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1、中国水稻科学(ChinJRiceSci),2015,29(4):357-362http://www.ricesci.cnDOI:10.3969/ji.ssn.1001G7216.2015.04.004357水稻矮秆多分蘖突变体bf370的遗传分析和基因定位胡运高1,2杨国涛2郭连安2钦鹏1陈永军2李仕贵1,∗(1四川农业大学水稻研究所,成都611130;2西南科技大学水稻研究所,四川绵阳621010;∗通讯联系人,EGmail:lishiguiGsc@263.net)GeneticAnalysisandMappingofaDwarfandHighGtilleringMutantbf370
2、inRiceHUYunGgao1,2,YANGGuoGtao2,GUOLianGan2,QINPeng1,CHENYongGjun2,LIShiGgui1,∗(1RiceResearchInstitute,SichuanAgriculturalUniversity,Chengdu611130,China;2RiceResearchInstitute,SouthwestUniversityofScienceandTechnology,Mianyang621010,China;∗Correspondingauthor,EGmail:lishiguiGsc@263.net)HUYungao,Y
3、ANGGuotao,GUOLianan,etal.GeneticanalysisandmappingofadwarfandhighGtilleringmutantbf370inrice.ChinJRiceSci,2015,29(4):357G362.Abstract:AdwarfandhighGtilleringmutantbf370wasobtainedfromtheindicaricevarietyHong’aiBbyneutronradiation.Comparedwiththewildtype,themutantbf370wascharacterizedbydwarfplanta
4、ndmoretillers.Thenumberoftillersinbf370wasabout200,whichwas13timesmorethanthatinthewildtype.Geneticanalysisindicatedthatthisphenotypewascontrolledbyasinglerecessivenucleargene,whichwasmappedtoa398kbregionbetweenthemarkerIndel4andIndel10onthelongarmofchromosome1usingtheF2mappingpopulationgenerated
5、fromthecrossbetweenmutantbf370andNipponbare.Sequencinganalysisshoweda66nucleotidedeletioninthesecondexonofD10,resultingina22aminoacidsdeletioninthepredictedRPE65domainofD10proteininthebf370mutant.Combinedwiththephenotypeofotherd10mutants,thephenotypeofbf370waslikelycausedbya66nucleotidedeletionin
6、D10.Keywords:rice;dwarfmutant;highGtillering;geneticanalysis;mapping胡运高,杨国涛,郭连安,等.水稻矮秆多分蘖突变体bf370的遗传分析和基因定位.中国水稻科学,2015,29(4):357G362.摘要:通过中子辐射诱变早籼稻品种红矮B,获得矮秆多分蘖突变体bf370.该突变体与野生型相比表现为植株矮化,分蘖极多.bf370在全生育期内的分蘖数达200个左右,是野生型分蘖数量的14倍以上.遗传分析表明该矮秆多分蘖突变体表型受一对隐性核基因控制.利用突变体bf370与日本晴杂交构建的F2群体将突变基因定位到第1染色体长臂
7、Indel4与Indel10之间398kb区域内.测序分析发现,与野生型相比突变体该区段内的D10基因在第2外显子上缺失66bp碱基,导致D10蛋白RPE65结构域22个氨基酸缺失.结合D10其他突变体表型推断,bf370表型极有可能由D10突变所致.关键词:水稻;矮秆突变体;多分蘖;遗传分析;基因定位中图分类号:Q343?5;S511?032文献标识码:A文章编号:1001G7216(2015)04G0357G06水稻是人类的主要