genomic nucleic acid sequence from a non-human mammal, a non-human cell, a rodent, a human, a rat, a mouse, a hamster, a rabbit, a pig, a , a deer, a sheep, a goat, a chicken, a cat, a dog, a ferret, a primate (e. g., marmoset, rhesus monkey), domesticated mammal or an agricultural mammal or any other organism of interest or a combination thereof.

Non-limiting examples of the target genomic locus on the Y chromosome include, the Sry gene, the Uty gene, the Eif2s3y gene, the Ddx3y gene, the gene, the Ubely gene, the Tspy gene, the Usp9y gene, the ny1 gene, and the ny2 gene and the region on the Y chromosome encompassing the Kdm5d, Eif2s3y, Tspy, Uty, Ddx3y, and Usp9y genes. Such a locus on the Y chromosome can be from a non-human mammal, a mammal, a rodent, a human, a rat, a mouse, a hamster, a , a pig, a , a deer, a sheep, a goat, a chicken, a cat, a dog, a ferret, a primate (e. g., marmoset, rhesus monkey), domesticated mammal or an ltural mammal or any other organism of interest or a combination thereof. Such cells include pluripotent cells, including, for example, induced pluripotent stem (iPS) cells, mouse embryonic stem (ES) cells, rat embryonic stem (ES) cells, human embryonic stem (ES) cell, or developmentally restricted human progenitor cells.

As described elsewhere , s methods and compositions are provided which comprise XY pluripotent and/or totipotent cells (such as XY ES cells or iPS cells) having a decreased activity or level of the Sry protein. The various methods described herein to modify genomic locus on the Y chromosome can also be used to uce ed genetic modifications to polynucleotides of interest that are not located on the Y chromosome.

E. Targeting Vectors and Insert cleotides As ed above, methods and itions provided herein employ ing vectors alone or in combination with a nuclease agent. “Homologous recombination” is used conventionally to refer to the exchange of DNA fragments between two DNA molecules at over sites within the regions of homology. 1'. Insert Polynucleotide As used herein, the “insert polynucleotide” comprises a t of DNA that one desires to integrate at the target genomic locus. In specific embodiments, the target genomic locus is on the Y chromosome. In other embodiments, the target genomic locus is a challenging genomic locus. In one embodiment, the insert polynucleotide comprises one or more polynucleotides of interest. In other embodiments, the insert polynucleotide can comprise one or more expression cassettes. A given expression te can comprise a polynucleotide of st, a polynucleotide encoding a selection marker and/or a reporter gene along with the various regulatory ents that inﬂuence expression. miting examples of polynucleotides of interest, selection markers, and reporter genes that can be included within the insert polynucleotide are discussed in detail elsewhere herein.

In specific embodiments, the insert polynucleotide can comprise a genomic nucleic acid. In one embodiment, the genomic c acid is d from an animal, a mouse, a human, a non-human, a rodent, a man, a rat, a hamster, a rabbit, a pig, a bovine, a deer, a sheep, a goat, a chicken, a cat, a dog, a ferret, a primate (e.g., marmoset, rhesus monkey), icated mammal or an agricultural mammal, an avian, or any other organism of interest or a combination thereof.

In further embodiments, the insert polynucleotide comprises a conditional allele.

In one embodiment, the conditional allele is a multifunctional allele, as described in US 2011/0104799, which is incorporated by reference in its entirety. In specific embodiments, the conditional allele comprises: (a) an ing sequence in sense orientation with respect to transcription of a target gene, and a drug ion cassette in sense or antisense orientation; (b) in antisense orientation a nucleotide sequence of interest (NSI) and a conditional by inversion module (COIN, which utilizes an exon-splitting intron and an invertible genetrap- like module; see, for example, US 2011/0104799, which is incorporated by nce in its entirety); and (c) recombinable units that recombine upon re to a first recombinase to form a conditional allele that (i) lacks the actuating sequence and the DSC, and (ii) contains the NSI in sense orientation and the COIN in antisense orientation.

The insert polynucleotide can be from about 5kb to about 200kb, from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 30kb, from about 30kb to about 40kb, from about 40kb to about 50kb, from about 60kb to about 70kb, from about 80kb to about 90kb, from about 90kb to about 100kb, from about 100kb to about 110kb, from about 120kb to about 130kb, from about 130kb to about 140kb, from about 140kb to about 150kb, from about 150kb to about 160kb, from about 160kb to about 170kb, from about 170kb to about 180kb, from about 180kb to about 190kb, from about 190kb to about 200kb, from about 200kb to about 250kb, from about 250kb to about 300kb, from about 300kb to about 350kb, or from about 350kb to about 400kb.

In ic embodiments, the insert polynucleotide comprises a nucleic acid ﬂanked with pecific recombination target sequences. It is recognized that while the entire insert polynucleotide can be ﬂanked by such site-specific recombination target sequence, any region or individual polynucleotide of interest within the insert polynucleotide can also be ﬂanked by such sites. The term "recombination site" as used herein includes a nucleotide sequence that is ized by a site-specific recombinase and that can serve as a substrate for a recombination event. The term "site-specific inase" as used herein includes a group of enzymes that can facilitate recombination between recombination sites where the two recombination sites are physically separated within a single nucleic acid molecule or on separate nucleic acid molecules. es of site-specific inases include, but are not limited to, Cre, Flp, and Dre inases. The site-specific recombinase can be introduced into the cell by any means, including by introducing the recombinase polypeptide into the cell or by ucing a polynucleotide encoding the site- specific recombinase into the host cell. The polynucleotide encoding the site-specific recombinase can be located within the insert polynucleotide or within a separate polynucleotide. The site-specific recombinase can be operably linked to a er active in the cell including, for example, an inducible promoter, a promoter that is nous to the cell, a promoter that is heterologous to the cell, a cell-specific promoter, a tissue-specific promoter, or a developmental stage-specific promoter. Site-specific recombination target sequences which can ﬂank the insert polynucleotide or any polynucleotide of interest in the insert polynucleotide can include, but are not limited to, loxP, lox511, lox2272, lox66, lox71, loxM2, lox5171, FRT, FRTl 1, FRT71, attp, att, FRT, rox, and a combination thereof.

In other embodiments, the site-specific recombination sites ﬂank a polynucleotide encoding a selection marker and/or a reporter gene contained within the insert polynucleotide. In such instances following integration of the insert cleotide at the ed genomic locus the sequences between the site-specific recombination sites can be removed.

In one embodiment, the insert polynucleotide comprises a polynucleotide encoding a selection marker. Such selection markers include, but are not limited, to neomycin phosphotransferase (neor), hygromycin B otransferase (hygr), puromycin-N- acetyltransferase (puror), cidin S deaminase (bsrr), ne/guanine phosphoribosyl erase (gpt), or herpes x virus thymidine kinase (HSV-k), or a combination thereof. In one embodiment, the polynucleotide encoding the selection marker is operably linked to a promoter active in the cell. When serially tiling polynucleotides of interest into a targeted genomic locus, the selection marker can comprise a ition site for a nuclease agent, as outlined above. In one embodiment, the polynucleotide encoding the selection marker is ﬂanked with a pecific recombination target sequences.

The insert polynucleotide can further comprise a reporter gene operably linked to a promoter, wherein the reporter gene encodes a reporter n selected from the group consisting of LacZ, mPlum, mCherry, thomato, mStrawberry, J-Red, DsRed, mOrange, mKO, ne, Venus, YPet, enhanced yellow ﬂuorescent protein (EYFP), Emerald, enhanced green cent protein (EGFP), CyPet, cyan ﬂuorescent n (CFP), Cerulean, T-Sapphire, luciferase, alkaline phosphatase, and a combination thereof. Such reporter genes can be operably linked to a promoter active in the cell. Such promoters can be an inducible promoter, a promoter that is nous to the reporter gene or the cell, a er that is heterologous to the reporter gene or to the cell, a cell-specific promoter, a tissue-specific promoter manner or a developmental stage-specific promoter. ii. Targeting Vectors Targeting vectors are employed to introduce the insert polynucleotide into the targeted genomic locus on the Y chromosome or into a challenging target locus or on another chromosome of interest. The targeting vector comprises the insert polynucleotide and r comprises an upstream and a ream gy arm that ﬂank the insert polynucleotide.

The homology arms that ﬂank the insert polynucleotide correspond to genomic regions within the targeted genomic locus. For ease of reference, the ponding genomic regions within the targeted c locus are referred to herein as “target sites”. Thus, in one example, a targeting vector can comprise a first insert polynucleotide ﬂanked by a first and a second homology arm corresponding to a first and a second target site located in sufficient proximity to the first recognition site within the polynucleotide encoding the selection marker. As such, the targeting vector thereby aids in the integration of the insert polynucleotide into the targeted genomic locus through a homologous recombination event that occurs between the homology arms and the corresponding target sites within the genome of the cell.

A gy arm of the targeting vector can be of any length that is sufficient to promote a homologous recombination event with a corresponding target site, including for 2015/038001 example, from about 400 bp to about 500 bp, from about 500 bp to about 600 bp, from about 600 bp to about 700 bp, from about 700 bp to about 800 bp, from about 800 bp to about 900 bp, or from about 900 bp to about 1000 bp; or at least 5-10, 5-15, 5-20, 5-25, 5-30, 5-35, 5- 40, 5-45, 5- 50, 5-55, 5-60, 5-65, 5- 70, 5-75, 5-80, 5-85, 5-90, 5-95, 5-100, 100-200, or 200- 300 kilobases in length or greater. In specific embodiments, the sum total of the targeting arms is at least 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4kb, 5kb, 6kb, 7kb, 8kb, 9kb or at least 10kb.

In other ments, the sum total of the homology arms is between about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4kb to about 5kb, about 5kb to about 6kb, about 6kb to about 7kb, about 7kb to about 8kb, about 8kb to about 9kb, or about 10kb to about 150kb. As outlined in further detail below, large targeting vectors can employ targeting arms of greater length.

The target sites within the targeted genomic locus that correspond to the am and downstream homology arms of the targeting vector are located in “sufficient proximity to the recognition site” located in the polynucleotide encoding the selection marker. As used herein, the upstream and downstream homology arms of a targeting vector are “located in ient proximity” to a recognition site when the distance is such as to promote the occurrence of a homologous recombination event between the target sites and the homology arms upon a nick or double-strand break at the recognition site. Thus, in specific embodiments, the target sites corresponding to the upstream and/or downstream homology arm of the targeting vector are within at least 10 nucleotide to about 14 kb of a given recognition site. In specific embodiments, the recognition site is immediately adjacent to at least one or both of the target sites.

The spatial relationship of the target sites that correspond to the homology arms of the targeting vector to the recognition site within the cleotide encoding the selection marker can vary. For example, both target sites can be d 5’ to the recognition site, both target sites can be d 3’ to the recognition site, or the target sites can flank the recognition site.

In specific embodiments, the target genomic locus comprises (i) a 5’ target sequence that is homologous to a 5’ gy arm; and (ii) a 3’ target sequence that is homologous to a 3’ homology arm. In specific embodiments, the 5’ target ce and the 3’ target sequence is separated by at least 5 kb but less than 3 Mb, at least 5 kb but less than kb, at least 10 kb but less than 20 kb, at least 20 kb but less than 40 kb, at least 40 kb but less than 60 kb, at least 60 kb but less than 80 kb, at least about 80 kb but less than 100 kb, at least 100 kb but less than 150 kb, or at least 150 kb but less than 200 kb, at least about 200 kb 2015/038001 but less than about 300 kb, at least about 300 kb but less than about 400 kb, at least about 400 kb but less than about 500 kb, at least about 500 kb but less than about 1Mb, at least about 1 Mb but less than about 1.5 Mb, at least about 1.5 Mb but less than about 2 Mb, at least about 2 Mb but less than about 2.5 Mb, or at least about 2.5 Mb but less than about 3 Mb.

As used herein, a homology arm and a target site “correspond” or are “corresponding” to one another when the two regions share a sufficient level of sequence identity to one another to act as substrates for a homologous recombination reaction. By “homology” is meant DNA sequences that are either identical or share sequence identity to a corresponding sequence. The ce identity between a given target site and the corresponding homology arm found on the targeting vector can be any degree of ce identity that allows for homologous recombination to occur. For example, the amount of sequence ty shared by the homology arm of the targeting vector (or a fragment thereof) and the target site (or a fragment thereof) can be at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity, such that the ces undergo homologous recombination. Moreover, a corresponding region of homology between the homology arm and the corresponding target site can be of any length that is sufficient to promote homologous recombination at the cleaved recognition site. For e, a given homology arm and/or corresponding target site can comprise corresponding regions of homology that are from about 400 bp to about 500 bp, from about 500 bp to about 600 bp, from about 600 bp to about 700 bp, from about 700 bp to about 800 bp, from about 800 bp to about 900 bp, or from about 900 bp to about 1000 bp (such as described for the smallTVEC vectors described elsewhere herein); or at least about 5-10, 5-15, 5-20, 5-25, 5-30, 5-35, 5-40, -45, 5- 50, 5-55, 5-60, 5-65, 5- 70, 5-75, 5-80, 5-85, 5-90, 5-95, 5-100, 100-200, or 200-300 kilobases in length or more (such as described in the LTVEC vectors described elsewhere ) such that the homology arm has sufficient homology to undergo homologous recombination with the corresponding target sites within the genome of the cell.

