生命科学研究
生命科學研究
생명과학연구
LIFE SCIENCE RESEARCH
2009年
3期
251-257
,共7页
黄建安%李娟%谭月萍%刘硕谦%李勤%刘仲华
黃建安%李娟%譚月萍%劉碩謙%李勤%劉仲華
황건안%리연%담월평%류석겸%리근%류중화
微卫星(microsatellite%SSR)%通用M13引物%毛细管电泳%四色荧光检测%茶树
微衛星(microsatellite%SSR)%通用M13引物%毛細管電泳%四色熒光檢測%茶樹
미위성(microsatellite%SSR)%통용M13인물%모세관전영%사색형광검측%다수
microsatellite%universal M13 primer%capillary electrophoresis%four-color fluorescent
将毛细管电泳四色荧光栓测技术应用于茶树SSR标记分析.该方法采用三引物PCR扩增SSR位点,三引物即在5'端加有M13尾巴序列(5'-CACGACGTTGTAAAACGAC-3')的特异正向引物、特异反向引物及带有荧光标记的通用型M13引物:为了运用四色荧光检测系统使通过一次毛细管电泳能同时检测3个以上的SSR位点,采用蓝、绿、黑3种不同颜色的荧光染料分别对3个M13引物进行标记. 应用该方法对42个茶树品种(系)的16个SSR位点进行遗传分析的结果表明:此法具有简便、可靠、低成本及高通量的优点;且随着所分析SSR位点数的增加,降低成本的效果更加显著.采用建立的方法,还筛选获得了11个多态性丰富的可应用于茶树遗传研究的SSR标记.
將毛細管電泳四色熒光栓測技術應用于茶樹SSR標記分析.該方法採用三引物PCR擴增SSR位點,三引物即在5'耑加有M13尾巴序列(5'-CACGACGTTGTAAAACGAC-3')的特異正嚮引物、特異反嚮引物及帶有熒光標記的通用型M13引物:為瞭運用四色熒光檢測繫統使通過一次毛細管電泳能同時檢測3箇以上的SSR位點,採用藍、綠、黑3種不同顏色的熒光染料分彆對3箇M13引物進行標記. 應用該方法對42箇茶樹品種(繫)的16箇SSR位點進行遺傳分析的結果錶明:此法具有簡便、可靠、低成本及高通量的優點;且隨著所分析SSR位點數的增加,降低成本的效果更加顯著.採用建立的方法,還篩選穫得瞭11箇多態性豐富的可應用于茶樹遺傳研究的SSR標記.
장모세관전영사색형광전측기술응용우다수SSR표기분석.해방법채용삼인물PCR확증SSR위점,삼인물즉재5'단가유M13미파서렬(5'-CACGACGTTGTAAAACGAC-3')적특이정향인물、특이반향인물급대유형광표기적통용형M13인물:위료운용사색형광검측계통사통과일차모세관전영능동시검측3개이상적SSR위점,채용람、록、흑3충불동안색적형광염료분별대3개M13인물진행표기. 응용해방법대42개다수품충(계)적16개SSR위점진행유전분석적결과표명:차법구유간편、가고、저성본급고통량적우점;차수착소분석SSR위점수적증가,강저성본적효과경가현저.채용건립적방법,환사선획득료11개다태성봉부적가응용우다수유전연구적SSR표기.
The capillary electrophoresis with four-color fluorescent detection technique was used to analyze the microsatellites in tea plant. Three primers were used in one PCR reaction for amplification of a defined microsatellite locus by this method. The three primers were as follows: a sequence-specific forward primer tailed with M13-tail at its 5' end, a sequence-specific reverse primer and a universal fluorescent-labeled MI3 primer (5'-CACGACGTTGTAAAACGAC-3'). In order to detect three or more microsatellite loci simultaneously in each capillary electrophoresis through four-color fluorescent detection system, three universal M13 primers were labeled with three different fluorescence dyes (blue,green and black). With this method the genetic analysis of 16 microsatellite loci among 42 tea plants was carried out. The results showed that this method had merits of simple, reliable, cost-effective and high-throughput microsatellite genotyping, and the economy brought by it became greater with an increasing number of microsatellite markers. Also, 11 polymorphie microsatellite markers of tea plant were identified by this method, and these markers would be useful for investigating genetic questions of tea plant (Camellia sinensis ).