OALib Journal期刊
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gateway技术构建盐和干旱胁迫下水稻根系混合cdna文库及其质量鉴定
DOI: 10.3724/SP.J.1145.2014.00291, PP. 291-294
Keywords: 水稻,抗逆,gateway,cdna文库,盐胁迫,干旱胁迫
Abstract:
为研究水稻非生物胁迫响应信号转导的网络途径,揭示水稻抗逆的分子机制,以nacl胁迫、干旱胁迫处理及正常生长的水稻根系为材料,采用gateway技术构建了水稻根系受盐和干旱诱导的混合cdna文库.cdna文库质量分析表明,未经扩增的原始文库容量为1.5×106cfu,插入片段大小主要为1kb左右,重组率为100%.文库随机挑选克隆测序,结果显示插入序列完整性良好,文库中包含水解酶基因、逆境响应蛋白基因、氧化还原酶基因和富含甘氨酸的rna结合蛋白质基因等.因此,本研究构建的盐和干旱诱导的水稻根系混合cdna文库符合高质量文库的标准,可以用于进一步开展相关基因的克隆及功能研究.
References
[1] | 5sargenttd,dawidib.differentialgeneexpressioninthegastrulaofxenopuslaevis[j].science,1983,222:135-139
|
[2] | 7diatchenkol,lauyf,campbellap,chenchika,moqadamf,huangb,siebertpd.suppressionsubtractivehybridization:amethodforgeneratingdifferentiallyregulatedortissue-specificcdnaprobesandlibraries[j].procnatacadsci,1996,93:6025-6030.
|
[3] | 8ederyi,chull,sonenbergn,pelletierj.anefficientstrategytoisolatefull-lengthcdnasbasedonanmrnacapretentionprocedure(capture)[j].molcellbiol,1995,15:3363-3371
|
[4] | 9katzenf.gatewayrecombinationalcloning:abiologicaloperatingsystem[j].expertopindrugdiscov,2007,2:571-589
|
[5] | 10cheodl,titussa,byrddr,hartleyjl,templegf,brasch,ma.concertedassemblyandcloningofmultiplednasegmentsusinginvitrosite-specificrecombination:functionalanalysisofmulti-segmentexpressionclones[j].genomeres,2004,14:2111-2120
|
[6] | 11jiangy,deyholosm.comprehensivetranscriptionalprofilingofnacl-stressedarabidopsisrootsrevealsnovelclassesofresponsivegenes[j].bmcplantbiol,2006,6:25
|
[7] | 13janghj,pihkt,kangsg,limjh,jinjb,piaohl,wangh.molecularcloningofanovelca2+-bindingproteinthatisinducedbynaclstress[j].plantmolbiol,1998,37:839-847
|
[8] | 14zikm,arazit,sneddenwa,frommh.twoisoformsofglutamatedecarboxylaseinarabidopsisareregulatedbycalcium/calmodulinanddifferinorgandistribution[j].plantmolbiol,1998,37:967-975
|
[9] | 15kudlaj,xuq,harterk,gruissemw,luans.genesforcalcineurinb-likeproteinsinarabidopsisaredifferentiallyregulatedbystresssignals[j].procnatacadsci,1999,96:4718-4723
|
[10] | 16opassirir,pomthongb,onkoksoongt,akiyamat,esena,cairnsjr.analysisofriceglycosylhydrolasefamily1andexpressionofos4bglu12β-glucosidase[j].bmcplantbiol,2006,6:33
|
[11] | 17xuz,escamilla-trevi?ol,zengl,lalgondarm,bevand,winkelb,esena.functionalgenomicanalysisofarabidopsisthalianaglycosidehydrolasefamily1[j].plantmolbiol,2004,55:343-367
|
[12] | 18kwakkj,kimyo,kangh.characterizationoftransgenicarabidopsisplantsoverexpressinggr-rbp4underhighsalinity,dehydration,orcoldstress[j].jexpbot,2005,56:3007-3016
|
[13] | 19kimjy,parksj,jangb,jungch,ahnsj,gohch,kangh.functionalcharacterizationofaglycine-richrna-bindingprotein2inarabidopsisthalianaunderabioticstressconditions[j].plantj,2007,50:439-451
|
[14] | 20chenx,zengqc,luxp,yudq,liwz.characterizationandexpressionanalysisoffourglycine-richrna-bindingproteinsinvolvedinosmoticresponseintobacco[j].agricscichina,2010,9:1577-1587
|
[15] | 21ascenzir,ganttjs.adrought-stress-induciblehistonegeneinarabidopsisthalianaisamemberofadistinctclassofplantlinkerhistonevariants[j].plantmolbiol,1997,34:629-641
|
[16] | 1yamaguchit,blumwalde.developingsalt-tolerantcropplants:challengesandopportunities[j].trendsplantsci,2005,10:615-620
|
[17] | 2vinocurb,altmana.recentadvancesinengineeringplanttolerancetoabioticstress:achievementsandlimitations[j].curropinbiotechnol,2005,16:123-132
|
[18] | 3bohnerthj,nelsonde,jensenrg.adaptationstoenvironmentalstresses[j].plantcell,1995,7:1099-1111
|
[19] | 4ashwanik,takabet.abioticstresstoleranceinplants[m].springer,2010
|
[20] | 6schramlp,shipmanr,stulzp,ludwigcu.cdnasubtractionlibraryconstructionusingamagnet-assistedsubtractiontechnique(mast)[j].trendsgenet,1993,9:70-76
|
[21] | 12uraot,yakubovb,satohr,yamaguchi-shinozakik,sekim,hirayamat,shinozakik.atransmembranehybrid-typehistidinekinaseinarabidopsisfunctionsasanosmosensor[j].plantcell,1999,11:1743-1754
|
[22] | 22wesslersr.plantretrotransposons:turnedonbystress[j].currbiol,1996,6:959-961
|
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