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Chapter 14 AP Biology Outline

Gregor Mendel conducted experiments breeding pea plants that revealed the basic principles of heredity. By tracking inherited traits over multiple generations, Mendel discovered that traits are inherited in discrete units, which he called factors (now called genes). Mendel showed that these factors segregate, or separate, during gamete formation and transmission from parents to offspring in a predictable statistical pattern. His work formed the basis of classical genetics and resolved the debate between blending versus particulate theories of inheritance.

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0% found this document useful (0 votes)
573 views15 pages

Chapter 14 AP Biology Outline

Gregor Mendel conducted experiments breeding pea plants that revealed the basic principles of heredity. By tracking inherited traits over multiple generations, Mendel discovered that traits are inherited in discrete units, which he called factors (now called genes). Mendel showed that these factors segregate, or separate, during gamete formation and transmission from parents to offspring in a predictable statistical pattern. His work formed the basis of classical genetics and resolved the debate between blending versus particulate theories of inheritance.

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Chapter14

MendelandtheGeneIdea
LectureOutline
Overview
Everydayweobserveheritablevariations(suchasbrown,green,orblueeyes)among
individualsinapopulation.

Thesetraitsaretransmittedfromparentstooffspring.

Onepossibleexplanationforheredityisablendinghypothesis.
Thishypothesisproposesthatgeneticmaterialcontributedbyeachparentmixesina
manneranalogoustothewayblueandyellowpaintsblendtomakegreen.
Withblendinginheritance,afreelymatingpopulationwilleventuallygiverisetoa
uniformpopulationofindividuals.
Everydayobservationsandtheresultsofbreedingexperimentstellusthatheritabletraits
donotblendtobecomeuniform.

Analternativemodel,particulateinheritance,proposesthatparentspassondiscrete
heritableunits,genes,thatretaintheirseparateidentitiesinoffspring.
Genescanbesortedandpassedon,generationaftergeneration,inundilutedform.
Moderngeneticsbeganinanabbeygarden,whereamonknamedGregorMendel
documentedaparticulatemechanismofinheritance.
A.GregorMendelsDiscoveries
1.Mendelbroughtanexperimentalandquantitativeapproachtogenetics.
Mendeldiscoveredthebasicprinciplesofhereditybybreedinggardenpeasincarefully
plannedexperiments.

MendelgrewuponasmallfarminwhatistodaytheCzechRepublic.

In1843,MendelenteredanAugustinianmonastery.

HestudiedattheUniversityofViennafrom1851to1853,wherehewasinfluencedbya
physicistwhoencouragedexperimentationandtheapplicationofmathematicstoscienceand
byabotanistwhostimulatedMendelsinterestinthecausesofvariationinplants.

TheseinfluencescametogetherinMendelsexperiments.

Afteruniversity,MendeltaughtattheBrunnModernSchoolandlivedinthelocal
monastery.
Themonksatthismonasteryhadalongtraditionofinterestinthebreedingofplants,
includingpeas.

Around1857,Mendelbeganbreedinggardenpeastostudyinheritance.

Peaplantshaveseveraladvantagesforgeneticstudy.
IG Lecture Outline 14-1

Peaplantsareavailableinmanyvarietieswithdistinctheritablefeatures,orcharacters,
withdifferentvarianttraits.
Mendelcouldstrictlycontrolwhichplantsmatedwithwhich.
Eachpeaplanthasmale(stamens)andfemale(carpal)sexualorgans.
Innature,peaplantstypicallyselffertilize,fertilizingovawiththespermnucleifrom
theirownpollen.
However,Mendelcouldalsousepollenfromanotherplantforcrosspollination.

Mendeltrackedonlythosecharactersthatvariedinaneitherormanner,ratherthana
moreorlessmanner.
Forexample,heworkedwithflowersthatwereeitherpurpleorwhite.
Heavoidedtraits,suchasseedweight,thatvariedonacontinuum.

Mendelstartedhisexperimentswithvarietiesthatweretruebreeding.
Whentruebreedingplantsselfpollinate,alltheiroffspringhavethesametraits.

Inatypicalbreedingexperiment,Mendelwouldcrosspollinate(hybridize)two
contrasting,truebreedingpeavarieties.
ThetruebreedingparentsarethePgeneration,andtheirhybridoffspringaretheF1
generation.

MendelwouldthenallowtheF1hybridstoselfpollinatetoproduceanF2generation.

ItwasmainlyMendelsquantitativeanalysisofF 2plantsthatrevealedtwofundamental
principlesofheredity:thelawofsegregationandthelawofindependentassortment.
2.Bythelawofsegregation,thetwoallelesforacharacterareseparatedduringtheformation
ofgametes.
Iftheblendingmodelwascorrect,theF1hybridsfromacrossbetweenpurpleflowered
andwhitefloweredpeaplantswouldhavepalepurpleflowers.
Instead,F1hybridsallhavepurpleflowers,justaspurpleastheirpurpleflowered
parents.
WhenMendelallowedtheF1plantstoselffertilize,theF2generationincludedboth
purplefloweredandwhitefloweredplants.
Thewhitetrait,absentintheF1,reappearedintheF2.

Mendelusedverylargesamplesizesandkeptaccuraterecordsofhisresults.
Mendelrecorded705purplefloweredF2plantsand224whitefloweredF2plants.
ThiscrossproducedatraitsratioofthreepurpletoonewhiteintheF 2offspring.

