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Test Bank For Human Genetics, 13th Edition All Chapters
b b b b b b b b b



-



Lectureb1:b-bbbANSWERbb

-bDNAbisbpackagedbasbchromatin,bchromosomesbbecomebvisiblebduringbmitosis.b-
bbbANSWERbb




Homologues-b(maternalbandbpaternalbformsbofbsamebchromosome)b-bbbANSWERbb

Meiosis:bG1,bS,bG2,bM.bBeforebreplicationbphase,bchromosomesbhavebonebchromatidba
ndbafterbreplication,bchromosomesbhaveb2bsisterbchromatids,bheldbtogetherbatbthebcentr
omere.bEndsbwithb4bdaughterbcellsbwithb1bchromatidbeach.b-bbbANSWERbb

Keybdifferencesbfrombmitosis:bHomologsbpairb(ProphasebI),bSisterbcentromeresbactbasba
bsinglebcentromereb(MetaphasebI),bSisterbchromatidsbremainbattachedb(AnaphasebI),bM

eiosisbIbisbabreductionbdivision-
bmeaningbstartbmeiosisbIbwithb46bunitsbandbendbmeiosisbIbwithb23bunitsb(b2bchromatidsbinb

eachbhaploidbdaughterbcells),bMeiosisbIIbisbanbequationalbdivisionb(identicalbtobmitosis).b-
bbbANSWERbb




RecombinationboccursbinbProphasebI.bCrossingboverbandbrecombbisbExchangebofbhomo
logousbsegmentsbbetweenbnon-sisterbchromatids.b-bbbANSWERbb

HomologuesbmovebapartbduringbanaphasebI-
disjunction.b223bpossiblebcombinationsbofbchromosomes.bInbcytokinesisbI,bCellsbdividebi
ntobtwobhaploidbdaughterbcells.bOnebcellbreceivesbmostbofbthebcytoplasmbandbthebotherb
becomesbthebfirstbpolarbbodybwhichbdoesn'tbgobthroughbMeiosisbII.bMeiosisbIbendsbafterb
ovulation.bNonbdysjunctionbinbmeiosisbI:bcanbcausebproblemsblikebTrisomyb21.b-
bbbANSWERbb




-
Briefbinterphasebbetweenbfirstbandbsecondbmeioticbdivisions.bNobSbphaseboccursbinbMei
osisbII.b-bbbANSWERbb

-
Inbthebsecondbmeioticbdivisionbabsecondbpolarbbodybformsbduringboogenesis.bInboogene
sis,beggbisbarrestedbinbmetaphasebIIbuntilbfertilization.b-bbbANSWERbb

AfterbMeiosisbtherebisbabReductionbofbchromosomebnumberb2nn.b(diploidbvs.bhaploidbcel
ls)-
bNotationb'n'bhasbtobdobwithbamountbofbDNAb(#of bnucleotides),bnotbthebnecessarilybtheb#b

ofbchromosomes.b-bbbANSWERbb

,Lectureb2:bPatternsbofbInheritanceb-bbbANSWERbb

MedelianbInheritance-
bdeterminedbbybabsingle bmajorbgene.bBasedbonbindependentbassortment.bDihybridbcros

sb(2bgenotypes)bwithbry,bRy,brY,bRybsetbupbonbbothbsidesphenotypicbratiobofb9:3:3:1-
yellowbround,bgreenbround,byellowbwrinkled,bgreenbwrinkled,bIfbgetb9:3:3:1byoubknowbtha
tbsegregationbisbindependent.b-bbbANSWERbb

Multifactorialbinheritance-multiplebgeneticbandbnon-geneticbfactorsbinvolvedb-
bbbANSWERbb




Compoundbheterozygous:bhasbtwobdifferentbmutantballelesbforbabcharacterb-
bbbANSWERbb




Linkage-
2bgenesbphysicallybnearbeachbotherbonbabchromosomebwillbnotbassortbrandomlybinbmeio
sis.bTightlyblinked:bwillbgetb2btypesbofbgametesbex.bPLbandbpl.bUnlinked:bwillbgetb4btypesb
ofbgametesbPL,bPl,bpL,bpl.b-bbbANSWERbb

Thebfrequencybofbrecombinationbbetweenbtwobgenesbisbproportionalbtobthebdistancebbet
weenbthebgenes.bThebcloserbthebgenesbarebonbthebchromosomebtheblessblikelybcrossingb
overboccurs.bLinkagebmap:b1%brecombinationb=b1bmapbunitb=b1bcentiMorganb(cM),bMap
bdistancesbarebadditive.b-bbbANSWERbb




