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Development f species-specific markers of the tropical oyster (crassostrea belcheri) in thailand

机译:泰国热带牡蛎(crassostrea belcheri)的f种特定标记的发展

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Randomly amplified polymorphic DNA (RAPD) analysis was used to identify species-specific markers of 5 oyster species in Thailand: Crassostrea belcheri,Crassostrea iredalei, Saccostrea cucullata, Saccostrea forskali, and Striostrea (Parastriostrea) mytiloides. Species-specific markers were found in C.belcheri, C.iredalei, and S.cucullata but not in S.forskali and S.mytiloides. Three C.belcheri-specific RAPD fragments were cloned and sequenced. A primer set was designed from each of the recombinant clones (pPACB1, pPACB2, and pPACB3). The polymerase chain reaction products showed expected sizes of 536, 600, and 500bp, respectively, with the sensitivity of detection approximately 30 pg of C.belcheri total DNA template. The specificity of pPACB1 was examined against 135 individuals of indigenous oyster species in Thailand and against outgroup references S.commercialis (N=12) and Perna viridis (N=12). Results indicated the species-specific nature of primers developed from pPACB1. This primer set can be used for broodstock selection and determination of C.belcheri larvae to assist the selective breeding program for this commercially important species.
机译:随机扩增多态性DNA(RAPD)分析用于鉴定泰国5种牡蛎的物种特异性标记:Crassostrea belcheri,Crassostrea iredalei,Saccostrea cucullata,Saccostrea forskali和Striostrea(Parastriostrea)淀粉样蛋白。在C.belcheri,C.iredalei和S.cucullata中发现了物种特异性标记,但在S.forskali和S.mytiloides中没有发现。克隆了三个belcheri特异的RAPD片段并进行了测序。从每个重组克隆(pPACB1,pPACB2和pPACB3)设计引物组。聚合酶链反应产物的预期大小分别为536、600和500bp,检测灵敏度约为30 pg.belcheri总DNA模板。针对泰国的135个本地牡蛎物种和外参考S.commercialis(N = 12)和Perna viridis(N = 12)检查了pPACB1的特异性。结果表明从pPACB1开发的引物具有物种特异性。该引物组可用于亲本选择和测定隐球菌幼虫,以帮助对该商业重要物种进行选择性育种程序。

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