MendelreasonedthattheheritablefactorforwhiteflowerswaspresentintheF 1plants,
butdidnotaffectflowercolor.
Purpleflowercolorisadominanttrait,andwhiteflowercolorisarecessivetrait.
ThereappearanceofwhitefloweredplantsintheF2generationindicatedthatthe
heritablefactorforthewhitetraitwasnotdilutedorblendedbycoexistingwiththepurple
flowerfactorinF1hybrids.
Mendelfoundsimilar3to1ratiosoftwotraitsamongF 2offspringwhenheconducted
crossesforsixothercharacters,eachrepresentedbytwodifferenttraits.
Forexample,whenMendelcrossedtwotruebreedingvarieties,oneproducinground
seedsandtheotherproducingwrinkledseeds,alltheF1offspringhadroundseeds.
IntheF2plants,75%oftheseedswereroundand25%werewrinkled.
IG Lecture Outline 14-2

Mendeldevelopedahypothesistoexplaintheseresultsthatconsistedoffourrelated
ideas.Wewillexplaineachideawiththemodernunderstandingofgenesandchromosomes.
1.
Alternativeversionsofgenesaccountforvariationsininheritedcharacters.
Thegeneforflowercolorinpeaplantsexistsintwoversions,oneforpurpleflowersand
oneforwhiteflowers.
Thesealternateversionsarecalledalleles.
Eachgeneresidesataspecificlocusonaspecificchromosome.
TheDNAatthatlocuscanvaryinitssequenceofnucleotides.
ThepurpleflowerandwhiteflowerallelesaretwoDNAvariationsattheflowercolor
locus.
2.
Foreachcharacter,anorganisminheritstwoalleles,onefromeachparent.
Adiploidorganisminheritsonesetofchromosomesfromeachparent.
Eachdiploidorganismhasapairofhomologouschromosomesand,therefore,two
copiesofeachgene.
Thesehomologouslocimaybeidentical,asinthetruebreedingplantsoftheP
generation.
Alternatively,thetwoallelesmaydiffer.
3.
Ifthetwoallelesatalocusdiffer,thenone,thedominantallele,determinesthe
organismsappearance.Theother,therecessiveallele,hasnonoticeableeffectonthe
organismsappearance.
Intheflowercolorexample,theF 1plantsinheritedapurpleflowerallelefromoneparent
andawhiteflowerallelefromtheother.
Theyhadpurpleflowersbecausethealleleforthattraitisdominant.
4.
4.Mendelslawofsegregationstatesthatthetwoallelesforaheritable
characterseparateandsegregateduringgameteproductionandendupindifferent
gametes.
Thissegregationofallelescorrespondstothedistributionofhomologouschromosomes
todifferentgametesinmeiosis.
Ifanorganismhastwoidenticalallelesforaparticularcharacter,thenthatalleleis
presentasasinglecopyinallgametes.
Ifdifferentallelesarepresent,then50%ofthegameteswillreceiveonealleleand50%
willreceivetheother.
Mendelslawofsegregationaccountsforthe3:1ratiothatheobservedintheF 2
generation.
TheF1hybridsproducetwoclassesofgametes,halfwiththepurplefloweralleleandhalf
withthewhiteflowerallele.

Duringselfpollination,thegametesofthesetwoclassesuniterandomly.

Thisproducesfourequallylikelycombinationsofspermandovum.

APunnettsquarepredictstheresultsofageneticcrossbetweenindividualsofknown
genotype.

LetusdescribeaPunnettsquareanalysisoftheflowercolorexample.

Wewilluseacapitallettertosymbolizethedominantalleleandalowercaseletterto
symbolizetherecessiveallele.
Pisthepurpleflowerallele,andpisthewhiteflowerallele.

WhatwillbethephysicalappearanceoftheF2offspring?
IG Lecture Outline 14-3

OneinfourF2offspringwillinherittwowhiteflowerallelesandproducewhiteflowers.
HalfoftheF2offspringwillinheritonewhitefloweralleleandonepurpleflowerallele
andproducepurpleflowers.
OneinfourF2offspringwillinherittwopurpleflowerallelesandproducepurple
flowers.

Mendelsmodelaccountsforthe3:1ratiointheF2generation.

Anorganismwithtwoidenticalallelesforacharacterishomozygousforthatcharacter.

Organismswithtwodifferentallelesforacharacterisheterozygousforthatcharacter.

Anorganismstraitsarecalleditsphenotype.

Itsgeneticmakeupiscalleditsgenotype.
Twoorganismscanhavethesamephenotypebuthavedifferentgenotypesifoneis
homozygousdominantandtheotherisheterozygous.

Forflowercolorinpeas,theonlyindividualswithwhiteflowersarethosethatare
homozygousrecessive(pp)fortheflowercolorgene.
However,PPandPpplantshavethesamephenotype(purpleflowers)butdifferent
genotypes(homozygousdominantandheterozygous).

Howcanwetellthegenotypeofanindividualwiththedominantphenotype?
Theorganismmusthaveonedominantallele,butcouldbehomozygousdominantor
heterozygous.

Theansweristocarryoutatestcross.
Themysteryindividualisbredwithahomozygousrecessiveindividual.
Ifanyoftheoffspringdisplaytherecessivephenotype,themysteryparentmustbe
heterozygous.

3.Bythelawofindependentassortment,eachpairofallelessegregatesindependentlyinto
gametes.

Mendelsfirstexperimentsfollowedonlyasinglecharacter,suchasflowercolor.
AllF1progenyproducedinthesecrossesweremonohybrids,heterozygousforone
character.
Acrossbetweentwoheterozygotesisamonohybridcross.