For ease of reference the homology arms are referred to herein an upstream and a downstream homology arm. This terminology relates to the relative on of the homology arms to the insert polynucleotide within the targeting vector.

The homology arms of the targeting vector are therefore designed to pond to a target site with the targeted genomic locus on the Y chromosome or within a nging target locus. Thus, the homology arms can correspond to a c locus that is native to the cell, or alternatively they can correspond to a region of a heterologous or exogenous segment of DNA that was integrated into the Y chromosome, including, but not limited to, transgenes, expression cassettes, or heterologous or ous regions of genomic DNA. Alternatively, the homology arms of the targeting vector can correspond to a region of a yeast artificial chromosome (YAC), a bacterial artificial chromosome (BAC), a human artificial chromosome, or any other engineered c region ned in an appropriate host cell.

Still further the homology arms of the targeting vector can correspond to or be derived from a region of a BAC y, a cosmid y, or a P1 phage library. Thus, in specific embodiments, the gy arms of the targeting vector pond to a genomic locus on the Y chromosome or to a challenging target locus that is native, heterologous or exogenous to a non-human mammal, a rodent, a human, a rat, a mouse, a hamster a rabbit, a pig, a bovine, a deer, a sheep, a goat, a chicken, a cat, a dog, a ferret, a e (e.g., marmoset, rhesus monkey), domesticated mammal or an agricultural mammal, an avian, or any other sm of interest. In further embodiments, the homology arms correspond to a genomic locus of the cell that is not targetable using a conventional method or can be targeted only ectly or only with significantly low efficiency, in the absence of a nick or double-strand break induced by a nuclease agent. In one embodiment, the homology arms are derived from a synthetic DNA.

In still other embodiments, the upstream and downstream gy arms correspond to the same genome as the targeted genome. In one embodiment, the homology arms are from a related , e. g., the targeted genome is a mouse genome of a first strain, and the targeting arms are from a mouse genome of a second strain, wherein the first strain and the second strain are different. In other embodiments, the homology arms are from the genome of the same animal or are from the genome of the same strain, e.g., the targeted genome is a mouse genome of a first strain, and the targeting arms are from a mouse genome from the same mouse or from the same strain.

The targeting vector (such as a large targeting vector) can also comprise a selection cassette or a reporter gene as discussed elsewhere herein. The ion cassette can se a nucleic acid sequence encoding a selection , wherein the nucleic acid sequence is operably linked to a promoter. Such promoters can be an inducible promoter, a promoter that is endogenous to the report gene or the cell, a promoter that is heterologous to the reporter gene or to the cell, a cell-specific promoter, a tissue-specific promoter manner or a developmental stage-specific promoter. In one embodiment, the selection marker is selected from neomycin phosphotransferase (neor), hygromycin B phosphotransferase (hygr), puromycin-N-acetyltransferase (puror), blasticidin S deaminase (bsrr), xanthine/guanine phosphoribosyl transferase (gpt), and herpes simplex virus thymidine kinase (HSV-k), and a combination thereof. The ion marker of the targeting vector can be ﬂanked by the upstream and downstream homology arms or found either 5’ or 3’ to the homology arms.

In one embodiment, the targeting vector (such as a large targeting vector) comprises a reporter gene operably linked to a promoter, wherein the reporter gene encodes a reporter protein ed from the group consisting of LacZ, mPlum, mCherry, thomato, mStrawberry, J-Red, DsRed, e, mKO, mCitrine, Venus, YPet, enhanced yellow ﬂuorescent protein , Emerald, enhanced green ﬂuorescent protein (EGFP), CyPet, cyan ﬂuorescent n (CFP), Cerulean, T-Sapphire, luciferase, alkaline phosphatase, and a combination thereof. Such reporter genes can be ly linked to a er active in the cell. Such promoters can be an inducible promoter, a promoter that is nous to the report gene or the cell, a promoter that is logous to the reporter gene or to the cell, a cell-specific promoter, a tissue-specific promoter manner or a pmental stage-specific promoter.

In one non-limiting ment, the combined use of the targeting vector (including, for example, a large targeting vector) with the nuclease agent results in an increased targeting efficiency compared to the use of the targeting vector alone. In one embodiment, when the targeting vector is used in conjunction with the nuclease agent, targeting efficiency of the targeting vector is increased at least by two-fold, at least three-fold, at least 4-fold, or at least 10-fold when compared to when the ing vector is used alone. iii. Large Targeting Vectors The term “large targeting vector” or “LTVEC” as used herein includes large targeting vectors that comprise homology arms that correspond to and are derived from nucleic acid sequences larger than those typically used by other approaches intended to perform homologous targeting in cells and/or comprising insert polynucleotides comprising nucleic acid sequences larger than those typically used by other approaches intended to perform homologous recombination ing in cells. In specific embodiments, the homology arms and/or the insert polynucleotide of the LTVEC comprises a genomic sequence of a otic cell. The size of the LTVEC is too large to enable screening of targeting events by conventional assays, e. g., southern blotting and long-range (e. g., lkb-5kb) PCR. Examples of the LTVEC, include, but are not limited to, vectors derived from a bacterial artificial chromosome (BAC), a human artificial chromosome or a yeast artificial chromosome (YAC). Non-limiting examples of LTVECs and methods for making them are described, e.g., in US Pat. No. 6,586,251, 6,596,541, 7,105,348, and (PCT/USOl/45375), each of which is herein incorporated by reference.

The LTVEC can be of any length, including, but not limited to, at least about 10kb, about 15kb, about 20kb, about 30kb, about 40kb, about 50kb, about 60kb, about 70kb, about 80kb, about 90kb, about 100kb, about 150kb, about 200kb, from about 10kb to about 15kb, about 15 kb to about 20kb, about 20kb to about 30kb, from about 30kb to about 50kb, from about 50kb to about 300kb, from about 50kb to about 75kb, from about 75kb to about 100kb, from about 100kb to 125kb, from about 125kb to about 150kb, from about 150kb to about 175kb, about 175kb to about 200kb, from about 200kb to about 225kb, from about 225kb to about 250kb, from about 250kb to about 275kb or from about 275kb to about 300kb.

In one embodiment, the LTVEC comprises an insert polynucleotide g from about 5kb to about 200kb, from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 30kb, from about 30kb to about 40kb, from about 40kb to about 50kb, from about 60kb to about 70kb, from about 80kb to about 90kb, from about 90kb to about 100kb, from about 100kb to about 110kb, from about 120kb to about 130kb, from about 130kb to about 140kb, from about 140kb to about 150kb, from about 150kb to about 160kb, from about 160kb to about 170kb, from about 170kb to about 180kb, from about 180kb to about 190kb, or from about 190kb to about 200kb, from about 200kb to about 250kb, from about 250kb to about 300kb, from about 300kb to about 350kb, or from about 350kb to about 400kb.

In other instances, the LTVEC design can be such as to allow for the replacement of a given sequence that is from about 5kb to about 200kb or from about 5kb to about 3.0Mb as described herein. In one ment, the replacement is from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 30kb, from about 30kb to about 40kb, from about 40kb to about 50kb, from about 50kb to about 60kb, from about 60kb to about 70kb, from about 80kb to about 90kb, from about 90kb to about 100kb, from about 100kb to about 110kb, from about 110kb to about 120kb, from about 120kb to about 130kb, from about 130kb to about 140kb, from about 140kb to about 150kb, from about 150kb to about 160kb, from about 160kb to about 170kb, from about 170kb to about 180kb, from about 180kb to about 190kb, from about 190kb to about 200kb, from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 40kb, from about 40kb to about 60kb, from about 60kb to about 80kb, from about 80kb to about 100kb, from about 100kb to about 150kb, or from about 150kb to about 200kb, from about 200kb to about 2015/038001 300kb, from about 300kb to about 400kb, from about 400kb to about 500kb, from about 500kb to about 1Mb, from about 1Mb to about 1.5Mb, from about 1.5Mb to about 2Mb, from about 2Mb to about 2.5Mb, or from about 2.5Mb to about 3Mb.

In one embodiment, the homology arms of the LTVEC are derived from a BAC y, a cosmid library, or a P1 phage library. In other embodiments, the gy arms are derived from the targeted genomic locus of the cell and in some instances the target genomic locus that the LTVEC is designed to target is not targetable using a conventional method. In still other embodiments, the homology arms are derived from a synthetic DNA.

In one embodiment, a sum total of the upstream homology arm and the downstream homology arm in the LTVEC is at least 10kb. In other embodiments, the upstream homology arm ranges from about 5kb to about 100kb. In one embodiment, the downstream homology arm ranges from about 5kb to about 100kb. In other embodiments, the sum total of the upstream and downstream homology arms are from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 30kb, from about 30kb to about 40kb, from about 40kb to about 50kb, from about 50kb to about 60kb, from about 60kb to about 70kb, from about 70kb to about 80kb, from about 80kb to about 90kb, from about 90kb to about 100kb, from about 100kb to about 110kb, from about 110kb to about 120kb, from about 120kb to about 130kb, from about 130kb to about 140kb, from about 140kb to about 150kb, from about 150kb to about 160kb, from about 160kb to about 170kb, from about 170kb to about 180kb, from about 180kb to about 190kb, or from about 190kb to about 200kb. In one embodiment, the size of the deletion is the same or similar to the size of the sum total of the 5' and 3' homology arms of the LTVEC.

In one embodiment, the LTVEC comprises a selection cassette or a er gene as discussed elsewhere herein. iv. Methods ofIntegrating an Insert Polynucleotide Near the Recognition Site on the Y Chromosome by Homologous ination Methods are provided for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell comprising a target c locus on the Y chromosome, (b) introducing into the cell a first targeting vector comprising a first insert polynucleotide ﬂanked by a first and a second homology arm corresponding to a first and a second target site; and (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus on the Y chromosome. Similar s can be performed to target a challenging chromosomal locus. As discussed in detail elsewhere herein, in specific ments, the sum total of the first homology arm and the second homology arm of the targeting vector is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb or at least 10 kb and less than 150 kb. In specific embodiments, an LTVEC is employed.

In other specific embodiments, a smallTVEC is employed. In one non-limiting embodiment, such methods are performed employing the culture media that promotes the development of XY F0 fertile females disclosed herein and thereby generating XY F0 fertile female s.

In other ce, the methods bed herein are employed to produce a ed genetic modification in the Sry gene, as discussed elsewhere herein.

Further provided are methods for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell sing a target genomic locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) ucing into the cell (i) the nuclease agent, wherein the nuclease agent induces a nick or double-strand break at the first recognition site; and, (ii) a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm corresponding to a first and a second target site located in sufficient proximity to the first recognition site; and (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus on the Y chromosome. Similar s can be performed to target a challenging target locus. As discussed in detail elsewhere herein, in specific ments, the sum total of the first homology arm and the second homology arm of the targeting vector is about 0.5 kb, 1 kb, 1.5 kb, 2 kb, 3 kb, 4 kb, 5kb, 6kb, 7kb, 8kb, 9kb, about 0.5 kb to about 1 kb, about 1 kb to about 1.5 kb, about 1.5 kb to about 2 kb, about 2 kb to about 3 kb, about 3 kb to about 4 kb, about 4 kb to about 5kb, about 5kb to about 6 kb, about 6 kb to about 7 kb, about 8 kb to about 9 kb, or is at least 10 kb or at least 10 kb and less than 150 kb. In specific embodiments, an LTVEC is employed. In other specific embodiments, a smallTVEC is ed. In one non-limiting embodiment, such s are med ing the culture media that promotes the development of XY F0 fertile females disclosed herein and thereby generating XY F0 fertile female animals. In other instance, the methods described herein are employed to produce a targeted genetic modification in the Sry gene, as discussed elsewhere herein.

Various methods can also be employed to identify cells having the insert polynucleotide integrated at the genomic target locus. Insertion of the insert polynucleotide at the genomic target locus results in a “modification of ”. The term "modification of allele” or “MOA” includes the modification of the exact DNA sequence of one allele of a gene(s) or chromosomal locus (loci) in a genome. Examples of “modification of allele (MOA)” include, but are not limited to, ons, substitutions, or insertions of as little as a single nucleotide or deletions of many kilobases spanning a gene(s) or chromosomal locus (loci) of interest, as well as any and all possible modifications n these two extremes.

