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1、中国水稻科学(ChinJRiceSci),2014,28(5):465-472http://www.ricesci.cnDOI:10.3969/ji.ssn.1001G7216.2014.05.003465水稻类病变突变体g303的鉴定和基因定位刘林1,#张迎信1,#李枝1,2刘群恩1余宁1孙滨1杨正福1周全1程式华1曹立勇1,∗(1中国水稻研究所/国家水稻改良中心/浙江省超级稻研究重点实验室,杭州310006;2杭州师范大学生命与环境科学学院,杭州310036;#共同第一作者;∗通讯联系人,EGma
2、il:caolycgf@mail.hz.zj.cn)CharacterizationandGeneMappingofaLesionMimicMutantg303inRiceLIULin1,#,ZHANGYingGxin1,#,LIZhi1,2,LIUQunGen1,YUNing1,SUNBin1,YANGZhengGfu1,ZHOUQuan1,CHENGShiGhua1,CAOLiGyong1,∗(1ZhejiangKeyLaboratoryofSuperRice/NationalCenterforR
3、iceImprovement/ChinaNationalRiceResearchInstitute,Hangzhou310006,China;2CollegeofLifeandEnvironmentalSciences,HangzhouNormalUniversity,Hangzhou310036,China;#Theseauthorscontributedequallytothispaper;∗Correspondingauthor,EGmail:caolycgf@mail.hz.zjc.n)LIU
4、Lin,ZHANGYingxin,LIZhi,etal.Characterizationandgenemappingofalesionmimicmutantg303inrice.ChinJRiceSci,2014,28(5):465G472.Abstract:Thelesionmimicmutantg303andg342wereisolatedbytreatingtheseedsofindicavarieties9311andR8015withγGrayradiation,respectively.T
5、heyellowspotsinitiallyappearong303leavesat4Gleafstage.Withthegrowthanddevelopmentoftheplant,thelesionsalmostoccupiedthewholeplanttillthematuritystage.Comparedwiththewildtype,theplantheight,seedsettingrateand1000Ggrainweightofg303significantlydropped,the
6、chlorophyllandphotosyntheticrateobviouslydecreased.Geneticanalysisshowedthatthemutantphenotypewascontrolledbyasinglerecessivegene.UsingF2mappingpopulationofg303/Nipponbare,theg303mutantgenewasmappedbetweenmarkerInD10andInD12onricechromosome12,withgeneti
7、cdistancesof0.19cMand0.76cM,respectively.SequenceanalysisrevealedthatthemutatedgenewasallelictoSL,g303andg342mutatedgenehadasinglenucleotidedeletion(T572andG1206,respectively),leadingtoaprematureterminationcodon.RealGtimePCRanalysisshowedthattheexpressi
8、onlevelofdefenseGrelatedgenesupregulatedsignificantly,theseresultsdemonstratedthatthemutationmayactivatethedefenseresponse.Keywords:rice;lesionmimicmutant;genemapping;defenseresponse刘林,张迎信,李枝,等.水稻类病变突变体g303的鉴定和基因定位.中国水稻科学,2014,28