Mendelidentifiedthesecondlawofinheritancebyfollowingtwocharactersatthesame
time.

Inonesuchdihybridcross,Mendelstudiedtheinheritanceofseedcolorandseedshape.
Thealleleforyellowseeds(Y)isdominanttothealleleforgreenseeds(y).
Thealleleforroundseeds(R)isdominanttothealleleforwrinkledseeds(r).

Mendelcrossedtruebreedingplantsthathadyellow,roundseeds(YYRR)withtrue
breedingplantsthathasgreen,wrinkledseeds(yyrr).
Onepossibilityisthatthetwocharactersaretransmittedfromparentstooffspringasa
package.
TheYandRallelesandyandrallelesstaytogether.

Ifthiswerethecase,theF1offspringwouldproduceyellow,roundseeds.

TheF2offspringwouldproducetwophenotypes(yellow+round;green+wrinkled)ina
3:1ratio,justlikeamonohybridcross.
IG Lecture Outline 14-4

ThiswasnotconsistentwithMendelsresults.

Analternativehypothesisisthatthetwopairsofallelessegregateindependentlyofeach
other.
Thepresenceofaspecificalleleforonetraitinagametehasnoimpactonthepresence
ofaspecificalleleforthesecondtrait.

Inourexample,theF1offspringwouldstillproduceyellow,roundseeds.

However,whentheF1sproducedgametes,geneswouldbepackagedintogameteswith
allpossiblealleliccombinations.
Fourclassesofgametes(YR,Yr,yR,andyr)wouldbeproducedinequalamounts.
Whenspermwithfourclassesofallelesandovawithfourclassesofallelescombined,
therewouldbe16equallyprobablewaysinwhichtheallelescancombineintheF 2
generation.

Thesecombinationsproducefourdistinctphenotypesina9:3:3:1ratio.

ThiswasconsistentwithMendelsresults.

Mendelrepeatedthedihybridcrossexperimentforotherpairsofcharactersandalways
observeda9:3:3:1phenotypicratiointheF2generation.

Eachcharacterappearedtobeinheritedindependently.

Ifyoufollowjustonecharacterinthesecrosses,youwillobservea3:1F 2ratio,justasif
thiswereamonohybridcross.
Theindependentassortmentofeachpairofallelesduringgameteformationisnowcalled
Mendelslawofindependentassortment.
Mendelslawofindependentassortmentstatesthateachpairofallelessegregates
independentlyduringgameteformation.
Strictlyspeaking,thislawappliesonlytogeneslocatedondifferent,nonhomologous
chromosomes.
Geneslocatedneareachotheronthesamechromosometendtobeinheritedtogetherand
havemorecomplexinheritancepatternsthanthosepredictedforthelawofindependent
assortment.
4.ThelawsofprobabilitygovernMendelianinheritance.
Mendelslawsofsegregationandindependentassortmentreflectthesamelawsof
probabilitythatapplytotossingcoinsorrollingdice.
Theprobabilityscalerangesfrom0(aneventwithnochanceofoccurring)to1(anevent
thatiscertaintooccur).
Theprobabilityoftossingheadswithanormalcoinis1/2.
Theprobabilityofrollinga3withasixsideddieis1/6,andtheprobabilityofrollingany
othernumberis11/6=5/6.
Whentossingacoin,theoutcomeofonetosshasnoimpactontheoutcomeofthenext
toss.

Eachtossisanindependentevent,justlikethedistributionofallelesintogametes.
Likeacointoss,eachovumfromaheterozygousparenthasa1/2chanceofcarryingthe
dominantalleleanda1/2chanceofcarryingtherecessiveallele.
Thesameoddsapplytothesperm.
IG Lecture Outline 14-5

Wecanusethemultiplicationruletodeterminethechancethattwoormoreindependent
eventswilloccurtogetherinsomespecificcombination.
Computetheprobabilityofeachindependentevent.
Multiplytheindividualprobabilitiestoobtaintheoverallprobabilityoftheseevents
occurringtogether.
Theprobabilitythattwocoinstossedatthesametimewilllandheadsupis1/21/2=
1/4.
Similarly,theprobabilitythataheterozygouspeaplant(Pp)willselffertilizetoproduce
awhitefloweredoffspring(pp)isthechancethataspermwithawhiteallelewillfertilize
anovumwithawhiteallele.
Thisprobabilityis1/21/2=1/4.

Theruleofmultiplicationalsoappliestodihybridcrosses.
Foraheterozygousparent(YyRr)theprobabilityofproducingaYRgameteis1/21/2=
1/4.
WecanusethistopredicttheprobabilityofaparticularF 2genotypewithoutconstructing
a16partPunnettsquare.
TheprobabilitythatanF2plantfromheterozygousparentswillhaveaYYRRgenotypeis
1/16(1/4chanceforaYRovumand1/4chanceforaYRsperm).
Theruleofadditionalsoappliestogeneticproblems.