Thebnon-
randombassociationbbetweenballelesbatbtwoblocationsbonbabchromosomebisbcalledblinkag
ebdisequilibrium.bIfbthebfrequencybofbchromosomesbwithbAB=Ab=aB=abbthenbthebgenes
barebinbequilibrium.bIfbfrequencybofb1ballelebisbseenbmoreb(AbmorebthanbBbforbex)bthenbge

nesbarebinblinkagebdisequilibrium.b-bbbANSWERbb

AutosomalbdominantbinheritancebExamples:b-bbbANSWERbb

Achondroplasia-
bFGFR3bmutations,bAlwaysbfullbpenetrancebwithbachondroplasiab(sobnormalbparentsbha

vebabchildbwithbaplasiabthenbit'sbabnewbmutation).bHeterozygousbb/cbhomozygotesbusual
lybdiebinbuterob-bbbANSWERbb

Neurofibromatosis-bNF1b(neurofibromin)bandbNF2b(merlin)bmutations.b-bbbANSWERbb

Incompletebdominance-
bmixedbphenotype.bInbcasesbofbdisease,bDominantbdisordersbarebmorebseverebinbhomoz

ygotesbthenbinbheterozygotesb(termedbalsob"semidominant")bIe.bFamilialbHypercholeste
rolemia.b-bbbANSWERbb

Co-dominance-
bphenotypicbexpressionbofbtwobdifferentballelesbforbablocusbie.bBloodbtype.b-bbbANSWERbb




Autosomalbrecessivebinheritance:bExamples:bCysticbfibrosis,bTay-
Sachsbdisease,bSickle-cellbdiseaseb-bbbANSWERbb

,Pseudodominance:bthebinheritancebofbanbautosomalbrecessivebtraitbmimicsbanbautoso
malbdominantbpatternb-bbbANSWERbb

MalesbarebhemizygousbwithbrespectbtobX-linkedbgenes.b-bbbANSWERbb

X-
linkedbdominantbinheritance:bAffectedbfemalesbarebtwicebasbcommonbasbaffectedbmales
bbutbmalesbusuallybmorebseverelybaffectedborbthebdisorderbmaybbeblethalbinbmalesb(Rettb

syndrome).b-bbbANSWERbb

X-
linkedbrecessive:bincidencebisbmuchbhigherbinbmalesbandbaffectedbmalesbdobnotbusuallyb
transmitbthebdisorderbunlessbmotherbisbabcarrier.bHeterozygotebfemalesbarebusuallybuna
ffected,bbutbsomebmaybexpressbthebconditionbwithbvariablebseveritybasbdeterminedbbybth
ebpatternbofbXbinactivation.bAbsignificantbproportionbofbisolatedbcasesbarebduebtobnewbmu
tationb(Duchennebmuscularbdystrophy-DMD).b-bbbANSWERbb

Pseudoautosomalbinheritance-
bgroupbofbgenesbonbthebinactivebxbchromosomebarebNOTbinactivated.bDiseasesbassocia

tedbwithbthesebgenesbarebinheritedbsimilarbtobautosomalbinheritance.b-bbbANSWERbb

SamebamountbofbX-
linkedbgenebproductsbbetweenbmalesbandbfemalesbachievedbthroughbdosagebcompens
ation.bLyonbHypothesisbstatesbthatbthebinactivebXbisbNOTbrandomlybchosenbinbeachbcellb
Ex.bAbstructurallybabnormalbXbisbpreferentiallybinactivated.bInactivationbisbNOTbcomplet
e-
bsomebgenesbcanbescapebinactivationb(ie.bThosebwithbabfunctionalbhomologbonbthebY).bI

nactivationbisbNOTbpermanent-
breversedbinbdevelopmentbofbgermbcellsb(notbpassedbonbtobgametes).b-bbbANSWERbb




ThebkeybplayerbisbthebX-
linkedbgenebXIST→bXb(inactive)bspecificbtranscript.bXISTbisbtranscribedbtobproducebabno
n-codingbRNAbthatb"coats"bthebX-
chromosomebandbinactivatesbit.bXISTbisbonlybexpressedbfrombthebinactivebX.bThebhiston
esbonbthebcoatedbXbundergobmethylationbwhichbcausesbthebchromosomebtobcondenseb(
heterochromatin),bformingbabBarrbbody.b-bbbANSWERbb

-
SomebgenesbdobnotbhavebYbhomologuebandbdobnotbundergobinactivationb(e.g.bsteroidbs
ulfatasebgene)b-bbbANSWERbb

-Random/skewedbinactivationbmaybresultbinbaffected/totallybhealthybheterozygotes.b-
bbbANSWERbb




