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微卫星三重PCR基因扫描技术在中国明对虾家系标识中的应用

Parentage identification of Chinese shrimp(Fenneropenaeus chinensis) using microsatellite-based triplex PCR Genescan technology

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【作者】 孔杰高焕于飞罗坤王伟继孟宪红刘萍张天时

【Author】 KONG Jie~(1),GAO Huan~(2),YU Fei~(3),LUO Kun~(3),MENG Xian-hong~(1),LIU Ping~(1),ZHANG Tian-shi~(1)(1.Key Laboratory for Sustainable Utilization of Marine Fisheries Resources,Ministry of Agriculture,Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences,Qingdao 266071,China;2.Jiangsu Key Laboratory of Marine Biotechnology,Huaihai Institute of Technology,Lianyungang 222005,China;3.Shanghai Fisheries University,Shanghai 200090,China)

【机构】 农业部海洋渔业资源可持续利用重点开放实验室中国水产科学研究院黄海水产研究所淮海工学院江苏省海洋生物技术重点建设实验室上海水产大学农业部海洋渔业资源可持续利用重点开放实验室中国水产科学研究院黄海水产研究所 山东青岛266071江苏连云港222005上海200090山东青岛266071

【摘要】 在开发中国明对虾(Fenneropenaeus chinensis)微卫星引物的基础上,利用3对微卫星引物,克隆编号分别为H081、RS0683和RS1101,构建中国明对虾的三重PCR稳定扩增体系。在此基础上,进一步利用荧光标记引物的基因扫描技术(Genescan)对利用精荚移植技术建立的中国明对虾7个半同胞家系和16个全同胞家系进行识别研究。结果表明,该项技术可以准确地把7个半同胞家系的子代个体间、16个全同胞家系的子代个体间以及总的31个全同胞家系的子代个体间区别开,且能准确把这些家系产生的任意子代个体定位到各个家系。该技术可以满足大批量家系材料样本的分析,具有较好的应用价值。[中国水产科学,2007,14(1):59-66]

【Abstract】 In 2005,we developed many full-and half-sibs of Chinese shrimp(Fenneropenaeus chinensis).In order to perform the genetic breeding program of Chinese shrimp,the offspring from deferent parentages were needed to cultivate together.Here,the problem is how to distinguish the offspring belonging to each parentage from each other.We attempted to use microsatellite molecular markers to resolve it.Through developing the microsatellite primers from the random genome sequences of F.chinensis,we obtained some microsatellite markers with rich genetic polymorphic information,in which three markers,RS1101,RS0683 and H081 were selected to establish a triplex PCR technique using a touch-down PCR method.The expected bands of three markers were clearly presented in the 8% denature polyacrylamide gel by electrophoresing,and the optimal amplified PCR reaction volume was 15 μL containing 10×Buffer(1.3 μL,)MgCl2(2.5 mmol/L)1.0 μL,dNTP1.0 μL(2.5 mmol/L),0.5 μL of each forward or reverse primer(20 pmol/μL),1.5 μL template DNA(50ng/μL),7 μL ddH2O and 0.2 μL Taq Polymerase(1 U).Furthermore,the amplification products of trilex PCR were analyzed using ABI 3 700 Prism Genetic Analyzer and GeneScan 4.0 software(Perkin Elmer Applied Biosystems),and Gene Maper3.0 software.In seven half-sibs and sixteen full-sibs,6,24 and 24 alleles were found on the RS1101,RS0683 and H081 loci,respectively.By the comparative analysis on genotypes between parents and offspring,the results showed that the offspring of seven half-sibs and sixteen full-sibs could be identified from each other.Additionally,by the help of Cervus bio-soft(Version 2.0,written by Triston),any offspring cultivated together could be found which parentage they belong to.So,the triplex PCR is a useful tool for the parentage identification of Chinese shrimps.[Journal of Fishery Sciences of China,2007,14(1):59-66]

【基金】 国家自然科学基金项目(30500378);国家高技术研究发展计划863项目(2005AA60310)
  • 【文献出处】 中国水产科学 ,Journal of Fishery Sciences of China , 编辑部邮箱 ,2007年01期
  • 【分类号】S917.4
  • 【被引频次】36
  • 【下载频次】363
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