Undertheruleofaddition,theprobabilityofaneventthatcanoccurtwoormore
differentwaysisthesumoftheseparateprobabilitiesofthoseways.
Forexample,therearetwowaysthatF1gametescancombinetoformaheterozygote.
Thedominantallelecouldcomefromthespermandtherecessivefromtheovum
(probability=1/4).
Orthedominantallelecouldcomefromtheovumandtherecessivefromthesperm
(probability=1/4).
Theprobabilityofobtainingaheterozygoteis1/4+1/4=1/2.
Wecancombinetherulesofmultiplicationandadditiontosolvecomplexproblemsin
Mendeliangenetics.
Letsdeterminetheprobabilityofanoffspringhavingtworecessivephenotypesforat
leasttwoofthreetraitsresultingfromatrihybridcrossbetweenpeaplantsthatarePpYyRr
andPpyyrr.
Therearefivepossiblegenotypesthatfulfillthiscondition:ppyyRr,ppYyrr,Ppyyrr,
PPyyrr,andppyyrr.
Wecanusetheruleofmultiplicationtocalculatetheprobabilityforeachofthese
genotypesandthenusetheruleofadditiontopooltheprobabilitiesforfulfillingthe
conditionofatleasttworecessivetraits.

TheprobabilityofproducingappyyRroffspring:
Theprobabilityofproducingpp=1/21/2=1/4.
Theprobabilityofproducingyy=1/21=1/2.
TheprobabilityofproducingRr=1/21=1/2.
Therefore,theprobabilityofallthreebeingpresent(ppyyRr)inoneoffspringis1/41/2
1/2=1/16.

ForppYyrr:1/41/21/2=1/16.

ForPpyyrr:1/21/21/2=1/8or2/16.
IG Lecture Outline 14-6

ForPPyyrr:1/41/21/2=1/16.

Forppyyrr:1/41/21/2=1/16.

Therefore,thechancethatagivenoffspringwillhaveatleasttworecessivetraitsis1/16
+2/16+1/16+1/16=6/16.
5.Mendeldiscoveredtheparticulatebehaviorofgenes:areview.
Whilewecannotpredictwithcertaintythegenotypeorphenotypeofanyparticularseed
fromtheF2generationofadihybridcross,wecanpredicttheprobabilitythatitwillhavea
specificgenotypeorphenotype.
Mendelsexperimentssucceededbecausehecountedsomanyoffspring,wasableto
discernthestatisticalnatureofinheritance,andhadakeensenseoftherulesofchance.
Mendelslawsofindependentassortmentandsegregationexplainheritablevariationin
termsofalternativeformsofgenesthatarepassedalongaccordingtosimplerulesof
probability.
Theselawsapplynotjusttogardenpeas,buttoalldiploidorganismsthatreproduceby
sexualreproduction.
Mendelsstudiesofpeainheritanceendurenotonlyingenetics,butasacasestudyofthe
powerofscientificreasoningusingthehypotheticodeductiveapproach.
B.ExtendingMendelianGenetics
1.Therelationshipbetweengenotypeandphenotypeisrarelysimple.
Inthe20thcentury,geneticistshaveextendedMendelianprinciplesnotonlytodiverse
organisms,butalsotopatternsofinheritancemorecomplexthanMendeldescribed.
Infact,Mendelhadthegoodfortunetochooseasystemthatwasrelativelysimple
genetically.
EachcharacterthatMendelstudiediscontrolledbyasinglegene.
Eachgenehasonlytwoalleles,oneofwhichiscompletelydominanttotheother.
TheheterozygousF1offspringofMendelscrossesalwayslookedlikeoneoftheparental
varietiesbecauseoneallelewasdominanttotheother.

Therelationshipbetweengenotypeandphenotypeisrarelysosimple.

Theinheritanceofcharactersdeterminedbyasinglegenedeviatesfromsimple
Mendelianpatternswhenallelesarenotcompletelydominantorrecessive,whenagenehas
morethantwoalleles,orwhenageneproducesmultiplephenotypes.

Wewillconsiderexamplesofeachofthesesituations.

Allelesshowdifferentdegreesofdominanceandrecessivenessinrelationtoeachother.

OneextremeisthecompletedominancecharacteristicofMendelscrosses.

Attheotherextremefromcompletedominanceiscodominance,inwhichtwoalleles
affectthephenotypeinseparate,distinguishableways.
Forexample,theM,N,andMNbloodgroupsofhumansareduetothepresenceoftwo
specificmoleculesonthesurfaceofredbloodcells.
PeopleofgroupM(genotypeMM)haveonetypeofmoleculeontheirredbloodcells,
peopleofgroupN(genotypeNN)havetheothertype,andpeopleofgroupMN
(genotypeMN)havebothmoleculespresent.
IG Lecture Outline 14-7

TheMNphenotypeisnotintermediatebetweenMandNphenotypesbutratherexhibits
boththeMandtheNphenotype.

Someallelesshowincompletedominance,inwhichheterozygotesshowadistinct
intermediatephenotypenotseeninhomozygotes.
Thisisnotblendinginheritancebecausethetraitsareseparable(particulate),asshownin
furthercrosses.
Offspringofacrossbetweenheterozygotesshowthreephenotypes:eachparentalandthe
heterozygote.
Thephenotypicandgenotypicratiosareidentical:1:2:1.

Aclearexampleofincompletedominanceisseeninflowercolorofsnapdragons.
AcrossbetweenawhitefloweredplantandaredfloweredplantwillproduceallpinkF 1
offspring.
SelfpollinationoftheF1offspringproduces25%white,25%red,and50%pinkF2
offspring.

Therelativeeffectsoftwoallelesrangefromcompletedominanceofoneallele,through
incompletedominanceofeitherallele,tocodominanceofbothalleles.
Itisimportanttorecognizethatadominantalleledoesnotsomehowsubduearecessive
allele.

Allelesaresimplyvariationsinagenesnucleotidesequence.
Whenadominantallelecoexistswitharecessivealleleinaheterozygote,theydonot
interactatall.

