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Epigenomic Consequences of Immortalized Plant Cell Suspension Culture 英文参考文献
o
PL SBIOLOGY
EpigenomicConsequencesofImmortalized
PlantCellSuspensionCulture
Milos Tanurdzic1,Matthew W. Vaughn1,Hongmei Jiang2,Tae-Jin Lee3,R.Keith Slotkin1,Bryon Sosinski3,
William F.Thompson4,R.W. Doerge5,Robert A.Martienssen1
1ColdSpringHarborLaboratory,ColdSpringHarbor,NewYork,UnitedStatesofAmerica,2DepartmentofStatistics,NorthwesternUniversity,Evanston,Illinois,United
StatesofAmerica,3DepartmentofHorticulturalScience,NorthCarolinaStateUniversity,Raleigh,NorthCarolina,UnitedStatesofAmerica,4DepartmentsofPlantBiology,
Genetics,andCropScience,NorthCarolinaStateUniversity,Raleigh,NorthCarolina,UnitedStatesofAmerica,5DepartmentsofStatisticsandAgronomy,PurdueUniversity,
WestLafayette,Indiana,UnitedStatesofAmerica
Plant cells grown in culture exhibit genetic and epigenetic instability. Using a combination of chromatin
immunoprecipitation and DNA methylation profiling on tiling microarrays, we have mapped the location and
abundanceofhistoneandDNAmodificationsinacontinuouslyproliferating,dedifferentiatedcellsuspensionculture
ofArabidopsis.Wehavefoundthateuchromatinbecomeshypermethylatedincultureandthatasmallpercentageof
the hypermethylated genes become associated with heterochromatic marks. In contrast, the heterochromatin
undergoes dramatic and very precise DNA hypomethylation with transcriptional activation of specific transposable
elements(TEs)inculture.HighthroughputsequencingofsmallinterferingRNA(siRNA)revealedthatTEsactivatedin
culture have increased levels of 21-nucleotide (nt) siRNA, sometimes at the expense of the 24-nt siRNA class. In
contrast,TEsthatremainsilent,whichmatchthepredominant24-ntsiRNAclass,donotchangesignificantlyintheir
siRNAprofiles.TheseresultsimplicateRNAinterferenceandchromatinmodificationinepigeneticrestructuringofthe
genomefollowingtheactivationofTEsinimmortalizedcellculture.
Citation:TanurdzicM,VaughnMW,JiangH,LeeTJ,SlotkinRK,etal.(2008)Epigenomicconsequencesofimmortalizedplantcellsuspensionculture.PLoSBiol6(12):e302.
doi:10.137
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