In various embodiments, to facilitate identification of the targeted modification, a high-throughput quantitative assay, namely, modification of allele (MOA) assay, is employed. The MOA assay described herein allows a large-scale screening of a modified allele(s) in a parental chromosome following a genetic cation. The MOA assay can be carried out via various analytical techniques, including, but not limited to, a quantitative PCR, e.g., a real-time PCR (qPCR). For example, the real-time PCR comprises a first primer-probe set that recognizes the target locus and a second primer-probe set that recognizes a rgeted reference locus. In addition, the primer-probe set comprises a ﬂuorescent probe that recognizes the amplified sequence. The quantitative assay can also be carried out via a variety of ical techniques, including, but not limited to, ﬂuorescence- ed in situ hybridization (FISH), comparative genomic hybridization, isothermic DNA amplification, quantitative hybridization to an immobilized probe(s), Invader Probes®, MMP assays®, TaqMan® Molecular Beacon, and EclipseTM probe technology. (See, for example, U82005/0144655, incorporated by reference herein in its entirety).

In various embodiments, in the presence of the nick or double strand bread, targeting ency of a targeting vector (such as a LTVEC or a smallTVEC) at the target genomic locus is at least about 2-fold higher, at least about 3-fold higher, at least about 4-fold higher than in the absence of the nick or double-strand break (using, e. g., the same targeting vector and the same homology arms and corresponding target sites at the c locus of interest but in the absence of an added nuclease agent that makes the nick or double strand break).

The various methods set forth above can be tially repeated to allow for the ed integration of any number of insert polynucleotides into a given targeted genomic locus on the Y chromosome or into a challenging target locus. Thus, the s methods provide for the insertion of at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11, 12,13, 14,15, 16,17, 18, 19, 20 or more insert polynucleotides into the target genomic locus on the Y chromosome or into a nging target locus. In particular embodiments, such sequential tiling methods allow for the reconstruction of large genomic regions from an animal cell or from a WO 00805 mammalian cell (i.e., a human, a man, a rodent, a mouse, a monkey, a rat, a hamster, a icated mammal or an agricultural ) into a targeted genomic locus on a Y chromosome. In such instances, the transfer and reconstruction of genomic regions that include both coding and non-coding regions allow for the complexity of a given region to be preserved by retaining, at least in part, the coding regions, the non-coding s and the copy number variations found within the native c region. Thus, the s methods provide, for example, methods to generate “heterologous” or “exogenous” genomic regions within any mammalian cell or animal of interest. In one non-limiting e, a “humanized” genomic region within a non-human animal is generated.

It is further recognized that along with ing the target genomic locus on the Y chromosome, the s methods and compositions disclosed herein can be employed to also generate at targeted genetic modification on another chromosome. v. Polynucleotides ofInterest Any polynucleotide of interest may be contained in the various insert polynucleotides and thereby integrated at the target genomic locus on the Y chromosome or into a challenging target locus. The methods disclosed herein, e for at least 1, 2, 3, 4, , 6 or more polynucleotides of interest to be integrated into the targeted genomic locus.

The polynucleotide of interest within the insert polynucleotide when integrated at the target genomic locus on the Y chromosome or at a challenging target locus can introduce one or more genetic modifications into the cell. The genetic modification can comprise a deletion of an endogenous nucleic acid sequence and/or the addition of an exogenous or heterologous or orthologous polynucleotide into the target genomic locus. In one embodiment, the genetic modification comprises a replacement of an endogenous nucleic acid sequence with an exogenous polynucleotide of interest at the target genomic locus.

Thus, s provided herein allow for the generation of a genetic modification comprising a knockout, a deletion, an insertion, a replacement (“knock-in”), a point mutation, a domain swap, an exon swap, an intron swap, a regulatory sequence swap, a gene swap, or a combination f in a target genomic locus on the Y chromosome. Such modifications may occur upon integration of the first, second, third, fourth, fifth, six, seventh, or any subsequent insert polynucleotides into the target genomic locus.

The polynucleotide of st within the insert polynucleotide and/or integrated at the target genomic locus can comprise a sequence that is native or homologous to the cell it is introduced into; the polynucleotide of interest can be heterologous to the cell it is introduced to; the polynucleotide of interest can be exogenous to the cell it is introduced into; the polynucleotide of interest can be orthologous to the cell it is introduced into; or the polynucleotide of interest can be from a different species than the cell it is introduced into.

As used herein “homologous” in reference to a sequence is a sequence that is native to the cell. As used herein, “heterologous” in reference to a sequence is a sequence that ates from a foreign s, or, if from the same species, is substantially modified from its native form in ition and/or genomic locus by deliberate human intervention. As used herein, “exogenous” in nce to a sequence is a sequence that originates from a n species.

As used herein, “orthologous” is a polynucleotide from one species that is functionally equivalent to a known reference sequence in another species (i.e., a s variant). The polynucleotide of interest can be from any organism of interest including, but not limited to, non-human, a rodent, a r, a mouse, a rat, a human, a monkey, an avian, an agricultural mammal or a non-agricultural mammal. The cleotide of interest can r comprise a coding region, a non-coding , a tory region, or a genomic DNA. Thus, the 1“, 2nd, 3rd, 4th, 5th, 6th, 7m, and/or any of the subsequent insert polynucleotides can se such sequences.

In one embodiment, the polynucleotide of interest within the insert polynucleotide and/or integrated at the target genomic locus on the Y chromosome is homologous to a mouse nucleic acid sequence, a human nucleic acid, a non-human nucleic acid, a rodent nucleic acid, a rat nucleic acid, a hamster nucleic acid, a monkey nucleic acid, an agricultural mammal nucleic acid, or a non-agricultural mammal nucleic acid. In still further embodiments, the polynucleotide of interest integrated at the target locus is a fragment of a genomic nucleic acid. In one embodiment, the genomic nucleic acid is a mouse genomic nucleic acid, a human genomic nucleic acid, a non-human nucleic acid, a rodent nucleic acid, a rat nucleic acid, a hamster nucleic acid, a monkey c acid, an agricultural mammal nucleic acid or a non-agricultural mammal nucleic acid or a combination f.

In one embodiment, the polynucleotide of interest can range from about 500 nucleotides to about 200kb as described above. The polynucleotide of interest can be from about 500 nucleotides to about 5kb, from about 5kb to about 200kb, from about 5kb to about 10kb, from about 10kb to about 20kb, from about 20kb to about 30kb, from about 30kb to about 40kb, from about 40kb to about 50kb, from about 60kb to about 70kb, from about 80kb to about 90kb, from about 90kb to about 100kb, from about 100kb to about 110kb, from about 120kb to about 130kb, from about 130kb to about 140kb, from about 140kb to about 150kb, from about 150kb to about 160kb, from about 160kb to about 170kb, from about l70kb to about 180kb, from about 180kb to about 190kb, or from about l90kb to about 200kb.

] The polynucleotide of interest within the insert polynucleotide and/or inserted at the target genomic locus on the Y chromosome or into a challenging target locus can encode a polypeptide, can encode an miRNA, can encode a long non-coding RNA, or it can comprise any regulatory regions or non-coding regions of interest including, for example, a regulatory sequence, a er sequence, an enhancer sequence, a riptional repressor-binding sequence, or a deletion of a non-protein-coding sequence, but does not comprise a deletion of a n-coding sequence. In addition, the cleotide of interest within the insert polynucleotide and/or inserted at the target genomic locus on the Y chromosome or at a challenging target locus can encode a protein expressed in the nervous system, the skeletal system, the digestive , the circulatory system, the muscular system, the respiratory system, the cardiovascular , the lymphatic system, the endocrine , the urinary system, the uctive system, or a combination thereof.

The polynucleotide of st within the insert polynucleotide and/or integrated at the target genomic locus on the Y chromosome or at a challenging target locus can comprises a genetic modification in a coding sequence. Such genetic modifications include, but are not limited to, a deletion mutation of a coding sequence or the fusion of two coding sequences.

The polynucleotide of interest within the insert polynucleotide and/or integrated at the target genomic locus on the Y chromosome or at a challenging target locus can comprise a polynucleotide encoding a mutant protein. In one embodiment, the mutant protein is characterized by an altered binding characteristic, d localization, altered expression, and/or altered expression pattern. In one embodiment, the polynucleotide of interest within the insert polynucleotide and/or integrated at the genomic target locus on the Y chromosome or at a challenging target locus ses at least one disease allele. In such instances, the e allele can be a dominant allele or the disease allele is a ive allele. er, the disease allele can comprise a single nucleotide polymorphism (SNP) allele. The polynucleotide of interest encoding the mutant protein can be from any organism, ing, but not limited to, a mammal, a non-human mammal, rodent, mouse, rat, a human, a monkey, an agricultural mammal or a domestic mammal polynucleotide encoding a mutant protein.

The polynucleotide of interest within the insert polynucleotide and/or integrated at the target genomic locus on the Y chromosome or at a challenging target locus can also comprise a regulatory sequence, including for example, a promoter sequence, an enhancer sequence, a transcriptional repressor-binding sequence, or a transcriptional terminator sequence. In specific embodiments, the polynucleotide of interest within the insert polynucleotide and/or integrated at the target genomic locus on the Y chromosome or at a challenging target locus comprises a polynucleotide having a deletion of a non-protein- coding sequence, but does not comprise a deletion of a protein-coding sequence. In one embodiment, the deletion of the non-protein-coding ce comprises a deletion of a regulatory sequence. In another embodiment, the deletion of the regulatory element comprises a deletion of a promoter sequence. In one embodiment, the deletion of the regulatory element comprises a on of an enhancer sequence. Such a polynucleotide of interest can be from any organism, including, but not limited to, a mammal, a non-human mammal, rodent, mouse, rat, a human, a , an agricultural mammal or a domestic mammal polynucleotide encoding a mutant protein.

] The various methods disclosed herein can be employed to te a variety of cations in a challenging genomic locus or in the Y chromosome locus (such as Sry).

Such modifications include, for example, a replacement of an nous nucleic acid sequence with a gous or an orthologous nucleic acid sequence; a deletion of an endogenous nucleic acid sequence; a deletion of an endogenous nucleic acid sequence, wherein the deletion ranges from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 600 kb, from about 600 kb to about 700 kb, from about 700 kb to about 800 kb, from about 800 kb to about 900 kb, from about 900 kb to about 1 Mb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb; an ion of an exogenous nucleic acid ce; an insertion of an exogenous c acid sequence ranging from about 5kb to about 10kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, from about 150 kb to about 200 kb, from about 200 kb to about 250 kb, from about 250 kb to about 300 kb, from about 300 kb to about 350 kb, or from about 350 kb to about 400 kb; an insertion of an exogenous nucleic acid sequence comprising a homologous or an orthologous nucleic acid sequence; an insertion of a ic nucleic acid sequence comprising a human and a non-human nucleic acid sequence; an insertion of a conditional allele flanked with site- specific recombinase target sequences; an insertion of a selectable marker or a reporter gene operably linked to a third promoter active in the mammalian cell; or a combination thereof.

III. Methods ofIntroducing Sequences and Generation of Transgenic Animals As outlined above, methods and compositions are provided herein to allow for the targeted genetic modification of one or more polynucleotides of interest located on the Y chromosome, at a challenging target locus, or a decrease in the level and/or activity of the Sry protein. It is r recognized that in addition to a targeted genetic modification to a sequence on the Y chromosome or on a challenging target chromosomal locus, additional targeted genetic modification can be made on other chromosomes. Such systems that allow for these targeted genetic cations can employ a variety of components and for ease of reference, herein the term “targeted genomic integration system” generically includes all the components required for an integration event (i.e. the various nuclease agents, recognition sites, insert DNA polynucleotides, targeting vectors, target genomic locus, and polynucleotides of interest).

The methods provided herein comprise introducing into a cell one or more polynucleotides or polypeptide constructs comprising the various components of the targeted genomic ation . "Introducing" means presenting to the cell the ce eptide or polynucleotide) in such a manner that the sequence gains access to the interior of the cell. The s provided herein do not depend on a ular method for introducing any component of the targeted c integration system into the cell, only that the polynucleotide gains access to the interior of a least one cell. Methods for introducing polynucleotides into various cell types are known in the art and include, but are not limited to, stable ection methods, transient transfection methods, and virus-mediated s.

In some embodiments, the cells employed in the methods and compositions have a DNA construct stably orated into their genome. "Stably incorporated" or "stably introduced" means the introduction of a polynucleotide into the cell such that the nucleotide sequence integrates into the genome of the cell and is capable of being inherited by y thereof. Any protocol may be used for the stable incorporation of the DNA constructs or the various components of the targeted genomic ation system.