Toillustratetherelationshipbetweendominanceandphenotype,letusconsiderMendels
characterofroundversuswrinkledpeaseedshape.
Peaplantswithwrinkledseedshavetwocopiesoftherecessiveallele.
Theseedsarewrinkledduetotheaccumulationofmonosaccharidesbecauseofthelack
ofakeyenzymethatconvertsthemtostarch.
Excesswaterenterstheseedduetotheaccumulationofmonosaccharides.
Theseedswrinklewhentheexcesswaterdries.
Bothhomozygousdominantsandheterozygotesproduceenoughenzymestoconvertall
themonosaccharidesintostarch.
Asaresult,theydonotfillwithexcesswaterandformsmoothseedsastheydry.
Foranycharacter,dominance/recessivenessrelationshipsdependonthelevelatwhich
weexaminethephenotype.
Forexample,humanswithTaySachsdiseaselackafunctioningenzymetometabolize
certainlipids.Theselipidsaccumulateinthebrain,harmingbraincells,andultimately
leadingtodeath.
ChildrenwithtwoTaySachsalleles(homozygotes)havethedisease.
Bothheterozygoteswithoneworkingalleleandhomozygoteswithtwoworkingalleles
arehealthyandnormalattheorganismallevel.
Theactivitylevelofthelipidmetabolizingenzymeisreducedinheterozygotes.Atthe
biochemicallevel,theallelesshowincompletedominance.
Heterozygousindividualsproduceequalnumbersofnormalanddysfunctionalenzyme
molecules.Atthemolecularlevel,theTaySachsandfunctionalallelesarecodominant.
Adominantalleleisnotnecessarilymorecommoninapopulationthantherecessive
allele.
IG Lecture Outline 14-8

Forexample,onebabyin400isbornwithpolydactyly,aconditioninwhichindividuals
arebornwithextrafingersortoes.
Polydactylyisduetoadominantallele.
However,therecessivealleleisfarmoreprevalentthanthedominantallele.
399individualsoutof400havefivedigitsperappendage.

Manygenesexistinpopulationsinmorethantwoallelicforms.

TheABObloodgroupsinhumansaredeterminedbythreealleles,IA,IB,andi.
BoththeIAandIBallelesaredominanttotheiallele.
TheIAandIBallelesarecodominanttoeachother.

Becauseeachindividualcarriestwoalleles,therearesixpossiblegenotypesandfour
possiblebloodtypes.
IndividualsthatareIAIAorIAiaretypeAandhavetypeAcarbohydratesonthesurfaceof
theirredbloodcells.
IndividualsthatareIBIBorIBiaretypeBandhavetypeBcarbohydratesonthesurfaceof
theirredbloodcells.
IndividualsthatareIAIBaretypeABandhavebothtypeAandtypeBcarbohydrateson
thesurfaceoftheirredbloodcells.
IndividualsthatareiiaretypeOandhaveneithercarbohydrateonthesurfaceoftheirred
bloodcells.
Matchingcompatiblebloodgroupsiscriticalforbloodtransfusionsbecauseaperson
producesantibodiesagainstforeignbloodfactors.
IfthedonorsbloodhasanAorBcarbohydratethatisforeigntotherecipient,antibodies
intherecipientsbloodwillbindtotheforeignmolecules,causethedonatedbloodcells
toclumptogether,andcankilltherecipient.

Thegenesthatwehavecoveredsofaraffectonlyonephenotypiccharacter.

However,mostgenesarepleiotropic,affectingmorethanonephenotypiccharacter.
Forexample,thewiderangingsymptomsofsicklecelldiseaseareduetoasinglegene.

Consideringtheintricatemolecularandcellularinteractionsresponsibleforan
organismsdevelopment,itisnotsurprisingthatagenecanaffectanumberof
characteristics.
Inepistasis,ageneatonelocusaltersthephenotypicexpressionofageneatasecond
locus.
Forexample,inmiceandmanyothermammals,coatcolordependsontwogenes.
One,theepistaticgene,determineswhetherpigmentwillbedepositedinhairornot.
Presence(C)isdominanttoabsence(c)ofpigment.
Thesecondgenedetermineswhetherthepigmenttobedepositedisblack(B)orbrown
(b).
Theblackalleleisdominanttothebrownallele.
Anindividualthatiscchasawhite(albino)coatregardlessofthegenotypeofthesecond
gene.
Acrossbetweentwoblackmicethatareheterozygous(BbCc)willfollowthelawof
independentassortment.
However,unlikethe9:3:3:1offspringratioofanormalMendelianexperiment,the
offspringratioisnineblack,threebrown,andfourwhite.
IG Lecture Outline 14-9

Allccmicewillbealbino,regardlessoftheallelestheyinheritattheBgene.

Somecharacterscannotbeclassifiedaseitheror,asMendelsgeneswere.

Quantitativecharactersvaryinapopulationalongacontinuum.

Theseareusuallyduetopolygenicinheritance,theadditiveeffectsoftwoormoregenes
onasinglephenotypiccharacter.
Forexample,skincolorinhumansiscontrolledbyatleastthreeindependentgenes.
Imaginethateachgenehastwoalleles,onelightandonedark,whichdemonstrate
incompletedominance.
AnAABBCCindividualisverydark;anaabbccindividualisverylight.
AcrossbetweentwoAaBbCcindividuals(withintermediateskinshade)willproduce
offspringcoveringawiderangeofshades.
Individualswithintermediateskinshadeswillbemostcommon,butsomeverylightand
verydarkindividualscouldbeproducedaswell.
Therangeofphenotypeswillformanormaldistribution,ifthenumberofoffspringis
greatenough.

