武汉植物学研究
武漢植物學研究
무한식물학연구
JOURNAL OF WUHAN BOTANICAL RESEARCH
2007年
5期
427-431
,共5页
EST%微卫星%SSR%多态性%烟草
EST%微衛星%SSR%多態性%煙草
EST%미위성%SSR%다태성%연초
EST%Microsatellites%SSR%Polymorphism%Tobacco
利用MISA软件对烟草EST公共数据库中的简单重复序列(SSRs)进行了分析.结果表明,在133 523条EST序列中,共获得81 757条SSR序列,SSRs之间的距离约为0.92 kb.其中,六碱基重复丰度最大,占60.3%,而单碱基、三碱基、四碱基、二碱基和五碱基重复丰度分别为20.0%、11.0%、4.2%、2.8%和1.7%.在单碱基、二碱基、三碱基和四碱基重复模体中,丰度最大的分别是A/T、AG、AAG和AAAT,而CG在编码区内丰度很低.用CAP3软件进行冗余分析表明,在这6种类型的重复模体中,冗余与非冗余的烟草EST之间没有显著差异.在得到的SSR序列中随机选择10个序列设计引物,在7个烟草品种中进行PCR扩增.结果表明,10对引物全部扩增出PCR产物,其中8对引物扩增出预期片段.用这8组扩增出预期片段的PCR产物进行变性PAGE凝胶电泳检测,结果表明,其中有4对引物(EB4、EB5、EB6和EB8)扩增出多态性条带.
利用MISA軟件對煙草EST公共數據庫中的簡單重複序列(SSRs)進行瞭分析.結果錶明,在133 523條EST序列中,共穫得81 757條SSR序列,SSRs之間的距離約為0.92 kb.其中,六堿基重複豐度最大,佔60.3%,而單堿基、三堿基、四堿基、二堿基和五堿基重複豐度分彆為20.0%、11.0%、4.2%、2.8%和1.7%.在單堿基、二堿基、三堿基和四堿基重複模體中,豐度最大的分彆是A/T、AG、AAG和AAAT,而CG在編碼區內豐度很低.用CAP3軟件進行冗餘分析錶明,在這6種類型的重複模體中,冗餘與非冗餘的煙草EST之間沒有顯著差異.在得到的SSR序列中隨機選擇10箇序列設計引物,在7箇煙草品種中進行PCR擴增.結果錶明,10對引物全部擴增齣PCR產物,其中8對引物擴增齣預期片段.用這8組擴增齣預期片段的PCR產物進行變性PAGE凝膠電泳檢測,結果錶明,其中有4對引物(EB4、EB5、EB6和EB8)擴增齣多態性條帶.
이용MISA연건대연초EST공공수거고중적간단중복서렬(SSRs)진행료분석.결과표명,재133 523조EST서렬중,공획득81 757조SSR서렬,SSRs지간적거리약위0.92 kb.기중,륙감기중복봉도최대,점60.3%,이단감기、삼감기、사감기、이감기화오감기중복봉도분별위20.0%、11.0%、4.2%、2.8%화1.7%.재단감기、이감기、삼감기화사감기중복모체중,봉도최대적분별시A/T、AG、AAG화AAAT,이CG재편마구내봉도흔저.용CAP3연건진행용여분석표명,재저6충류형적중복모체중,용여여비용여적연초EST지간몰유현저차이.재득도적SSR서렬중수궤선택10개서렬설계인물,재7개연초품충중진행PCR확증.결과표명,10대인물전부확증출PCR산물,기중8대인물확증출예기편단.용저8조확증출예기편단적PCR산물진행변성PAGE응효전영검측,결과표명,기중유4대인물(EB4、EB5、EB6화EB8)확증출다태성조대.
Simple sequence repeats (SSRs) of tobacco expressed sequence tags (EST) in public database were investigated by using computer program MISA (MIcroSAtellite).Up to 81 757 SSRs were found in 133 523 sequences and the average distance between SSRs was approximately 0.92 kb.Among them,hexanucleotide repeats (60.3%) were the most abundance,while the monomeric,trimeric,tetrameric,dimeric,and pentameric repeats are represented in decreasing proportions of 20.0%,11.0%,4.2%,2.8%,and 1.7%,respectively.The most abundant motif was A/T,AG,AAG and AAAT in monomeric,dimeric,trimeric,and tetrameric repeats,respectively.Whereas CG rich repeats are rarely found in the coding regions.The redundancy analysis indicated that no significant differences were observed between the redundant and non-redundant set of tobacco ESTs in individual SSR motifs.Ten pairs of primers flanking EST-SSR loci were designed to detect the polymorphism in seven tobacco cultivars.The analyses on denatured PAGE by silver staining confirmed the existence of polymorphism by these four pairs of primers of EB4,EB5,EB6,and EB8 among the seven tobacco cultivars.The SSR loci reported in this study are the first molecular DNA-based genetic markers developed from public ESTs database in tobacco.The EST-SSR markers will be useful information resource for germplasm characterization and crop improvement through genetic mapping and marker-assisted selection in tobacco.