Transpositional reactivation of the Dart transposon family in rice lines derived from introgressive hybridization with Zizania latifolia 英文参考文献.docVIP
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Transpositional reactivation of the Dart transposon family in rice lines derived from introgressive hybridization with Zizania latifolia 英文参考文献
Wangetal.BMCPlantBiology2010,10:190
/1471-2229/10/190
RESEARCH ARTICLE
OpenAccess
TranspositionalreactivationoftheDart
transposonfamilyinricelinesderivedfrom
introgressivehybridizationwithZizanialatifolia
NingningWang1,HongyanWang1,2,HuiWang1,DiZhang1,YingWu1,XiufangOu1,ShuangLiu1,ZhenyingDong1,
BaoLiu1*
Abstract
Background:Itiswidelyrecognizedthatinterspecifichybridizationmayinduce“genomeshock”,andleadto
geneticandepigeneticinstabilitiesintheresultanthybridsand/orbackcrossedintrogressants.Aprominent
componentinvolvedinthegenomeshockisreactivationofcryptictransposableelements(TEs)inthehybrid
genome,whichisoftenassociatedwithalterationintheelements’epigeneticmodificationslikecytosineDNA
methylation.WehavepreviouslyreportedthatintrogressantsderivedfromhybridizationbetweenOryzasativa(rice)
andZizanialatifoliamanifestedsubstantialmethylationre-patterningandrampantmobilizationoftwoTEs,acopia
retrotransposonTos17andaMITEmPing.ItwasnotknownhoweverwhetherothertypesofTEshadalsobeen
transpositionallyreactivatedintheseintrogressants,theirrelevancetoalterationincytosinemethylation,andtheir
impactonexpressionofadjacentcellulargenes.
Results:WedocumentinthisstudythattheDartTEfamilywastranspositionallyreactivatedfollowedby
stabilizationinallthreestudiedintrogressants(RZ1,RZ2andRZ35)derivedfromintrogressivehybridization
betweenrice(cv.Matsumae)andZ.latifolia,whiletheTEsremainedquiescentintherecipientricegenome.
Transposon-display(TD)andsequencingverifiedtheelement’smobilityandmappedtheexcisionsandre-
insertionstothericechromosomes.Methylation-sensitiveSouthernblottingshowedthattheDartTEswereheavily
methylatedalongtheirentirelength,andmoderatealterationincytosinemethylationpatternsoccurredinthe
introgressantsrelativetotheirriceparentalline.Real-timeqRT-PCRquantificationontherelativetranscript
abundanceofsixsingle-copygenesflankingthenewlyexcisedorinsertedDart-relatedTEcopiesindicatedthat
whereasmarkeddifferenceintheexpressionofallfourgenesinbothtissues(leafandroot)weredetected
be
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