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中国梨s?rnase基因启动子的tail?pcr克隆及功能预测

DOI: 10.3969/j.jssn.1000-2006.2010.04.005, PP. 21-25

Keywords: tail?pcr,,s?rnase,启动子

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Abstract:

利用tail?pcr技术从中国砂梨品种‘金花’、‘懋功’及白梨品种‘鸭梨’基因组dna中分别扩增出长度为854、1448和1137bp的s13-、s12-、s21-rnase基因5′端上游序列,并提交genbank,序列号为hm047239、hm047240、hm047241。经place和plantcare软件顺式调控元件预测发现,这3个启动子均具有典型核心启动子tata盒和caat盒,且在上游均存在光应答调控元件(box4,g?box)、脱落酸应答元件abre及水杨酸应答元件tca?element等,由此可知其可能受光照、脱落酸、水杨酸等多种条件的共同调节。此外,与已知日本梨s2-、s3-、s4-、s5-rnase基因启动子序列比对发现,s?rnase启动子tata盒上游存在一约200bp的同源区域。以meg4.0构建系统发育树表明,梨属和苹果属s?rnase等位基因多态性可能在亚科的分化之前就已形成。

References

[1]  mattondp,mausl,okamotos,etal.thes?locusofnicotianaalata:genomicorganizationandsequenceanalysisoftwos?rnasealleles[j].plantmolbiol,1995,28:847-858.
[2]  morgandr,soltisde,robertsonkr.systematicandevolutionaryimplicationsofrbclsequencevariationinrosaceae[j].amjbot,1994,81:890-903.
[3]  prellh.dasproblemderunfruchtbarkeit[j].naturewochschr,nf,1921,20:440-446.(责任编辑郑琰?)第34卷第4期2010年7月南京林业大学学报(自然科学版)journalofnanjingforestryuniversity(naturalscienceedition)vol.34,no.4jul.,2010
[4]  王绪,邓俭英,方锋学,等.issr分子标记技术及其在园艺作物中的应用[j].广西农业科学,2007,38(4):371-374.
[5]  satoy,kuriharaa,ogatat,etal.modeofself?compatibilityinheritanceinjapanesepear[j].jjpnsochortsci,1988,supp(2):76-77.
[6]  liuyg,whittierrf.thermalasymmetricinterlacedpcr:automatableamplificationandsequencingofinsertendfragmentsfromp1andyacclonesforchromosomewalking[j].genomics,1995,25:674-681.
[7]  liuyg,mitsukawan,oosumit,etal.efficientisolationandmappingofarabidopsisthalianat?dnainsertjunctionsbythermalasymmetricinterlacedpcr[j].plant,1995,8:457-463.
[8]  higok,ugaway,iwamotom,etal.plantcis?actingregulatorydnaelements(place)database[j].nuclacidsres,1999,27:297-300.
[9]  lescotm,déhaisp,thijsg,etal.plantcare,adatabaseofplantcis?actingregulatoryelementsandaportaltotoolsforinsilicoanalysisofpromotersequences[j].nuclacidsres,2002,30:325-327.
[10]  dissanayakedmrkk,noriokas,noriokan,etal.cis?regulatoryelementsforpistilspecificexpressionins?rnasepromoterregionofjapanesepear(pyruspyrifolianakai)[j].actahort,2002,587:459-465.
[11]  kaufmannh,salaminif,thompsonrd.sequencevariabilityandgenestructureattheself?incompatibilitylocusofsolanumtuberosum[j].molgengenet,1991,226:457-466.
[12]  colemance,kaot?h.the5′flankingregionsoftwopetuniainflatasallelesareheterogeneousandrepetitivesequences[j].plantmolbiol,1992,18:499-511.
[13]  chungik,leesy,itot,etal.the5′flankingsequencesoftwosallelesinlycopersiconperuvianumarehighlyheterologousbutcontainshortblocksofhomologoussequences[j].plantcellphysiol,1995,36:1621-1627.
[14]  tsugekir,kochievaez,fedoroffnv.atransposoninsertioninthearabidopsisssr16genecausesanembryo?defectivelethalmutation[j].theplantjournal,1996,10(3):479-489.
[15]  乌云塔娜.中国白梨自交不亲和基因的分离鉴定[d].长沙:中南林业科技大学,2003.
[16]  thompsonjd,gibsontj,plewniakf,etal.theclustalxwindowsinterface:flexiblestrategiesformultiplesequencealignmentaidedbyqualityanalysistools[j].nucleicacidsresearch,1997,25:4876-4882.
[17]  tamurak,dudleyj,neim,etal.mega4:molecularevolutionarygeneticsanalysis(mega)softwareversion4.0[j].molecularbiologyandevolution,2007:1596-1599.
[18]  ushijimak,sassah,hiranoh.characterizationoftheflankingregionsofthes?rnasegenesofjapanesepear(pyrusserotina)andapple(malus×domestica)[j].gene,1998,211:159-167.
[19]  noriokan,katayamah,matsukit,etal.sequencecomparisonofthe5′flankingregionsofjapanesepear(pyruspyrifolianaki)s?rnasesassociatedwithgametophyticself?incompatibility[j].sexplant,2001,13:289-291.

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