Phenotypedependsonenvironmentandgenes.
Apersonbecomesdarkeriftheytan,despitetheirinheritedskincolor.
Asingletreemayhaveleavesthatvaryinsize,shape,andgreenness,dependingon
exposuretowindandsun.
Forhumans,nutritioninfluencesheight,exercisealtersbuild,suntanningdarkensskin,
andexperienceimprovesperformanceonintelligencetests.
Evenidenticaltwins,whoaregeneticallyidentical,accumulatephenotypicdifferencesas
aresultoftheiruniqueexperiences.

Therelativeimportanceofgenesandtheenvironmentininfluencinghuman
characteristicsisaveryoldandhotlycontesteddebate.
Theproductofagenotypeisgenerallynotarigidlydefinedphenotype,butarangeof
phenotypicpossibilities,thenormofreaction,thataredeterminedbytheenvironment.
Insomecases,thenormofreactionhasnobreadth,andagivengenotypespecifiesa
particularphenotype(forexample,bloodtype).
Incontrast,apersonsredandwhitebloodcellcountvarieswithfactorssuchasaltitude,
customaryexerciselevel,andpresenceofinfection.

Normsofreactionarebroadestforpolygeniccharacters.
Forthesemultifactorialcharacters,environmentcontributestotheirquantitativenature.

Areductionistemphasisonsinglegenesandsinglephenotypiccharacterspresentsan
inadequateperspectiveonheredityandvariation.

AmorecomprehensivetheoryofMendeliangeneticsmustvieworganismsasawhole.

Thetermphenotypecanrefernotonlytospecificcharacterssuchasflowercolororblood
group,butalsotoanorganisminitsentirety,includingallaspectsofitsphysicalappearance.
Genotypecanrefernotjusttoasinglegeneticlocus,butalsotoanorganismsentire
geneticmakeup.
Anorganismsphenotypereflectsitsoverallgenotypeanditsuniqueenvironmental
history.
C.MendelianInheritanceinHumans
IG Lecture Outline 14-10

Whilepeasareconvenientsubjectsforgeneticresearch,humansarenot.
Thegenerationtimeistoolong,fecundityistoolow,andbreedingexperimentsare
unacceptable.

Yethumansaresubjecttothesamerulesgoverninginheritanceasotherorganisms.

Newtechniquesinmolecularbiologyhaveledtomanybreakthroughdiscoveriesinthe
studyofhumangenetics.
1.PedigreeanalysisrevealsMendelianpatternsinhumaninheritance.
Ratherthanmanipulatematingpatternsofpeople,geneticistsanalyzetheresultsof
matingsthathavealreadyoccurred.
Inapedigreeanalysis,informationaboutthepresenceorabsenceofaparticular
phenotypictraitiscollectedfromasmanyindividualsinafamilyaspossible,across
generations.

Thedistributionofthesecharactersisthenmappedonthefamilytree.
Forexample,theoccurrenceofwidowspeak(W)isdominanttoastraighthairline(w).
Phenotypesoffamilymembersandknowledgeofdominant/recessiverelationsbetween
allelesallowresearcherstopredictthegenotypesofmembersofthisfamily.
Forexample,ifanindividualinthethirdgenerationlacksawidowspeak,butbothher
parentshavewidowspeaks,thenherparentsmustbeheterozygousforthatgene.
Ifsomesiblingsinthesecondgenerationlackawidowspeakandoneofthe
grandparents(firstgeneration)alsolacksone,thenweknowtheothergrandparentmust
beheterozygous,andwecandeterminethegenotypeofmanyotherindividuals.

Wecanusethesamefamilytreetotracethedistributionofattachedearlobes(f),a
recessivecharacteristic.

Individualswithadominantallele(F)havefreeearlobes.

Someindividualsmaybeambiguous,especiallyiftheyhavethedominantphenotypeand
couldbeheterozygousorhomozygousdominant.

Apedigreecanhelpusunderstandthepastandpredictthefuture.

WecanusenormalMendelianrules,includingmultiplicationandaddition,topredictthe
probabilityofspecificphenotypes.
Forexample,theserulescouldbeusedtopredicttheprobabilitythatachildwithWwFf
parentswillhaveawidowspeakandattachedearlobes.
Thechanceofhavingawidowspeakis3/4(1/2[WW]+1/4[Ww]).
Thechanceofhavingattachedearlobesis1/4[ff].
Thiscombinationhasaprobabilityof3/41/4=3/16.
2.ManyhumandisordersfollowMendelianpatternsofinheritance.
Thousandsofgeneticdisorders,includingdisablingordeadlyhereditarydiseases,are
inheritedassimplerecessivetraits.
Theseconditionsrangefromrelativelymild(albinism)tolifethreatening(cystic
fibrosis).
Therecessivebehavioroftheallelescausingtheseconditionsoccursbecausetheallele
codesforamalfunctioningproteinorfornoproteinatall.
Heterozygoteshaveanormalphenotypebecauseonenormalalleleproducesenoughof
therequiredprotein.
IG Lecture Outline 14-11

Arecessivelyinheriteddisordershowsuponlyinhomozygousindividualswhoinherita
recessiveallelefromeachparent.

Individualswholackthedisorderareeitherhomozygousdominantorheterozygotes.

Whileheterozygotesmaylackobviousphenotypiceffects,theyarecarrierswhomay
transmitarecessivealleletotheiroffspring.