Transfection protocols as well as protocols for introducing ptides or polynucleotide sequences into cells may vary. miting transfection methods include chemical-based transfection methods include the use of liposomes; nanoparticles; calcium ate (Graham et al. (1973). Virology 52 (2): 456—67, Bacchetti et al. (1977) Proc Natl Acad Sci USA 74 (4): 1590—4 and, Kriegler, M (1991). Transfer and Expression: A Laboratory Manual. New York: W. H. Freeman and Company. pp. 96—97); dendrimers; or cationic polymers such as extran or polyethylenimine. Non chemical methods include electroporation; Sono-poration; and optical transfection . Particle-based transfection include the use of a gene gun, magnet assisted transfection ( m, J. (2006) Current Pharmaceutical hnology 7, 277—28). Viral methods can also be used for transfection.

In one embodiment, the nuclease agent is introduced into the cell simultaneously with the targeting vector, the smallTVEC, or the large targeting vector (LTVEC).

Alternatively, the nuclease agent is introduced separately from the targeting vector, smallTVEC, or the LTVEC over a period of time. In one embodiment, the nuclease agent is introduced prior to the uction of the targeting , smallTVEC, or the LTVEC, while in other embodiments, the nuclease agent is introduced following introduction of the targeting vector, smallTVEC, or the LTVEC.

Non-human animals can be generated employing the various methods disclosed herein. Such methods comprises (1) integrating one or more polynucleotide of interest at the target c locus of the Y chromosome of a pluripotent cell of the non-human animal to generate a genetically modified pluripotent cell comprising the insert polynucleotide in the targeted genomic locus of the Y chromosome employing the methods disclosed herein; (2) selecting the genetically modified pluripotent cell having the one or more polynucleotides of interest at the target genomic locus of the Y chromosome; (3) introducing the genetically modified pluripotent cell into a host embryo of the non-human animal at a pre-morula stage; and (4) implanting the host embryo comprising the genetically modified pluripotent cell into a surrogate mother to te an F0 generation derived from the genetically modified pluripotent cell. Similar methods can be employed to target a challenging target chromosomal locus. The non-human animal can be a man , a , a mouse, a rat, a hamster, a monkey, an ltural mammal or a domestic mammal, or a fish or a bird.

The pluripotent cell can be a human ES cell, a non-human ES cell, a rodent ES cell, a mouse ES cell, a rat ES cell, a hamster ES cell, a monkey ES cell, an agricultural mammal ES cell or a icated mammal ES cell. In other embodiments, the pluripotent cell is a mammalian cell, human cell, a non-human mammalian cell, a human pluripotent cell, a human ES cell, a human adult stem cell, a developmentally-restricted human progenitor cell, a human iPS cell, a human cell, a rodent cell, a rat cell, a mouse cell, a hamster cell. In one embodiment, the targeted genetic cation decreases the level and/or activity of the 2015/038001 Sry protein. In such instances, the pluripotent cell can comprise an XY ES cell or an XY iPS cell. Methods of culturing such cells to e the development of F0 fertile XY female animals are described in detail elsewhere herein.

Nuclear transfer ques can also be used to generate the man mammalian animals. Brieﬂy, methods for nuclear er include the steps of: (l) enucleating an oocyte; (2) isolating a donor cell or nucleus to be combined with the enucleated oocyte; (3) inserting the cell or nucleus into the ated oocyte to form a reconstituted cell; (4) implanting the reconstituted cell into the womb of an animal to form an embryo; and (5) allowing the embryo to develop. In such methods oocytes are generally retrieved from deceased animals, although they may be isolated also from either oviducts and/or ovaries of live animals. s can be d in a variety of medium known to those of ry skill in the art prior to ation. Enucleation of the oocyte can be performed in a number of manners well known to those of ordinary skill in the art. Insertion of the donor cell or nucleus into the enucleated oocyte to form a reconstituted cell is usually by microinjection of a donor cell under the zona pellucida prior to fusion. Fusion may be induced by application of a DC electrical pulse across the contact/fusion plane rofusion), by exposure of the cells to fusion-promoting chemicals, such as polyethylene glycol, or by way of an inactivated virus, such as the Sendai virus. A reconstituted cell is typically activated by electrical and/or non-electrical means before, during, and/or after fusion of the nuclear donor and recipient . Activation s include electric pulses, chemically induced shock, penetration by sperm, increasing levels of divalent cations in the oocyte, and reducing phosphorylation of cellular proteins (as by way of kinase inhibitors) in the oocyte. The activated reconstituted cells, or embryos, are typically cultured in medium well known to those of ordinary skill in the art and then transferred to the womb of an animal.

See, for example, US20080092249, WO/l999/005266A2, US20040177390, WO/2008/017234Al, and US Patent No. 7,612,250, each of which is herein incorporated by reference.

Other methods for making a non-human animal comprising in its ne one or more genetic modifications as described herein is provided, comprising: (a) modifying a targeted genomic locus on the Y chromosome of a non-human animal in a prokaryotic cell employing the various methods described herein; (b) selecting a modified prokaryotic cell comprising the genetic modification at the targeted c locus; (c) isolating the genetically modified targeting vector from the genome of the modified prokaryotic cell; (d) introducing the cally modified targeting vector into a pluripotent cell of the non-human WO 00805 animal to generate a genetically modified pluripotent cell comprising the insert nucleic acid at the targeted genomic locus of the Y chromosome; (e) ing the genetically modified pluripotent cell; (f) introducing the genetically modified pluripotent cell into a host embryo of the non-human animal at a pre-morula stage; and (g) implanting the host embryo sing the genetically modified pluripotent cell into a surrogate mother to generate an F0 generation derived from the genetically modified pluripotent cell. In such s the targeting vector can comprise a large targeting vector or a smallTVEC. Similar s can be employed to target a challenging target locus. The non-human animal can be a non-human mammal, a rodent, a mouse, a rat, a hamster, a monkey, an agricultural mammal or a domestic .

The pluripotent cell can be a human ES cell, a non-human ES cell, a rodent ES cell, a mouse ES cell, a rat ES cell, a hamster ES cell, a monkey ES cell, an agricultural mammal ES cell or a domestic mammal ES cell. In other embodiments, the pluripotent cell is a ian cell, human cell, a non-human mammalian cell, a human pluripotent cell, a human ES cell, a human adult stem cell, a developmentally-restricted human progenitor cell, a human iPS cell, a human cell, a rodent cell, a rat cell, a mouse cell, a hamster cell. In one embodiment, the ed genetic modification ses the level and/or activity of the Sry protein. In such instances, the pluripotent cell can comprise an XY ES cell or an XY iPS cell. Methods of culturing such cells to promote the development of F0 fertile XY female animals are described in detail ere herein.

In further methods, the isolating step (c) r comprises (cl) linearizing the genetically modified targeting vector (i.e., the genetically ed LTVEC). In still r embodiments, the introducing step (d) further comprises (dl) introducing a nuclease agent as described herein into the pluripotent cell. In one embodiment, selecting steps (b) and/or (e) are carried out by applying a selectable agent as described herein to the prokaryotic cell or the pluripotent cell. In one embodiment, selecting steps (b) and/or (e) are carried out via a modification of allele (MOA) assay as described herein.

Further methods for modifying a target genomic locus of an animal cell via bacterial gous recombination (BHR) in a prokaryotic cell are provided and comprise: (a) providing a prokaryotic cell comprising a target genomic locus of the Y chromosome; (b) introducing into the prokaryotic cell a targeting vector (as described above) comprising an insert cleotide ﬂanked with a first upstream homology arm and a first downstream homology arm, wherein the insert cleotide comprises a mammalian genomic region, and introducing into the prokaryotic cell a nuclease agent that makes a nick or double-strand break at or near the first recognition site, and (c) selecting a targeted prokaryotic cell comprising the insert polynucleotide at the target genomic locus of the chromosome, wherein the prokaryotic cell is capable of sing a recombinase that mediates the BHR. Similar methods can be employed to target a challenging target locus. Steps (a)-(c) can be serially repeated as sed herein to allow the introduction of multiple insert polynucleotides at the targeted genomic locus in the prokaryotic cell. Once the targeted genomic locus is “built” with the prokaryotic cell, a targeting vector comprising the modified target genomic locus of the Y chromosome can be isolated from the yotic cell and introduced into a target genomic locus of the Y chromosome within a mammalian cell. Mammalian cells comprising the modified genomic locus of the Y chromosome can then be made into non-human transgenic animals.

Further methods for modifying a target genomic locus of an animal cell via bacterial homologous recombination (BHR) in a prokaryotic cell are provided and comprise: (a) providing a prokaryotic cell comprising a target c locus of the Y chromosome; (b) introducing into the prokaryotic cell a targeting vector (as described above) comprising an insert polynucleotide flanked with a first am homology arm and a first downstream homology arm, wherein the insert polynucleotide comprises a ian genomic region, and (c) selecting a targeted prokaryotic cell comprising the insert polynucleotide at the target genomic locus of the chromosome, wherein the prokaryotic cell is e of expressing a recombinase that mediates the BHR. Similar s can be ed to target a challenging target locus. Steps (a)-(c) can be serially repeated as disclosed herein to allow the introduction of multiple insert polynucleotides at the targeted genomic locus in the prokaryotic cell. Once the targeted genomic locus is “built” with the prokaryotic cell, a targeting vector comprising the ed target genomic locus of the Y some can be isolated from the prokaryotic cell and introduced into a target c locus of the Y chromosome within a mammalian cell. Mammalian cells comprising the modified genomic locus of the Y chromosome can then be made into non-human transgenic animals In some embodiments, various genetic modifications of the target genomic loci described herein can be carried out by a series of homologous recombination reactions (BHR) in bacterial cells using an LTVEC d from Bacterial Artificial some (BAC) DNA using VELOCIGENE® c engineering technology (see, e.g., US Pat. No. 6,586,251 and Valenzuela, D. M. et a1. (2003), High-throughput engineering of the mouse genome coupled with high-resolution expression analysis, Nature hnology 21(6): 652- 659, which is incorporated herein by reference in their entireties).

] In some embodiments, targeted XY pluripotent and/or totipotent cells (i.e., X YES cells or XY iPS cells) comprising various genetic cations as described herein are used as insert donor cells and introduced into a pre-morula stage embryo from a corresponding organism, e. g., an 8-cell stage mouse embryo, via the VELOCIMOUSE® method (see, e. g., US 7,576,259, US 7,659,442, US 7,294,754, and US 2008-0078000 Al, all of which are incorporated by reference herein in their entireties). The non-human animal embryo comprising the genetically modified XY pluripotent and/or totipotent cells (i.e., XY ES cells or XY iPS cells) is ted until the blastocyst stage and then implanted into a surrogate mother to e an F0 generation. In some embodiments, targeted mammalian ES cells comprising s c cations as described herein are introduced into a blastocyst stage embryo. Non-human animals bearing the cally modified genomic locus of the Y chromosome can be identified via modification of allele (MOA) assay as described herein.

The resulting F0 generation non-human animal derived from the cally modified XY pluripotent and/or totipotent cells (i.e., X YES cells or XY iPS cells) is crossed to a wild-type non-human animal to obtain F1 generation offspring. Following genotyping with specific primers and/or probes, Fl non-human animals that are heterozygous for the genetically modified c locus are crossed to each other to produce F2 generation non-human animal offspring that are homozygous for the genetically modified c locus of the Y chromosome or for the genetically ed challenging target locus.

IV. Cells and Expression Cassettes The various methods described herein employ a genomic locus targeting system for the Y chromosome or for a challenging target locus in a cell. Such cells include prokaryotic cells such as bacterial cells including E. coli, or eukaryotic cells such as yeast, insect, amphibian, plant, or mammalian cells, including, but not limited to a mouse cell, a rat cell, a rabbit cell, a pig cell, a bovine cell, a deer cell, a sheep cell, a goat cell, a chicken cell, a cat cell, a dog cell, a ferret cell, a primate (e. g., et, rhesus monkey) cell, and the like and cells from domesticated mammals or cells from agricultural mammals. Some cells are non-human, particularly non-human mammalian cells. In some embodiments, for those mammals for which suitable genetically modifiable pluripotent cells are not readily available, other methods are employed to reprogram somatic cells into pluripotent cells, e. g., via uction into somatic cells of a combination of pluripotency-inducing factors, including, but not limited to, Oct3/4, Sox2, KLF4, Myc, Nanog, LIN28, and Glisl. In such methods, the cell can also be a mammalian cell, human cell, a non-human mammalian cell, a non- human cell, a cell from a rodent, a rat, a mouse, a hamster, a fibroblast cell or any other host cell. In other ments, the cell is a pluripotent cell, an induced pluripotent stem (iPS) cell, a non-human embryonic stem (ES) cell. Such cells include pluripotent cells, including, for example, induced pluripotent stem (iPS) cells, mouse embryonic stem (ES) cells, rat embryonic stem (ES) cells, human nic (ES) cells, or pmentally restricted human progenitor cells, a rodent embryonic stem (ES) cell, a mouse embryonic stem (ES) cell or a rat embryonic stem (ES) cell.

