Transcriptome analysis of stem development in the tumourous stem mustard Brassica juncea var. tumida Tsen et Lee by RNA sequencing 英文参考文献.docVIP
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Transcriptome analysis of stem development in the tumourous stem mustard Brassica juncea var. tumida Tsen et Lee by RNA sequencing 英文参考文献
Sunetal.BMCPlantBiology2012,12:53
/1471-2229/12/53
RESEARCH ARTICLE
OpenAccess
Transcriptomeanalysisofstemdevelopmentin
thetumourousstemmustardBrassicajunceavar.
tumidaTsenetLeebyRNAsequencing
QuanSun1,GuanfanZhou2,YingfanCai1*,YonghongFan2,XiaoyanZhu1,3,YihuaLiu2,XiaohongHe1,
JinjuanShen2,HuaizhongJiang1,DaiwenHu2,ZhengPan1,LiuxinXiang1,GuanghuaHe3,DaiwenDong2and
JianpingYang1
Abstract
Background:Tumourousstemmustard(Brassicajunceavar.tumidaTsenetLee)isaneconomicallyand
nutritionallyimportantvegetablecropoftheCruciferaefamilythatalsoprovidestherawmaterialforFuling
mustard.Thegeneticsbreeding,physiology,biochemistryandclassificationofmustardshavebeenextensively
studied,butlittleinformationisavailableontumourousstemmustardatthemolecularlevel.Togaingreater
insightintothemolecularmechanismsunderlyingstemswellinginthisvegetableandtoprovideadditional
informationformolecularresearchandbreeding,wesequencedthetranscriptomeoftumourousstemmustardat
variousstemdevelopmentalstagesandcompareditwiththatofamutantvarietylackingswollenstems.
Results:UsingIlluminashort-readtechnologywithatag-baseddigitalgeneexpression(DGE)system,we
performeddenovotranscriptomeassemblyandgeneexpressionanalysis.Inouranalysis,weassembledgenetic
informationfortumourousstemmustardatvariousstemdevelopmentalstages.Inaddition,weconstructedfive
DGElibraries,whichcoveredthestrainsYong’anandDayejieatvariousdevelopmentstages.Illuminasequencing
identified146,265unigenes,including11,245clustersand135,020singletons.Theunigenesweresubjectedtoa
BLASTsearchandannotatedusingtheGOandKOdatabases.Wealsocomparedthegeneexpressionprofilesof
threeswollenstemsampleswiththoseoftwonon-swollenstemsamples.Atotalof1,042geneswithsignificantly
differentexpressionlevelsoccurringsimultaneouslyinthesixcomparisongroupswerescreenedout.Finally,the
alteredexpressionlevelsofanumberofrandomlyselectedgeneswereconfirmedbyquantitativereal-timePCR.
Conclusions:Ourdataprovidecomprehensivegeneexpressioninformationatthetranscriptionallevelandthe
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