VariablebexpressionbofbX-
inactivation:bOnbbothbextremes,babheterozygousbfemalebwithbrecessivebx-
linkedbdiseasebcouldbmanifestbthebdisease.bInbabcasebwithbabdominantbX-
linkedbtrait,binbwhichbalmostballbofbabfemalesbXbchromosomesbwithbmutationbisbinactive,b
mightbnotbmanifestbthisbdisease.bIdenticalbtwinsbcouldbevenbhavebdiffbphenotypesbduebt
obskewedbXbinactivation.b-bbbANSWERbb

, Mosaicism-
bXbchromosomebinactivationboccursbrandomlybandbinactivationbpatternbisbpassedbtobcellb

progeny.bResult:bfunctionalbmosaicismbinbwhichbfemalebisbabmosaicbwithbrespectbtobexp
ressionbofbgenesbonbXbchrom.bEx.bCalicobCat,bBb-bdominantborange,bbb-
brecessivebgenebblack,bGenesbforbwhite:bautosomal.b-bbbANSWERbb




GeneticbHeterogeneitybcanbbebthebresultbofbLocusbHeterogeneityb,bAllelicbHeterogeneit
y,bandbModifierbLoci.b-bbbANSWERbb

LocusbHeterogeneity-
babsinglebdisorder,btrait,borbpatternbofbtraitsbcausedbbybmutationsbinbgenesbatbdifferentbch

romosomalbloci.bEx.bretinitisbpigmentosabhasbautosomalbdominant,bautosomalbrecessiv
e,bandbX-
linkedborigins.bHowever,bonlybonebmutantblocusbisbneededbforbthebphenotypebtobmanifes
tb-bbbANSWERbb

Allelicbheterogeneityb-
bManybgeneticblocibpossessbmorebthanbonebmutantballele.bInbthebCFTRbgene,bnearlyb14

00bmutationsbfound.bSomebmutationsbcausebclassicalbCFb+bpancreaticbinsufficiencyb+bc
ongenitalbabsencebofbvasbdeferens,bothersbcauseblungbdiseasebwithbnormalbpancreaticb
fxn.bOtherbcausebonlybmalebsterility.b-bbbANSWERbb

Modifierbgene:bAbgenebthatbaffectsbthebphenotypicbexpressionbofbanotherbgene.bSpecifi
cballelesbofboneborbmorebgenesb(modifierbgenes)bcanbsometimesbdramaticallybmodifybth
ebclinicalbseveritybofbthebphenotypebproducedbbybmutationsbinbabdisease-
causingbgene.Thisbsourcebofbclinicalbheterogeneitybisboftenbreferredbtobasbgeneticbback
ground.bEx.bTwinsbwithbthebsamebmutationbinbcysticbfibrosisbbutbonebisbseverelybsickban
dbonebonlybmoderatelybsick-bexplainedbbybmodifierbgenes.b-bbbANSWERbb

CandidateblocibactingbasbmodifiersbforbCFTRbmutations:TGFB1b(cytokinebtransformingb
growthbfactorbbbandbMLB2b(Mannose-
bindingblectin).bDifferentballelesbofbthesebgenesbmodifybthebseveritybofbCFb-bbbANSWERbb

Clinical/phenotypicbheterogeneity:bmultiplebphenotypesbofbonebsinglebgenebex.bUSH2A
bgene,bcodesbforbproteinbimportantbinbdevelopmentbofbthebinnerbearbandbretina.bCanbbeb

blindbandbdeafb(typebIIbUsherbsyndrome)borbjustbblindb(RetinitisbPigmentosa).b-
bbbANSWERbb




Otherbfactorsbaffectionbphenotypebincludebenvironmentalbfactorsbie.bG6PDbmutationbO
RbsoilbpHbandbhydrangeabcolor.bAlsobSex-
relatedbfactorsbiebHemochromatosis,bAR,bcausedbbybironboverload,bisblessbcommonbinbf
emalesbduebtoblowerbironbintake/menstrualbironbloss.b-bbbANSWERbb

G6PDb(glucose-6-phosphatebdehydrogenase)bDeficiencyb(X-linked)-
bCanbleadbtobhemolyticbanemia,bmanybpplbwithbthisbdisorderbneverbexperiencebanybsym

ptoms.bHemolyticbanemiabcanbbebtriggeredbbybenvironmentalbfactorsbsuchbasbbacterial/
viralbinfections,bdrugb(sulfa,bmalariabmedications),beatingbfavabbeansborbinhalingbfavabb
eanbplantbpollen.b-bbbANSWERbb

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Ricki Lewis, Dr. Human Genetics
Publisher: 2014 ISBN: 9780073525365 Edition: Unknown

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