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{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
'''Spo11''' is a [[protein]] that in humans is encoded by the ''SPO11'' [[gene]]. Spo11, in a complex with mTopVIB, creates double strand breaks to initiate meiotic [[genetic recombination|recombination]].<ref>{{cite journal | vauthors = Vrielynck N, Chambon A, Vezon D, Pereira L, Chelysheva L, De Muyt A, Mézard C, Mayer C, Grelon M | display-authors = 6 | title = A DNA topoisomerase VI-like complex initiates meiotic recombination | journal = Science | volume = 351 | issue = 6276 | pages = 939–43 | date = February 2016 | pmid = 26917763 | doi = 10.1126/science.aad5196 | bibcode = 2016Sci...351..939V | s2cid = 206643600 | url = https://www.science.org/doi/10.1126/science.aad5196 }}</ref><ref>{{cite journal | vauthors = Robert T, Nore A, Brun C, Maffre C, Crimi B, Bourbon HM, de Massy B | title = The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation | journal = Science | volume = 351 | issue = 6276 | pages = 943–9 | date = February 2016 | pmid = 26917764 | doi = 10.1126/science.aad5309 | bibcode = 2016Sci...351..943R | s2cid = 9445593 | url = https://www.science.org/doi/10.1126/science.aad5309 }}</ref> Its active site contains a tyrosine which ligates and dissociates with DNA to promote break formation. One Spo11 protein is involved per strand of DNA, thus two Spo11 proteins are involved in each double stranded break event.
Genetic exchange between two DNA molecules by [[homologous recombination]] begins with a break in both strands of DNA—called a double-strand break—and recombination is started by an [[endonuclease]] enzyme that cuts the DNA molecule that "receives" the exchanged DNA. In [[meiosis]] the enzyme is SPO11, which is related to DNA [[topoisomerase]]s. Topoisomerases change DNA by transiently breaking one or both strands, passing the unbroken DNA strand or strands through the break and repairing the break; the broken ends of the DNA are covalently linked to topoisomerase. SPO11 is similarly attached to the DNA when it forms double-strand breaks during meiosis.<ref name="isbn0-7637-7992-X">{{cite book |title=Lewin's Genes X |edition=10th |publisher=Jones and Bartlett Publishers, Inc. |location= |year=2011 |origyear= |pages=353–354 |isbn=0-7637-7992-X |oclc= |doi= |url= |accessdate=}}</ref>▼
▲Genetic exchange between two DNA molecules by [[homologous recombination]]
==Meiotic recombination independent of SPO11==▼
SPO11 is considered to play a predominant role in initiating [[Meiosis|meiotic]] recombination. However, recombination may also occur by alternative SPO11-independent mechanisms that can be studied experimentally using ''spo11'' mutants.
In the budding yeast ''
In the worm ''Caenorhabditis elegans'', a homolog of ''spo11'' is ordinarily employed in the initiation of meiotic recombination. However, radiation induced-breaks can also initiate recombination in mutants deleted for this ''spo11'' homolog.<ref name="pmid9708740">{{cite journal | vauthors = Dernburg AF, McDonald K, Moulder G, Barstead R, Dresser M, Villeneuve AM | title = Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis | journal = Cell | volume = 94 | issue = 3 | pages = 387–98 |
[[Deamination]] of cytosine resulting in the dU:dG mismatch is one of the most common single-base-altering lesions in non-replicating DNA. ''Spo11'' mutants of the fission yeast ''Schizosaccharomyces pombe'' and ''C. elegans'' undergo meiotic crossover recombination and proper chromosome segregation when dU:dG lesions are produced in their DNA.<ref name=Pauklin>{{cite journal | vauthors = Pauklin S, Burkert JS, Martin J, Osman F, Weller S, Boulton SJ, Whitby MC, Petersen-Mahrt SK | display-authors = 6 | title = Alternative induction of meiotic recombination from single-base lesions of DNA deaminases | journal = Genetics | volume = 182 | issue = 1 | pages = 41–54 |
In ''S. pombe'', a mutant defective in the ''spo11'' homolog ''Rec12'' is deficient in meiotic recombination. However recombination can be restored to near normal levels by a deletion in ''rad2'', a gene that encodes an endonuclease involved in [[Okazaki fragments|Okazaki fragment]] processing (Farah et al., 2005). Both crossover and non-crossover recombination were increased but double-strand breaks were undetectable. On the basis of the biochemical properties of the rad2 deletion, it was proposed that meiotic recombination can be initiated by DNA lesions other than double-strand breaks, such as nicks and gaps which accumulate during premeiotic DNA replication when Okasaki fragment processing is deficient.<ref name="pmid16118186">{{cite journal | vauthors = Farah JA, Cromie G, Davis L, Steiner WW, Smith GR | title = Activation of an alternative, rec12 (spo11)-independent pathway of fission yeast meiotic recombination in the absence of a DNA flap endonuclease | journal = Genetics | volume = 171 | issue = 4 | pages = 1499–511 |
The above findings indicate that DNA damages arising from a variety of sources can be repaired by meiotic recombination and that such a process can occur independently of SPO11.
== Absence
The most recent common ancestor of the social [[amoeba]] genera ''[[Dictyostelium]]'', ''[[Polysphondylium]]'' and ''[[Acytostelium]]'', appears to have lacked the ''Spo11'' gene.<ref name=Bloomfield>{{cite journal | vauthors = Bloomfield G | title = Atypical ploidy cycles, Spo11, and the evolution of meiosis | journal =
== References ==
{{Reflist|colwidth=30em}}
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