Mostpeoplewithrecessivedisordersareborntocarrierswithnormalphenotypes.
Twocarriershavea1/4chanceofhavingachildwiththedisorder,1/2chanceofhaving
achildwhoisacarrier,and1/4chanceofhavingachildwithoutadefectiveallele.

Geneticdisordersarenotevenlydistributedamongallgroupsofhumans.

Thisresultsfromthedifferentgenetichistoriesoftheworldspeopleduringtimeswhen
populationsweremoregeographicallyandgeneticallyisolated.

Cysticfibrosisstrikesoneofevery2,500whitesofEuropeandescent.
Onein25peopleofEuropeandescentisacarrierforthiscondition.
ThenormalalleleforthisgenecodesforamembraneproteinthattransportsCl between
cellsandextracellularfluid.
Ifthesechannelsaredefectiveorabsent,thereareabnormallyhighextracellularlevelsof
chloride.
Thiscausesthemucuscoatsofcertaincellstobecomethickerandstickierthannormal.
Thismucusbuildupinthepancreas,lungs,digestivetract,andelsewherecausespoor
absorptionofnutrients,chronicbronchitis,andbacterialinfections.
Withouttreatment,affectedchildrendiebeforefive,butwithtreatment,theycanlivepast
theirlate20soreven30s.
TaySachsdiseaseisanotherlethalrecessivedisorder.
Itiscausedbyadysfunctionalenzymethatfailstobreakdownspecificbrainlipids.
Thesymptomsbeginwithseizures,blindness,anddegenerationofmotorandmental
performanceafewmonthsafterbirth.
Inevitably,thechilddiesafterafewyears.
AmongAshkenazicJews(thosefromcentralEurope),thisdiseaseoccursinoneof3,600
births,about100timesgreaterthantheincidenceamongnonJewsorMediterranean
(Sephardic)Jews.

ThemostcommoninheriteddiseaseamongpeopleofAfricandescentissicklecell
disease,whichaffectsoneof400AfricanAmericans.
Sicklecelldiseaseiscausedbythesubstitutionofasingleaminoacidinhemoglobin.
Whenoxygenlevelsinthebloodofanaffectedindividualarelow,sicklecell
hemoglobinaggregateintolongrodsthatdeformredbloodcellsintoasickleshape.
Thissicklingcreatesacascadeofsymptoms,demonstratingthepleiotropiceffectsofthis
allele,assickledcellsclumpandclogcapillariesthroughoutthebody.
Doctorscanuseregularbloodtransfusionstopreventbraindamageandnewdrugsto
preventortreatotherproblems.
Attheorganismallevel,thenonsicklealleleisincompletelydominanttothesicklecell
allele.
Carriersaresaidtohavesicklecelltrait.
Theseindividualsareusuallyhealthy,althoughsomesuffersomesymptomsofsicklecell
diseaseunderbloodoxygenstress.
IG Lecture Outline 14-12

Atthemolecularlevel,thetwoallelesarecodominantasbothnormalandabnormal
(sicklecell)hemoglobinsaresynthesized.

AboutoneintenAfricanAmericanshassicklecelltrait.
Thehighfrequencyofheterozygotesisunusualforanallelewithseveredetrimental
effectsinhomozygotes.
Individualswithonesicklecellallelehaveincreasedresistancetomalaria,aparasitethat
spendspartofitslifecycleinredbloodcells.
IntropicalAfrica,wheremalariaiscommon,thesicklecellalleleisbothaboonanda
bane.
Homozygousnormalindividualsdieofmalariaandhomozygousrecessive
individualsdieofsicklecelldisease,whilecarriersarerelativelyfreeofboth.

TherelativelyhighfrequencyofsicklecelltraitinAfricanAmericansisavestigeof
theirAfricanroots.
Normallyitisrelativelyunlikelythattwocarriersofthesamerare,harmfulallelewill
meetandmate.

However,consanguineousmatingsbetweencloserelativesincreasetherisk.
Individualswhosharearecentcommonancestoraremorelikelytocarrythesame
recessivealleles.

Mostsocietiesandcultureshavelawsortaboosforbiddingmarriagesbetweenclose
relatives.
Althoughmostharmfulallelesarerecessive,anumberofhumandisordersaredueto
dominantalleles.
Forexample,achondroplasia,aformofdwarfism,hasanincidenceofonecasein25,000
people.
Heterozygousindividualshavethedwarfphenotype.
Thosewhoarenotachondroplasticdwarfs,99.99%ofthepopulation,arehomozygous
recessiveforthistrait.
Thisprovidesanotherexampleofatraitforwhichtherecessivealleleisfarmore
prevalentthanthedominantallele.

Lethaldominantallelesaremuchlesscommonthanlethalrecessives.
Ifalethaldominantkillsanoffspringbeforeitcanmatureandreproduce,theallelewill
notbepassedontofuturegenerations.
Incontrast,alethalrecessiveallelecanbepassedonbyheterozygouscarrierswhohave
normalphenotypes.

Alethaldominantallelecanescapeeliminationifitcausesdeathatarelativelyadvanced
age,aftertheindividualhasalreadypassedonthelethalalleletohisorherchildren.

OneexampleisHuntingtonsdisease,adegenerativediseaseofthenervoussystem.
Thedominantlethalallelehasnoobviousphenotypiceffectuntilanindividualisabout
35to45yearsold.
Thedeteriorationofthenervoussystemisirreversibleandinevitablyfatal.

AnychildborntoaparentwhohasthealleleforHuntingtonsdiseasehasa50%chance
ofinheritingthediseaseandthedisorder.

