全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
药学学报  2015 

基于cdna-srap技术筛选的atp合成酶cf1-α亚单位基因(ctl-spn)与红花刺性状紧密连锁

, PP. 1052-1059

Keywords: 红花,有刺/无刺,cdna-srap,atp合成酶

Full-Text   Cite this paper   Add to My Lib

Abstract:

红花的花是传统的活血化瘀中药,但因其花序周围苞叶有刺非常不利于人工采摘。本研究采用cdna-srap技术分析了与红花苞叶刺性状紧密连锁的基因。在分别建立红花f2代cdna无刺池和有刺池的基础上,利用60对引物筛选与苞叶刺连锁的基因片段,获得6条与红花刺性状连锁的基因片段,其中基因gpy-1和gpy-2重组率低,与苞叶刺紧密连锁并成功测序。采用race技术,克隆了gpy-2cdna全长,命名为ctl-spn,生物信息学分析显示:ctl-spn全长1679bp,具有1524bp的开放阅读框,编码508个氨基酸。同源比对发现:ctl-spn表达蛋白与其他物种的atp合成酶cf1-α亚基具有很高的同源性(97%)。半定量rt-pcr分析结果显示:gpy-1和gpy-2仅在有刺f2代单株中表达。因此,红花atp合成酶cf1-α亚基基因(ctl-spn)可能直接参与了红花刺性状的形成从而提高了有刺红花的抗逆性,这一发现为红花无刺品种的选育提供了重要思路。

References

[1]  mouekoubald,zhangll,guanx,etal.analysisofclonostachysrosea-inducedresistancetotomatograymolddiseaseintomatoleaves[j].plosone,2014,9:e102690.
[2]  garavagliabs,thomasl,zimarot,etal.aplantnatriureticpeptide-likemoleculeofthepathogenxanthomonasaxonopodispv.citricausesrapidchangesintheproteomeofitscitrushost[j].bmcplantbiol,2010,10:51.
[3]  wulj,wangsx,chenx,etal.proteomicandphytohormoneanalysisoftheresponseofmaize(zeamaysl.)seedlingstosugarcanemosaicvirus[j].plosone,2013,8:e70295.
[4]  romanowskae,powikrowskam,zienkiewiczm,etal.highlightinducedaccumulationoftwoisoformsofthecf1alpha-subunitinmesophyllandbundlesheathchloroplastsofc4plants[j].actabiochimpol,2008,55:175-182.
[5]  burkeyko,mathisjn.identificationofanovelisoformofthechloroplast-couplingfactoralpha-subunit[j].plantphysiol,1998,116:703-708.
[6]  shaohh,caoq,taox,etal.cloningandcharacterizationofatpsynthasecf1αgenefromsweetpotato[j].afrjbiotechnol,2011,10:19035-19042.
[7]  bowlesvg,mayerhoferr,davisc,etal.aphylogeneticinvestigationofcarthamuscombiningsequenceandmicrosatellitedata[j].plantsystevol,2010,287:85-97.
[8]  pahlavanimh,mirlohiaf,saeidig.inheritanceofflowercolorandspininessinsafflower(carthamustinctoriusl.)[j].jhered,2004,95:265-267.
[9]  johnstonam,tanakadl,millerpr,etal.oilseedcropsforsemiaridcroppingsystemsinthenortherngreatplains[j].agronj,2002,94:231-240.
[10]  crossrl,mullerv.theevolutionofa-,f-,andv-typeatpsynthasesandatpases:reversalsinfunctionandchangesintheh+/atpcouplingratio[j].febslett,2004,576:1-4.
[11]  siowyl,choypc,leungwm,etal.effectoffloscarthamionstress-activatedproteinkinaseactivityintheisolatedreperfusedratheart[j].molcellbiochem,2000,207:41-47.
[12]  guoqh,guoml.srapfragmentslinkedtospinesofcarthamustinctorius[j].actapharmsin(药学学报),2007,42:94-797.
[13]  huangcq,liugd,baicj,etal.applicationofsrapmarkersintheidentificationofstylosanthesguianensishybrids[j].molbiolrep,2014,41:5923-5929.
[14]  lig,quiroscf.sequence-relatedamplifiedpolymorphism(srap),anewmarkersystembasedonasimplepcrreaction:itsapplicationtomappingandgenetagginginbrassica[j].theorapplgenet,2001,103:455-461.
[15]  ferriolm,picób,nuezf.geneticdiversityofagermplasmcollectionofcucurbitapepousingsrapandaflpmarkers[j].theorapplgenet,2003,107:271-282.
[16]  linzx,zhangxl,nieyc.evaluationofapplicationofanewmolecularmarkersraponanalysisoff2segregationpopulationandgeneticdiversityincotton[j].jgenetgenomics,2004,31:622-626.
[17]  lig,gaom,yangb,etal.geneforgenealignmentbetweenthebrassicaandarabidopsisgenomesbydirecttranscriptomemapping[j].theorapplgenetics,2003,107:168-180.
[18]  michelmorerw,parani,kesselirv.identificationofmarkerslinkedtodisease-resistancegenesbybulkedsegregantanalysis:arapidmethodtodetectmarkersinspecificgenomicregionsbyusingsegregatingpopulations[j].procnatlacadsciusa,1991,88:9828-9832.
[19]  dongreab,rautmp,bhandarkarmr,etal.identificationandgeneticpuritytestingofcottonf1hybridusingmolecularmarkers[j].indianjbiotechnol,2011,10:301-306.
[20]  vernonsd,ungerer,rajeevanm,etal.reproducibilityofalternativeprobesynthesisapproachesforgeneexpressionprofilingwitharrays[j].jmoldiagn,2000,2:124-127.
[21]  fengn,liyk,tangj,etal.cdna-aflpanalysisontranscriptsassociatedwithhydroxysaffloryellowa(hsya)biosyntheticpathwayincarthamustinctorius[j].biochemsystecol,2010,38:971-980.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133