The terms “polynucleotide,” “polynucleotide sequence,77 (Cnucleic acid sequence,” and “nucleic acid fragment” are used interchangeably herein. These terms encompass nucleotide sequences and the like. A polynucleotide may be a polymer of RNA or DNA that is single- or double-stranded, that optionally contains synthetic, non-natural or altered nucleotide bases. A polynucleotide in the form of a polymer of DNA may be comprised of one or more segments of cDNA, genomic DNA, synthetic DNA, or mixtures thereof.

Polynucleotides can comprise ibonucleotides and ribonucleotides include both naturally occurring molecules and synthetic analogues, and any combination these. The polynucleotides provided herein also encompass all forms of sequences including, but not limited to, single-stranded forms, double-stranded forms, hairpins, nd-loop ures, and the like.

] Further provided are inant polynucleotides. The terms “recombinant polynucleotide” and “recombinant DNA construct” are used interchangeably herein. A recombinant construct comprises an artificial or heterologous combination of c acid sequences, e. g., regulatory and coding sequences that are not found together in nature. In other embodiments, a recombinant construct may comprise regulatory sequences and coding sequences that are derived from different s, or regulatory sequences and coding sequences derived from the same source, but arranged in a manner different than that found in nature. Such a construct may be used by itself or may be used in conjunction with a vector. If a vector is used, then the choice of vector is ent upon the method that is used to transform the host cells as is well known to those skilled in the art. For example, a plasmid vector can be used. Screening may be accomplished by Southern is of DNA, Northern analysis of mRNA expression, blotting analysis of n expression, or phenotypic analysis, among .

In specific embodiments, one or more of the components described herein can be provided in an expression cassette for expression in the pluripotent and/or totipotent cell.

The cassette can include 5' and 3' regulatory sequences operably linked to a polynucleotide provided . “Operably linked” means a functional linkage between two or more elements. For example, an operable linkage between a polynucleotide of interest and a tory sequence (i.e., a promoter) is a functional link that allows for expression of the polynucleotide of interest. Operably linked elements may be uous or non-contiguous.

When used to refer to the joining of two protein coding regions, operably linked means that the coding regions are in the same reading frame. In another instance, a nucleic acid sequence encoding a protein may be operably linked to regulatory sequences (e. g., promoter, enhancer, silencer sequence, etc.) so as to retain proper transcriptional regulation. The cassette may additionally contain at least one additional polynucleotide of interest to be co-introduced into the ES cell. Alternatively, the additional polynucleotide of interest can be provided on multiple expression cassettes. Such an expression cassette is provided with a plurality of restriction sites and/or recombination sites for insertion of a recombinant polynucleotide to be under the transcriptional regulation of the regulatory regions. The expression cassette may additionally contain selection marker genes.

The expression cassette can e in the 5'-3' direction of ription, a transcriptional and ational initiation region (i.e., a er), a recombinant polynucleotide provided herein, and a transcriptional and translational termination region (i.e., termination region) functional in mammalian cell or a host cell of interest. The regulatory regions (i.e., promoters, transcriptional regulatory regions, and transcriptional and translational termination regions) and/or a polynucleotide ed herein may be native/analogous to the host cell or to each other. Alternatively, the regulatory regions and/or a polynucleotide provided herein may be heterologous to the host cell or to each other. For example, a er operably linked to a heterologous polynucleotide is from a species different from the species from which the polynucleotide was d, or, if from the same/analogous species, one or both are substantially modified from their original form and/or genomic locus, or the promoter is not the native promoter for the operably linked cleotide. Alternatively, the regulatory s and/or a recombinant polynucleotide provided herein may be entirely synthetic.

The ation region may be native with the transcriptional initiation region, may be native with the operably linked recombinant polynucleotide, may be native with the host cell, or may be derived from r source (i.e., foreign or heterologous) to the er, the recombinant polynucleotide, the host cell, or any combination thereof.

In preparing the expression cassette, the various DNA fragments may be manipulated, so as to provide for the DNA ces in the proper orientation. Toward this end, adapters or linkers may be employed to join the DNA fragments or other manipulations may be ed to e for convenient restriction sites, removal of superﬂuous DNA, removal of restriction sites, or the like. For this purpose, in vitro mutagenesis, primer repair, restriction, annealing, resubstitutions, e. g., transitions and transversions, may be involved.

A number of promoters can be used in the expression cassettes provided herein.

The promoters can be selected based on the desired outcome. It is recognized that different applications can be enhanced by the use of different promoters in the expression cassettes to modulate the , location and/or level of expression of the polynucleotide of interest.

Such expression constructs may also contain, if desired, a promoter regulatory region (e. g., one conferring inducible, constitutive, environmentally- or developmentally-regulated, or cell- or tissue-specific/selective expression), a transcription initiation start site, a me binding site, an RNA sing signal, a transcription ation site, and/or a polyadenylation signal.

Non-limiting embodiments include: 1. An in vitro culture comprising (a) a non-human mammalian XY embryonic stem (ES) cell having a modification that ses the level and/or activity of an Sry protein; and, (b) a medium sing a base medium and ments suitable for maintaining the non-human mammalian ES cell in culture, wherein the medium ts one or more of the following teristic: an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg; a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50 mM to about 110 mM; a carbonic acid salt concentration of about l7mM to about 30 mM; a total alkaline metal halide salt and carbonic acid salt concentration of about 85mM to about 130 mM; and/or a combination of any two or more thereof. 2. The in vitro culture of claim 1, wherein the non-human mammalian XY ES cell is from a rodent. 3. The in vitro e of claim 2, wherein the rodent is a mouse. 4. The in vitro culture of embodiment 3, wherein the mouse XY ES cell is a VGFl mouse ES cell.

. The in vitro culture of embodiment 2, wherein the rodent is a rat or a hamster. 6. The in vitro e of any one of embodiments 1-5, wherein the decreased level and/or activity of the Sry protein is from a genetic modification in the Sry gene. 7. The in vitro culture of embodiment 6, wherein the genetic modification in the Sry gene comprises an insertion of one or more nucleotides, a on of one or more nucleotides, a substitution of one or more nucleotides, a knockout, a knockin, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence or a combination thereof. 8. The in vitro e of any one of embodiments 1-7, wherein the non-human mammalian ES cell comprises one, two, three or more targeted genetic modifications. 9. The in vitro culture of embodiment 8, wherein the targeted genetic modification comprises an insertion, a deletion, a knockout, a knockin, a point mutation, or a combination thereof.

. The in vitro culture of embodiment 8, wherein the targeted genetic modification comprises at least one insertion of a heterologous polynucleotide into the genome of the XY ES cell. 11. The in vitro culture of any one of ments 8-10, wherein the targeted genetic modification is on an me. 12. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits 50 i 5 mM NaCl, 26 i 5 mM carbonate, and 218 i 22 mOsm/kg. 13. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits about 3 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 218 mOsm/kg. 14. The in vitro culture of any one of embodiments 1-11, wherein the base medium ts 87 i 5 mM NaCl, 18 i 5 mM carbonate, and 261 i 26 mOsm/kg.

. The in vitro e of any one of ments 1-11, wherein the base medium exhibits about 5.1 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 261 g. 16. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits 110 i 5 mM NaCl, 18 i 5 mM carbonate, and 294 i 29 g. 17. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits about 6.4 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 294 mOsm/kg. 18. The in vitro culture of any one of ments 1-11, wherein the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, and 270 i 27 mOsm/kg. 19. The in vitro culture of any one of embodiments 1-11, n the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 270 mOsm/kg.

. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, 86 i 5 mM glucose, and 322 i 32 mOsm/kg. 21. The in vitro culture of any one of embodiments 1-11, wherein the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium onate, 15.5 mg/mL glucose, and 322 mOsm/kg. 22. The in vitro culture of any one of ments 1-21, wherein upon introduction of the non-human mammalian XY ES cells into a host embryo and following gestation of the host embryo, at least 80% of the F0 non-human mammals are XY females which upon attaining sexual maturity the F0 XY female non-human mammal is fertile. 23. A method for making a fertile female XY non-human mammal in an F0 generation, sing: (a) ing a donor non-human mammalian XY embryonic stem (ES) cell having a modification that decreases the level and/or activity of an Sry protein in a medium comprising a base medium and supplements suitable for maintaining the non-human mammalian ES cell in culture, wherein the medium exhibits a characteristic comprising one or more of the following: an osmolality from about 200 mOsm/kg to less than about 329 mOsm/kg; a conductivity of about 11 mS/cm to about 13 mS/cm; a salt of an alkaline metal and a halide in a concentration of about 50mM to about 110 mM; a carbonic acid salt concentration of about 17 mM to about 30 mM; a total ne metal halide salt and carbonic acid salt concentration of about 85 mM to about 130 mM; and/or a combination of any two or more thereof; (b) introducing the donor XY non-human mammalian ES cell into a host ; (c) gestating the host embryo; and, (d) obtaining an F0 XY female man mammal, wherein upon attaining sexual maturity the F0 XY female non-human mammal is fertile. 24. The method of embodiment 23, wherein the non-human mammalian XY ES cell is from a rodent.

. The method of embodiment 24, wherein the rodent is a mouse. 26. The method of embodiment 25, wherein the mouse XY ES cell is a VGFl mouse ES cell. 27. The method of embodiment 24, wherein the rodent is a rat or a hamster. 28. The method of any one of embodiments 23-27, wherein the sed level and/or activity of the Sry protein is from a genetic modification in the Sry gene. 29. The method of embodiment 28, wherein the genetic modification in the Sry gene comprises an insertion of one or more nucleotides, a deletion of one or more tides, a substitution of one or more nucleotides, a knockout, a knockin, a replacement of an endogenous nucleic acid sequence with a heterologous nucleic acid sequence or a ation thereof.

. The method of any one of embodiments 23-29, wherein the non-human mammalian ES cell comprises one, two, three or more targeted genetic modifications. 31. The method of embodiment 30, wherein the targeted genetic modification comprises an insertion, a deletion, a ut, a knockin, a point mutation, or a combination thereof. 32. The method of embodiment 30, n the targeted genetic modification comprises at least one insertion of a heterologous polynucleotide into a genome of the XY ES cell. 33. The method of any one of embodiments 30-32, wherein the targeted genetic modification is on an autosome. 34. The method of any one of embodiments 23-33, wherein the base medium ts 50 i 5 mM NaCl, 26 i 5 mM carbonate, and 218 i 22 mOsm/kg.