IntheUnitedStates,thisdevastatingdiseaseafflictsonein10,000people.

IG Lecture Outline 14-13

Recently,moleculargeneticistshaveusedpedigreeanalysisofaffectedfamiliestotrack
theHuntingtonsalleletoalocusnearthetipofchromosome4.
ThishasledtothedevelopmentofatestthatcandetectthepresenceoftheHuntingtons
alleleinanindividualsgenome.
WhilesomediseasesareinheritedinasimpleMendelianfashionduetoallelesatasingle
locus,manyotherdisordershaveamultifactorialbasis.
Thesemayhaveageneticcomponentplusasignificantenvironmentalinfluence.
Multifactorialdisordersincludeheartdisease;diabetes;cancer;alcoholism;andcertain
mentalillnesses,suchasschizophreniaandmanicdepressivedisorder.
Thegeneticcomponentofsuchdisordersistypicallypolygenic.
Atpresent,littleisunderstoodaboutthegeneticcontributiontomostmultifactorial
diseases.
Thebestpublichealthstrategyiseducationaboutrelevantenvironmentalfactorsand
promotionofhealthybehavior.
3.Technologyisprovidingnewtoolsforgenetictestingandcounseling.

ApreventiveapproachtosimpleMendeliandisordersissometimespossible.

Theriskthataparticulargeneticdisorderwilloccurcansometimesbeassessedbeforea
childisconceivedorearlyinpregnancy.
Manyhospitalshavegeneticcounselorstoprovideinformationtoprospectiveparents
whoareconcernedaboutafamilyhistoryofaspecificdisease.
Considerahypotheticalcouple,JohnandCarol,whoareplanningtohavetheirfirst
child.
Inbothoftheirfamilieshistories,arecessivelethaldisorderispresent.BothJohnand
Carolhadbrotherswhodiedofthedisease.
WhilenotoneofJohn,Carol,ortheirparentshavethedisease,theirparentsmusthave
beencarriers(AaAa).
JohnandCaroleachhavea2/3chanceofbeingcarriersanda1/3chanceofbeing
homozygousdominant.
Theprobabilitythattheirfirstchildwillhavethediseaseis2/3(chancethatJohnisa
carrier)2/3(chancethatCarolisacarrier)1/4(chancethattheoffspringoftwo
carriersishomozygousrecessive)=1/9.
Iftheirfirstchildisbornwiththedisease,weknowthatJohnandCarolsgenotypemust
beAaandtheyarebothcarriers.
Inthatcase,thechancethattheirnextchildwillalsohavethediseaseis1/4.

Mendelslawsaresimplytherulesofprobabilityappliedtoheredity.
Becausechancehasnomemory,thegenotypeofeachchildisunaffectedbythe
genotypesofoldersiblings.
ThechancethatJohnandCarolsfirstthreechildrenwillhavethedisorderis1/41/4
1/4=1/64.Shouldthatoutcomehappen,thelikelihoodthatafourthchildwillalsohave
thedisorderisstill1/4.

Becausemostchildrenwithrecessivedisordersareborntoparentswithanormal
phenotype,thekeytoassessingriskisidentifyingwhetherprospectiveparentsarecarriersof
therecessivetrait.
Recentlydevelopedtestsforseveraldisorderscandistinguishnormalphenotypesin
heterozygotesfromhomozygousdominants.
IG Lecture Outline 14-14

Theseresultsallowindividualswithafamilyhistoryofageneticdisordertomake
informeddecisionsabouthavingchildren.
However,issuesofconfidentiality,discrimination,andcounselingmayarise.

Testsarealsoavailabletodetermineinuteroifachildhasaparticulardisorder.

Onetechnique,amniocentesis,canbeusedfromthe14thto16thweekofpregnancyto
assesswhetherthefetushasaspecificdisease.
Fetalcellsextractedfromamnioticfluidareculturedandkaryotypedtoidentifysome
disorders.
Otherdisorderscanbeidentifiedfromchemicalsintheamnioticfluids.
Asecondtechnique,chorionicvillussampling(CVS)allowsfasterkaryotypingandcan
beperformedasearlyastheeighthtotenthweekofpregnancy.
Thistechniqueextractsasampleoffetaltissuefromthechorionicvillioftheplacenta.
Thistechniqueisnotsuitablefortestsrequiringamnioticfluid.
Othertechniques,ultrasoundandfetoscopy,allowfetalhealthtobeassessedvisuallyin
utero.
Bothfetoscopyandamniocentesiscausecomplicationssuchasmaternalbleedingorfetal
deathinabout1%ofcases.
Therefore,thesetechniquesareusuallyreservedforcasesinwhichtheriskofagenetic
disorderorothertypeofbirthdefectisrelativelygreat.
Iffetaltestsrevealaseriousdisorder,theparentsfacethedifficultchoiceofterminating
thepregnancyorpreparingtocareforachildwithageneticdisorder.
Somegenetictraitscanbedetectedatbirthbysimpleteststhatarenowroutinely
performedinhospitals.
Onetestcandetectthepresenceofarecessivelyinheriteddisorder,phenylketonuria
(PKU).
Thisdisorderoccursinonein10,000to15,000births.
Individualswiththisdisorderaccumulatetheaminoacidphenylalanineanditsderivative
phenylpyruvateinthebloodtotoxiclevels.
Thisleadstomentalretardation.
Ifthedisorderisdetected,aspecialdietlowinphenylalanineusuallypromotesnormal
development.
Unfortunately,fewothergeneticdiseasesaresotreatable.

IG Lecture Outline 14-15

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