. The method of any one of embodiments 23-33, wherein the base medium exhibits about 3 mg/mL NaCl, 2.2 mg/mL sodium onate, and 218 mOsm/kg. 36. The method of any one of embodiments 23-33, wherein the base medium exhibits 87 i 5 mM NaCl, 18 i 5 mM carbonate, and 261 i 26 mOsm/kg. 37. The method of any one of embodiments 23-33, wherein the base medium exhibits about 5.1 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 261 mOsm/kg. 38. The method of any one of embodiments 23-33, wherein the base medium exhibits 110 i 5 mM NaCl, 18 i 5 mM carbonate, and 294 i 29 mOsm/kg. 39. The method of any one of ments 23-33, wherein the base medium exhibits about 6.4 mg/mL NaCl, 1.5 mg/mL sodium bicarbonate, and 294 mOsm/kg. 40. The method of any one of embodiments 23-33, wherein the base medium ts 87 i 5 mM NaCl, 26 i 5 mM carbonate, and 270 i 27 mOsm/kg. 41. The method of any one of embodiments 23-33, wherein the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, and 270 mOsm/kg. 42. The method of any one of ments 23-33, wherein the base medium exhibits 87 i 5 mM NaCl, 26 i 5 mM carbonate, 86 i 5 mM glucose, and 322 i 32 mOsm/kg. 43. The method of any one of embodiments 23-33, wherein the base medium exhibits about 5.1 mg/mL NaCl, 2.2 mg/mL sodium bicarbonate, 15.5 mg/mL glucose, and 322 mOsm/kg. 44. A method of producing a transgenic non-human mammal homozygous for a targeted genetic mutation in the F1 generation comprising: (a) crossing an F0 XY fertile female having a decreased level and/or ty of the Sry protein with a cohort clonal sibling, derived from the same ES cell clone, F0 XY male non-human mammal, wherein the F0 XY fertile female man mammal and the F0 XY male non-human mammal each is heterozygous for the genetic mutation; and, (b) obtaining an F1 progeny mouse that is homozygous for the c modification. 45. A method for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell comprising a target genomic locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) introducing into the cell (i) the nuclease agent, wherein the nuclease agent induces a nick or -strand break at the first recognition site; and, (ii) a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm corresponding to a first and a second target site located in sufficient proximity to the first recognition site, n a sum total of the first homology arm and the second homology arm is at least 4kb but less than 150kb; and, (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus. 46. A method for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell sing a target genomic locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) introducing into the cell a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm ponding to a first and a second target site, wherein a sum total of the first homology arm and the second homology arm is at least 4kb but less than 150kb; and, (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target c locus. 47. The method of embodiment 45 or 46, wherein the cell is a mammalian cell. 48. The method of embodiment 47, wherein the ian cell is a non-human cell. 49. The method of embodiment 47, wherein the mammalian cell is from a rodent. 50. The method of embodiment 49, wherein the rodent is a rat, a mouse or a hamster. 51. The method of any one of ments 45-50, wherein the cell is a pluripotent cell. 52. The method of any one of embodiments 45-50, wherein the mammalian cell is an induced pluripotent stem (iPS) cell. 53. The method of ment 51, wherein the pluripotent cell is a non-human embryonic stem (ES) cell. 54. The method of embodiment 51, wherein the pluripotent cell is a rodent embryonic stem (ES) cell, a mouse embryonic stem (ES) cell or a rat embryonic stem (ES) cell. 55. The method of any one of embodiments 45 and 47-54, wherein the nuclease agent is an mRNA encoding a nuclease. 56. The method of any one of ments 45 and 47-54, wherein the nuclease agent is a zinc finger nuclease (ZFN). 57. The method of any one of embodiments 45 and 47-54, wherein the nuclease agent is a Transcription Activator-Like Effector se ). 58. The method of any one of embodiments 45 and 47-54, wherein the nuclease agent is a meganuclease. 59. The method any one of ments 45 and 47-54, wherein the nuclease agent is a CRISPR RNA guided Cas9 endonuclease. 60. A method for modifying the Y chromosome comprising exposing the Y chromosome to a Cas n and a CRISPR RNA in the presence of a large targeting vector (LTVEC) comprising a nucleic acid sequence of at least 10 kb, wherein following exposure to the Cas protein, the CRISPR RNA, and the LTVEC, the Y chromosome is modified to contain at least 10 kb nucleic acid sequence. 61. The method of embodiment 60, wherein the LTVEC comprises a nucleic acid sequence of at least 20 kb, at least 30 kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, or at least 90 kb. 62. The method of embodiment 60, wherein the LTVEC ses a nucleic acid sequence of at least 100 kb, at least 150 kb, or at least 200 kb. 63. A method for modifying a target genomic locus on the Y chromosome, comprising: (a) ing a mammalian cell comprising the target genomic locus on the Y chromosome, wherein the target genomic locus comprises a guide RNA (gRNA) target sequence; (b) introducing into the ian cell: (i) a large targeting vector (LTVEC) comprising a first nucleic acid flanked with targeting arms homologous to the target genomic locus, wherein the LTVEC is at least 10 kb; (ii) a first expression construct comprising a first promoter operably linked to a second nucleic acid encoding a Cas protein, and (iii) a second sion uct comprising a second promoter operably linked to a third nucleic acid encoding a guide RNA (gRNA) comprising a nucleotide ce that hybridizes to the gRNA target sequence and a trans-activating CRISPR RNA (trachNA), wherein the first and the second promoters are active in the mammalian cell; and (c) identifying a modified mammalian cell comprising a targeted genetic modification at the target genomic locus on the Y some. 64. The method of embodiment 63, wherein the LTVEC is at least 15 kb, at least kb, at least 30kb, at least 40 kb, at least 50 kb, at least 60 kb, at least 70 kb, at least 80 kb, or at least 90 kb. 65. The method of embodiment 63, wherein the LTVEC is at least 100 kb, at least 150 kb, or at least 200 kb. 66. The method of ment 63, wherein the mammalian cell is a non-human mammalian cell. 67. The method of embodiment 63, n the mammalian cell is a fibroblast cell. 68. The method of embodiment 63, wherein the mammalian cell is from a rodent. 69. The method of embodiment 68, n the rodent is a rat, a mouse, or a hamster. 70. The method of embodiment 63, wherein the mammalian cell is a pluripotent cell. 71. The method of embodiment 70, wherein the pluripotent cell is an induced pluripotent stem (iPS) cell. 72. The method of embodiment 70, wherein the pluripotent cell is a mouse embryonic stem (ES) cell or a rat embryonic stem (ES) cell. 73. The method of embodiment 70, wherein the pluripotent cell is a developmentally restricted human itor cell. 74. The method of embodiment 63, wherein the Cas protein is a Cas9 protein. 75. The method of embodiment 74, wherein the gRNA target sequence is immediately ﬂanked by a Protospacer Adjacent Motif (PAM) sequence. 76. The method of ment 63, wherein the sum total of 5’ and 3’ homology arms of the LTVEC is from about 10 kb to about 150 kb. 77. The method of embodiment 76, wherein the sum total of the 5’ and the 3’ homology arms of the LTVEC is from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 120 kb, or from about 120 kb to 150 kb. 78. The method of embodiment 63, wherein the targeted genetic modification comprises: (a) a replacement of an endogenous nucleic acid sequence with a homologous or an ogous nucleic acid ce; (b) a deletion of an endogenous nucleic acid sequence; (c) a deletion of an endogenous nucleic acid sequence, wherein the deletion ranges from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, or from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb; (d) insertion of an exogenous nucleic acid sequence; (e) insertion of an exogenous nucleic acid sequence ranging from about 5kb to about 10kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, from about 150 kb to about 200 kb, from about 200 kb to about 250 kb, from about 250 kb to about 300 kb, from about 300 kb to about 350 kb, or from about 350 kb to about 400 kb; (f) ion of an ous nucleic acid sequence comprising a gous or an orthologous nucleic acid sequence; (g) insertion of a ic nucleic acid sequence comprising a human and a man nucleic acid sequence; (h) insertion of a conditional allele ﬂanked with site-specific recombinase target sequences; (i) insertion of a selectable marker or a reporter gene operably linked to a third promoter active in the mammalian cell; or (1') a combination f. 79. The method of embodiment 63, wherein the target genomic locus comprises (i) a 5’ target sequence that is homologous to a 5’ homology arm; and (ii) a 3’ target sequence that is homologous to a 3’ homology arm. 80. The method of embodiment 79, wherein the 5’ target sequence and the 3’ target sequence is separated by at least 5 kb but less than 3 Mb. 81. The method of embodiment 79, wherein the 5’ target sequence and the 3’ target sequence is separated by at least 5 kb but less than 10 kb, at least 10 kb but less than 20 kb, at least 20 kb but less than 40 kb, at least 40 kb but less than 60 kb, at least 60 kb but less than 80 kb, at least about 80 kb but less than 100 kb, at least 100 kb but less than 150 kb, or at least 150 kb but less than 200 kb, at least about 200 kb but less than about 300 kb, at least about 300 kb but less than about 400 kb, at least about 400 kb but less than about 500 kb, at least about 500 kb but less than about le, at least about 1 Mb but less than about 1.5 Mb, at least about 1.5 Mb but less than about 2 Mb, at least about 2 Mb but less than about 2.5 Mb, or at least about 2.5 Mb but less than about 3 Mb. 82. The method of embodiment 63, wherein the first and the second expression constructs are on a single nucleic acid molecule. 83. The method of embodiment 63, wherein the target genomic locus comprises the Sry locus. 84. A method for targeted genetic modification on the Y chromosome of a non- human animal, comprising: (a) modifying a genomic locus of interest on the Y chromosome of a non-human pluripotent cell according to the method of embodiment 4, thereby producing a genetically ed non-human pluripotent cell comprising a targeted genetic modification on the Y chromosome; (b) introducing the modified non-human otent cell of (a) into a non-human host embryo; and (c) gestating the non-human host embryo comprising the modified pluripotent cell in a surrogate , wherein the surrogate mother produces F0 progeny comprising the targeted genetic cation, wherein the targeted genetic modification is capable of being itted h the germline. 85. The method of embodiment 84, wherein the genomic locus of interest comprises the Sry locus. 86. A method for modifying a target genomic locus on the Y chromosome in a cell comprising: (a) providing a cell comprising a target genomic locus on the Y chromosome comprising a recognition site for a nuclease agent, (b) introducing into the cell (i) the se agent, wherein the nuclease agent induces a nick or -strand break at the first recognition site; and, (ii) a first targeting vector comprising a first insert polynucleotide flanked by a first and a second homology arm corresponding to a first and a second target site located in sufficient proximity to the first recognition site, wherein the length of the first gy arm and/or the second homology arm is at least 400 bp but less than 1000 bp; and, (c) identifying at least one cell comprising in its genome the first insert polynucleotide integrated at the target genomic locus. 87. The method of embodiment 86, wherein the length of the first homology arm and/or the second homology arm is from about 700 bp to about 800 bp. 88. The method of embodiment 86, wherein the modification comprises a deletion of an nous nucleic acid sequence. 89. The method of embodiment 88, n the deletion ranges from about 5 kb to about 10 kb, from about 10 kb to about 20 kb, from about 20 kb to about 40 kb, from about 40 kb to about 60 kb, from about 60 kb to about 80 kb, from about 80 kb to about 100 kb, from about 100 kb to about 150 kb, or from about 150 kb to about 200 kb, from about 200 kb to about 300 kb, from about 300 kb to about 400 kb, from about 400 kb to about 500 kb, from about 500 kb to about 1 Mb, from about 1 Mb to about 1.5 Mb, from about 1.5 Mb to about 2 Mb, from about 2 Mb to about 2.5 Mb, or from about 2.5 Mb to about 3 Mb. 90. The method of embodiment 88, wherein the deletion is at least 500 kb.

The t methods and compositions may be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will satisfy able legal requirements. Like numbers refer to like elements hout.

Many modifications and other embodiments of the methods and compositions set forth herein will come to mind to one skilled in the art to which this methods and compositions pertains having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the s and compositions are not to be limited to the specific embodiments disclosed and that modifications and other embodiments are included within the scope of the appended claims. gh specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.

The following examples are offered by way of illustration and not by way of limitation.

EXAMPLES Example 1. Targeting of the Y Chromosome Gene S[y Assisted by TALENs or CRISPR A targeted deletion comprising a lacZ replacement allele for Sry was created with a ing vector comprising, in order, an upstream homology arm of approximately 700 bp, a alactosidase coding sequence (lacZ) followed by a polyadenylation signal, a neomycin resistance cassette ﬂanked by loxP sites comprising a human ubiquitin C promoter, including the first exon, first intron, and part of the second exon, a neomycin phosphotransferase coding sequence, and a enylation signal, and a downstream homology arm of approximately 650 bp. The allele created by t targeting of the Sry gene with the targeting vector comprises a deletion of the approximately 1 kb Sry open [Link] http://www.velocigene.com/komp/detail/12778 [Link] http://www.velocigene.com/komp/detail/12778 reading frame and replacement with the lacZ-neo cassette such that the beta-galactosidase coding sequence is fused in-frame at the Sry start codon. The targeting vector was used to target the Sry gene in both the VGB6 (a.k.a. B6A6) C57BL/6 and the VGF1 (a.k.a.

F1H4) C57BL6/129 F1 hybrid ES cell lines. VGF1 (F1H4) mouse ES cells were derived from hybrid embryos produced by ng a female C57BL/6NTac mouse to a male SvEvTac mouse. Therefore, VGF1 ES cells contain a Y some from 129S6/SvEvTac mouse. The female XY mice produced from the VGF1 cell line contain a Y chromosome derived from 129S6/SvEvTac mouse.

Example 2. TALEN- or CRISPR-induced Mutations in the Y some Gene Sry ] Deletion mutations, presumably the result of non-homologous end g (NHEJ) repair of double strand DNA breaks, ranging from 3 bp to 1.2 kb and larger were created in the Sry gene by the action of a TALEN or of CRISPR guide RNAs, in combination with Cas9 DNA endonuclease (see, . ES cells comprising the TALEN- and CRISPR-induced mutations in the Sry gene also carried random transgenic insertions of the NIH KOMP project VG12778 LTVEC ( available via internet on the world wide web (www) at the URL “velocigene.com/komp/detail/12778”), which comprises a deletion of the Sry coding ce and replacement with an insertion cassette comprising lacZ fused in-frame with the Sry start codon and a neomycin resistance gene flanked by homology arms of 38 and 37 kb and based on a BAC from the bMQ library (129S7/SvEv Brd-Hprt b-m2). The LTVEC comprises in its homology arms all the known control elements for the expression of Sry. Its lacZ-encoded beta-galactosidase serves as a reporter for the tissue-specific and pmental specific expression of the Sry gene. TALEN- and CRISPR-induced mutations accompanied by LTVEC insertions were created in both the VGB6 (a.k.a. B6A6) and VGF1 (a.k.a. F1H4) ES cell lines.

We obtained a TALEN (TALEN-1) designed to target part of the HMG box DNA binding motif coding sequence (upstream recognition sequence: 5´- TCCCGTGGTGAGAGGCAC-3´ (SEQ ID NO. 72); downstream recognition sequence: 5´- TATTTTGCATGCTGGGAT-3´ (SEQ ID NO. 73) in the Sry gene. TALEN-1 was active in creating NHEJ ons at the Sry locus in multiple experiments.

Both VGB6 and VGF1 mouse ES cells were created with TALEN-induced mutations. Table 1 contains a list of all the clones and the sizes of the on mutations they carry. (ND in Table 1 indicates that a mutation was detected by a qPCR assay, but the exact molecular nature of the mutation was not determined.) All clones also carry at least one copy of the NIH KOMP project VG12778 LTVEC.

Table 1 TALEN- and CRISPR-induced mutations in the Sry gene ES cell Clone Mutation inducing agent Deletion (bp) VGB6 DE7 TALEN- 1 9 DEl 1 TALEN- 1 303* DG5 TALEN- 1 627 DH1 TALEN- 1 ND EA2 TALEN- 1 ND ED4 TALEN- 1 > 1200 EF4 TALEN- 1 16 EG7 TALEN-l >1200 VGB6 RD3 TALEN- 1 >1200 RE9 TALEN- 1 ND RF3 TALEN- 1 9 RG7 TALEN- 1 15 SF7 TALEN- 1 3 SGl 1 TALEN- 1 6 SH2 TALEN- 1 >200 SHl 1 TALEN- 1 2 VGFl TB1 TALEN- 1 1 1 TC2 TALEN-l 5 UA5 TALEN- 1 15 UB5 TALEN- 1 1201 UE12 TALEN- 1 9 WEI 1 TALEN- 1 >1200 VGB6 0G6 -2 9 QE8 CRISPR-3 5 VGFl AU-B6 CRISPR-4 5 AU-C12 CRISPR-4 8 AW-H5 -S 22 *Also contained a 50 bp insertion The results of microinjections of the Sry mutant clones are set forth in Table 2 and the breeding results of sex-reversed females are set forth in Table 3.

Table 2 F0 generation VelociMice produced by njection of Sry mutant ES cell clones into 8—cell embryos ES Cell Clone Sry mutation Female VM Male VM VGB6 ED4 >1 kb deletion 2 O EG7 >1 kb deletion 19 O GB4 None 3 GGl None 5 DEll 303 bp deletion; 50 bp insertion O DG5 627 bp deletion ll 0 VGFl TA3 None 0 5 TA4 None 0 l l TBl 11 bp deletion 2 0 TC2 5 bp deletion 8 O TH4 None 2 6 UB5 1,201 bp deletion 6 0 WEll >1.2 kb deletion 7 0 UA5 15 bp deletion 4 O UE12 9 bp deletion 8 O Table 3 Breeding results of XY female VelociMice with mutations in the Sry gene 2:11 SW Elgéetion Clone XYIlSeglale 86 Pups born VGB6 EG7 >1,200 1460403 0 1460404 0 1460405 0 1460406 1 0* 1460408 0 1460409 0 1460410 0 VGB6 DG5 627 1460428 0 1460429 0 1460430 0 1460431 0 1460432 0 1460436 0 1460437 0 1460438 0 1460410 0 VGF1 UB5 1,201 1525585 5 33 6 5 25 1525587 5 32 1525588 3 35 1525589 3 19 VGF1 WE11 >1,200 1525573 3 4 1525574 5 21 4 11 1525576 4 14 1525577 4 16 1525578 2 4 1525579 2 6 VGF1 TB1 11 1525700 5 30 1525701 4 28 VGF1 TC2 5 1525706 1 2 1525707 5 10 1525708 1 6 1525709 4 17 0 1 3 1525711 3 9 1525712 4 12 1525713 2 7 VGF1 UA5 15 1594102 2 5 1594103 2 7 WO 00805 4 1 3 1594105 2 15 VGF1 UE12 9 1594117 1 6 8 2 12 1594119 1 11 1594120 2 8 1594121 2 21 1594122 2 15 1594123 2 10 *XY Female ID# 6 had to be euthanized before birth because she had a near—term crisis and could not deliver. Her dead pups (4 male, 5 females) were recovered by dissection and none carried the Sry mutation.

] All of the VelociMice with Sry mutations derived from VGB6 ES cells were female, as ed for inactivation of Sry (Table 2). Those without Sry mutations but carrying at least one copy of the NIH KOMP VG12778 LTVEC produced only male VelociMice (Table 2, clones GB4 and GGl). When 17 Sry mutant female B6 VelociMice were test bred, only one became pregnant after about four months of breeding set-up (Table 3), and that female had to be euthanized before birth because she had a near-term crisis and could not deliver. Her dead pups (4 male, 5 females) recovered by dissection were all WT; none d the Sry mutation. It was concluded that nearly all Sry mutant mice made from VGB6 ES cells are sterile, which is in agreement with the literature on Sry mutations.

However, our data demonstrated very different result with the VGF1 clones.

First, the VGF1 ES cells were maintained, as usual, in our KO-DMEM-like low osmotic strength growth medium that is zing: some of the microinj ected XY clones grown in this medium will produce fertile XY females, i.e. an XY female phenomenon, even though they do not carry mutations. An example is clone TH4, which has no Sry mutation but carries at least one copy of the NIH KOMP VG12778 LTVEC. This clone produced 2 female and 6 male VelociMice (Table 2). Two other VGF1 clones with no Sry mutations (TA3 and TA4, Table 2) produced only male VelociMice. We wanted to determine if VGF1 XY ES cells with mutations in Sry might also be feminized by the medium. In other words, would they, unlike the VGB6 Sry mutant ES cells, produce some fertile XY Sry mutant females? (Note that VGB6 ES cells cannot be maintained in KO-DMEM-like low c strength media and retain the ability to produce mice.) The answer is yes as shown in Table Six VGF1 ES cell clones with TALEN-induced small deletions ranging from 5 bp to over 1 kb were microinjected. All produced female VelociMice, 32 of which were bred.

Remarkably, all of the Sry mutant XY female VelociMice were fertile; each produced at least one litter (Table 3). Many of the Sry mutant XY females produced multiple litters with normal litter sizes, while some of the XY females ed only one or two small litters. Out of 299 F1 mice from these breedings that have been genotyped, approximately half (146, 49%) are normal XY males or normal XX females. 174 (58%) of the F1 mice were phenotypic females, while 125 (42%) were ypic males. 26 of the females (15% of females, 8.7% of the total F1 generation) were XY females that inherited a mutant Sry allele.

Because of meiotic non-disjunction events associated with XY oocytes, a number of aberrant genoytpes — XXY, XYY, XO, XXYY — some of which included mutant Sry alleles were observed in the F1 progeny of Sry mutant XY female VelociMice.

A method for the efficient on of fertile XY female VelociMice from XY ES cells has been discovered. If inactivating mutations in the Sry gene in ES cells are created that have been maintained in the feminizing growth medium, a high tion of fertile XY female mice are obtained that when bred to males produce mostly male and female mice with normal X and Y chromosomes. e 3. Embryo recovery in KO-DMEM or DMEM after TALEN-induced Mutations in the Y Chromosome Gene Sry Correct targeting of mouse Sry by LTVEC was confirmed or negated by genotyping of F1 offspring derived from F0 females, which were XY and carried Sry mutation. Co-segregation in F1 mice of the LacZ/Neo cassette with the Sry mutation (as assessed by Sry LOA assays) strongly suggests t targeting. Failure of LacZ/Neo to co- segregate with the on indicates that the original clone contained an Sry deletion mutation (induced by TALEN) coupled with a LacZ/Neo transgenic ion elsewhere in the genome.

Offspring from XY females with Sry mutations exhibited a variety of abnormal karyotypes at a high frequency (including XXY, XYY, and X0). Sex some count was ed by using unrelated loss of allele (LOA) assays for genes on X and Y chromosomes.

The copy number of Sry was then ined using LOA assays. The presence of mutant Sry allele was inferred in mice in which the Y chromosome copy number exceeded the Sry copy number (for instance, 1 copy of Y and 0 copies of Sry, or 2 copies of Y and 1 copy of Sry).

Lastly the presence of LacZ and Neo were ined using TaqMan assays.

In the original set of clones, which were created by Sry LTVEC er with TALEN nuclease and grown in KO-DMEM, it was evident that LacZ/Neo cassette was not co-segregating with the Sry mutation. A sample litter from these clones is shown in Table 4. 2015/038001 Table 4: Screening of clones generated by Sry LTVEC together with TALEN nuclease Mouse SeX X Chr Y Chr Sry LacZ Neo Genotype Comments Copy # Copy # Copy 1656721 M 1 1 1 X+Y+ 1656722 M 1 1 1 X+Y+ LacZ/Neo present by Sry mutation absent 1656723 M 1 1 1 0 0 X+Y+ 1656724 M 1 2 1 0 0 X+Y+YA Sry mutation present but LacZ/Neo absent F 2 0 0 X+X+ LacZ/Neo present but Sry mutation absent 6 F 2 1 0 X+X+ Sry mutation YA t but LacZ/Neo absent 1656727 F 2 1 0 X+X+ 1656728 F 1 0 0 X+ LacZ/Neo present but Sry mutation absent 1656729 F 1 0 0 X+ In the subsequent set of , which were created by Sry LTVEC together with TALEN nuclease and grown in DMEM, the LacZ/Neo cassette was completely co- ating with the Sry mutation, indicating correct targeting. A typical litter from these clones is shown in Table 5.

Table 5: Screening results for clones created by Sry LTVEC together with TALEN nuclease Mouse SeX X Chr Y Chr Sry LacZ Neo Genotype Copy # Copy # Copy 1848360 M 1 1 1 0 0 X+Y+ 1848361 M 1 1 1 0 0 X+Y+ 1848362 M 1 1 1 0 0 X+Y+ 1848363 1 1 0 0 1848364 1 1 1848365 1848366 1848367 2015/038001 Example 4: TALEN and CRISPR-Assisted ing of Sry by SmallTVECs or LTVECs As depicted in a targeted deletion sing a lacZ replacement allele for Sry was created with either a LTVEC or a small targeting vector (smallTVEC) together with either TALEN nuclease or CRISPR guide RNAs, in combination with Cas9 DNA endonuclease. The VEC comprised, in order, an upstream homology arm of approximately 700-800 bp, a beta-galactosidase coding sequence (lacZ) followed by a polyadenylation signal, a neomycin resistance cassette ﬂanked by loxP sites comprising a human ubiquitin C promoter, including the first exon, first intron, and part of the second exon, a neomycin phosphotransferase coding sequence, and a polyadenylation signal, and a downstream homology arm of approximately 700-800 bp. The allele created by correct targeting of the Sry gene with the targeting vector comprises a deletion of the approximately 1 kb Sry open reading frame and replacement with the lacZ-neo cassette such that the beta- galactosidase coding sequence is fused in-frame at the Sry start codon. The ing vector was used to target the Sry gene in the VGFl (a.k.a. FlH4) /129 F1 hybrid ES cell line and in the VGB6 ES cell line (a.k.a. B6A6).

As illustrated in Table 6, clones produced using four different gRNAs and one TALEN pair were produced and screened for cleavage and loss of allele by TaqMan assays.

Table 6: Screening results for cleavage and loss of allele Small TVEC Targeting Location Clones Total targ. Eff.

Screened (%) HMG box 192 2.1 HMG box 192 2.6 3’ end 192 1.6 3’ end gRNA 5 192 2.6 HMG box TALEN pair 1 384 0.3 The LTVEC transgenic clones produced embryos with the same lacZ pattern. rates LacZ expression in the embryos.

Table 7 reports the fertility results of XY Females derived from ES cells grown in conventional DMEM-based medium that had TALEN-assisted LTVEC targeted deletion- replacement mutations of Sry. Unexpectedly compared with the results for a similar ment with ES cells grown in KO-DEMEM-based medium (Table 3), LTVEC targeting in DMEM-based medium produced clones with tly targeted Sry deletions and lacZ—neo ions. Forty out of 41 XYS'WQCZ) females derived from four targeted clones produced live born pups upon mating — a 98% fertility rate. Thus, we have d two new ways to produce highly fertile XY females from mutant ES cells: (1) TALEN-induced inactivating mutations in Sry in ES cells grown in a KO-DMEM-based medium; and (2) TALEN-assisted LTVEC targeted precise on-replacement mutations in ES cells grown in DMEM-based medium.

Table 7: Production of Sry TALEN Mutant XY Females Clone ES Allele XY female XY Fertile Fertility cell description VelocMice females XY rates line bred females (%) X-C4 VGFl lacZ—neo 2 2 100 targeted X-El 0 VGFl lacZ—neo 1 1 1 100 XOF3 VGFl lacZ—neo 2 5 3 3 100 m targeted 2 X-G3 VGFl lacZ—neo Q 9 3 2 67 targeted VGFl Total 53 41 40 98 Example 5: Large on on the Y Chromosome Mediated by ZFNs As illustrated in large deletions, 500 kb or greater, were made on the Y chromosome using ZFNs targeting the Kdm5d and the Usp9y genes. Table 8 provides examples of zinc finger sequences on the Y chromosome.

Table 8: Zinc Finger Sequence on the Y Chromosome Target SEQ ID Y CHR Plate ch Fmger Sequence_ _ ZFN# Name N0: ZFN1 42 NMOll419—r43102al ttAGGTAGGTAGACAGGGATgttttctg KDMSD NMOll419—43108al atCCAGTCtCTGAAGGAAGCTctgacta 19—rl9880al caAAAGCTTCAGGGGGActcttacactc NMOll419—19887al ttTGAGCAgGCTACACAGGAGtatactt ZFNS 46 —rl7347al aaGCGGTGgCAATAGGCAaaagatgtgg 011419—17353al ctGAAGTCCCCAAGGGAGTAtggagatg Oll4lg—rl7350al agAAAGCGGTGGCAaTAGGCAaaagatg 011419—17356al aaGTCCCCAAGGGAGTAtggagatgccc 012008—r8130al acTCCAACGACTATGACcactccgttca 012008—8136al acAGATCAGATGAAGATgactggtcaaa 012008—r7l72al ctTTCAAGGAAAAAAAGaacaaaaccca DDX3Y 012008—7178al ggTCTGTGATAAGGACAGTTcaggatgg —r20472al taAATCTGACTGAGAATGGGtagtagaa 012008—20479al caGATGGTCCAGGAGAGGCTttgaaggc 012008—r7267al atTGGGCTTCCCTCTGGAatcacgagat OlZOO8—7274al ttTCAGTGATCGTGGAAGTGgatccagg l48943—r9256lal ctGGTTTGGAAATCGTActgtaaaagac l48943—92567al gcAAAGAGGTTGAGGATttggacatatt l48943—r11830al gaGGAGTTGTTGGAGAAGTthattgga [JSPQY l48943—ll836al atATGAACAAGGCCAAthgatgctcca l48943—r108581al aCTCAGAAGAAGGATTAGGAatgctttg 148943—108588al AGaAATGTATCAGTTcatcttg l48943—rl6244al tcCATAAGGATTTTGGAaaaagacacag ZFN8 65 l48943—l6251al agGCTGTGAGTGGATGGAAGtttgaaat In one experiment, 3.3 million ES cells from VGB6 clones D-G5 and E-G7 (Table 3) were electroporated with the ZFN mRNA pairs Kdm5d-ZFN5(NM01 1419- rl7347al)/ZFN6(NM01l4l9-l7353al) and Usp9y-ZFN3(NM148943- al)/ZFN4(NM148943-l1836al) (10 ug each) and with an LTVEC targeting the Ch25h gene (0.67 ug), to provide selection for cin resistance. Puromycin resistant colonies were picked and screened for the deletion. The results are shown in Table 9.

Table 9: Screening Results for large Y chromosome deletion in 12778D-G5 and 12778E-G7 Parental Clone # of Puromycin- # of Colonies # Confirmed d resistant Colonies Screened Clones 12778E-G7 638 384 8 2015/038001 Table 10 shows the exact sizes of the r than 500 kb deletions that were precisely determined for one deletion clone (4306A-D5) derived from the E-G7 parental clone (Table 3) and two deletion clones (4306E-C4 and 4306F-A12) derived from the D-G5 parental clone (Table 3).

Table 10: ZEN-mediated deletions of Kdm5d and Usp9y Deletion Coordinates Clone Size (bp) on Y some 4306A-D5 -785404 534835 4306E-C4 520363-785402 535039 4306F—A12 250373-785404 535031 on of the Kdm5d, Eif2s3y, Uty, Ddx3y, and Usp9y genes ( was confirmed in the deletion loss-of-allele assays and DNA sequencing as shown in Clone 4306A-D5 produced nine XY female fully ES cell-derived VelociMice upon microinjection into 8-cell stage embryos and transfer to surrogate mothers. None of the XY females from clone 4306A-D5 were fertile.

Example 6: Large on on the Y Chromosome Mediated by CRISPR/Cas A large deletion of the on the Y chromosome targeting the region n the Kdm5d and the Usp9y genes was made utilizing CRISPR guide RNAs in combination with Cas9 DNA endonuclease. gRNAs were designed to target the Kdm5d gene and the Usp9y gene. The following gRNAs were designed to target Kdm5d: Kdm5dgA (Guide #1) UUUGCCGAAUAUGCUCUCGU (SEQ ID NO:66); Kdm5ng (Guide #2) UUGCCGAAUAUGCUCUCGUG (SEQ ID NO:67); and Kdm5dgC (Guide #5) CGGGCAUCUCCAUACUCCCU (SEQ ID NO:68). The following gRNAs were designed to target Usp9y: Usp9ygA (Guide #1) UAGCUCGUUGUGUAGCACCU (SEQ ID ; Usp9ygB (Guide #1) UAUAGUUUCUUCGGGGUAAC (SEQ ID NO:70); and Usp9ng (Guide #2) CCUUCUAUAGGCCC (SEQ ID NO:7l).

VGFl mouse ES cells were electroporated with 5 ug of a plasmid that expressed Cas9 and 10 ug each of plasmids that expressed the Kdm5d gRNA B and Usp9y gRNA C and with an LTVEC targeting the Ch25h gene (0.67 ug), to provide selection for puromycin resistance. .

As illustrated in Kdm5ng (gRNA B) and Usp9ng (gRNA C) were used to target the deletion of the Kdm5d and Usp9y genes. The resulting clones were ed for deletion by loss-of-allele assays for sequences at the Kdm5d and Usp9y genes and the genes in between (Eif2s3y, Uly, and Ddx3y) and for genes outside the targeted deletion (ny2 and Sry). As shown in Table 11, four clones comprising the large deletion were obtained. Clone R-AS produced seven XY male and 3 XY female fully ES cell-derived VelociMice upon microinjection into 8-cell stage s and transfer to surrogate mothers.

Table 11: TaqMan assay confirming large on mediated by CRISPR guide RNAs and Cas9 Loss-of—allele Copy Number Determination Clone 19178TD 16697TD F12 Note Zjﬁ/Z Sry (1317253y) Large Q_F1 0 1 deletion R-A8 o 1 Large deletion Large R-C2 0 1 deletion, partial loss Y clone add as R4511 1 1 WT l All publications and patent applications ned in the specification are indicative of the level of those skilled in the art to which this invention pertains. All ations and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference. If the information associated with a citation, such as a deposit number changes with time, the version of the information in effect at the effective filing date of the application is intended, the effective filing date meaning the actual filing date or date of a priority application first providing the citation. Unless otherwise apparent from the context of any embodiment, aspect, step or feature of the invention can be used in ation with any other. nce to a range includes any integers within the range, any subrange within the range. Reference to multiple ranges includes composites of such ranges.

Claims

THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:

1. A method for making a mouse XY embryonic stem (ES) cell line capable of producing a fertile XY female mouse in an F0 generation, sing: (a) modifying a mouse XY ES cell to comprise a c modification comprising a deletion that inactivates an endogenous Sry gene, n the mouse XY ES cell comprises a Y chromosome from a 129S6 strain; and (b) culturing the modified mouse XY ES cell under conditions to produce the mouse XY ES cell line e of producing the fertile XY female non-human mammal in the F0 generation.

2. The method of claim 1, wherein the genetic modification is generated by introducing into the mouse XY ES cell a nuclease agent that induces a nick or a double-strand break at a recognition site on the Y chromosome or a polynucleotide encoding the nuclease agent.

3. The method of claim 2, wherein the nuclease agent is a zinc finger se (ZFN), a Transcription Activator-Like Effector Nuclease (TALEN), a clease, or a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated (Cas) protein and a guide RNA (gRNA).

4. The method of claim 3, wherein the nuclease agent is the Cas protein and the gRNA, wherein the Cas protein is a Cas9 protein, and wherein the gRNA comprises: (a) a CRISPR RNA (crRNA) that targets the recognition site, wherein the recognition site is immediately flanked by a Protospacer Adjacent Motif (PAM) sequence; and (b) a activating CRISPR RNA (tracrRNA), optionally wherein the gRNA targets a sequence comprising SEQ ID NO: 10, SEQ ID NO: 11, or SEQ ID NO: 12.

5. The method of claim 3, n the se agent is the TALEN, optionally wherein the TALEN targets a sequence comprising SEQ ID NO: 72 and a sequence sing SEQ ID NO: 73.

6. The method of any one of claims 1-5, wherein the genetic modification is generated by introducing into the mouse XY ES cell a targeting vector comprising an insert polynucleotide flanked by first and second gy arms corresponding to first and second target sites at a target genomic locus on the Y chromosome, wherein the mouse XY ES cell is modified to comprise the insert polynucleotide at the target genomic locus.

7. The method of claim 6, wherein the first homology arm is from about 400- 1000 base pairs, and the second homology arm is from about 00 base pairs.

8. The method of claim 6, wherein the sum total of the first homology arm and the second gy arm is at least 10 kb.

9. The method of any one of claims 6-8, wherein the genetic modification is generated by introducing into the mouse XY ES cell: (i) a nuclease agent that induces the nick or a double-strand break at the recognition site on the Y chromosome or a polynucleotide encoding the nuclease agent; and (ii) the targeting vector comprising the insert polynucleotide flanked by first and second homology arms corresponding to first and second target sites at the target genomic locus on the Y chromosome, wherein the mouse XY ES cell is modified to comprise the insert polynucleotide at the target genomic locus.

10. The method of any one of claims 1-9, wherein the mouse XY ES cell is not cultured in a feminizing medium.

11. The method of any one of claims 1-9, wherein the culturing step comprises culturing the modified mouse XY ES cell in a medium comprising: (1) a base medium comprising about 3 mg/mL sodium chloride and about 2.2 mg/mL sodium bicarbonate and having an osmolality of about 218 mOsm/kg; and (2) supplements that maintain the modified mouse XY ES cell in culture.

12. The method of any one of claims 1-11, wherein upon introduction of the modified mouse XY ES cell into a mouse host embryo and following ion of the mouse host embryo to e F0 mice, at least 60% of the F0 mice are XY s which upon attaining sexual maturity are fertile.

13. A method for making a fertile XY female mouse in an F0 tion, comprising: (a) ucing a mouse XY embryonic stem (ES) cell into a mouse host embryo, wherein the mouse XY ES cell comprises a Y chromosome from a 129S6 strain and a genetic modification comprising a deletion that vates an endogenous mouse Sry gene, and ally wherein the mouse host embryo is a rula stage embryo; (b) gestating the mouse host embryo; and (c) obtaining F0 mice following gestation of the mouse host embryo, wherein at least 60% of the F0 mice are XY females which upon attaining sexual maturity are fertile.

14. The method of claim 13, wherein the F0 XY female mouse is fertile when crossed to a wild-type mouse, optionally wherein the wild-type mouse is a C57BL/6 mouse.

15. The method of any one of claims 1-14, wherein the mouse XY ES cell is isolated from a mouse that is a cross between a 129S6 strain and a C57BL/6 strain.

16. The method of claim 15, wherein the mouse XY ES cell is isolated from a hybrid embryo produced by ng a female C57BL/6NTac mouse to a male 129S6/SvEvTac mouse.

17. The method of claim 16, wherein the mouse XY ES cell is a VGF1 mouse ES cell.

18. The method of any one of claims 1-17, wherein the genetic modification further comprises an insertion of one or more nucleotides, a substitution of one or more nucleotides, or a combination thereof, optionally wherein: (I) the genetic modification further comprises a knockout; a knockin; a replacement of an endogenous nucleic acid sequence with a homologous, orthologous, or heterologous sequence; or a combination thereof; (II) the genetic modification further comprises an ion of a nucleic acid encoding a able marker and/or a nucleic acid ng a reporter gene operably linked to a promoter active in the mouse XY ES cell; or (III) the genetic modification further comprises an insertion of a nucleic acid encoding a reporter gene ly linked to an endogenous Sry promoter.

19. The method of any one of claims 1-18, further comprising modifying the mouse XY ES cell to comprise at least one additional ed genetic modification of a polynucleotide of interest.

20. The method of any one of claims 12-19, wherein upon introduction of the modified mouse XY ES cell into the mouse host embryo and following gestation of the mouse host embryo, at least 80% of the F0 mice are XY females which upon attaining sexual maturity are fertile, optionally wherein at least 90% of the F0 mice are XY females which upon attaining sexual maturity are fertile, and optionally wherein at least 95% of the F0 mice are XY females which upon attaining sexual maturity are fertile.

21. A cell produced by the method of any one of claims 1-12.

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