首页> 外文期刊>Aquaculture >Development of two new microsatellite multiplex PCRs for three sparid species: Gilthead seabream (Sparus auratus L.), red porgy (Pagrus pagrus L.) and redbanded seabream (P. auriga, Valenciennes, 1843) and their application to paternity studies
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Development of two new microsatellite multiplex PCRs for three sparid species: Gilthead seabream (Sparus auratus L.), red porgy (Pagrus pagrus L.) and redbanded seabream (P. auriga, Valenciennes, 1843) and their application to paternity studies

机译:为三种spa属物种开发了两个新的微卫星多重PCR:Gilthead鲷(Sparus auratus L.),红斑豚(Pagrus pagrus L.)和Redbanded鲷(P. auriga,Valenciennes,1843)及其在亲子关系研究中的应用

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This study reports two new and highly informative multiplex PCRs of microsatellite markers, with redesigned interspecific primer sets for three sparid species: gilthead seabream (Sparus auratus L.), red porgy (Pagrus pagrus L.) and redbanded seabream (P. auriga, Valenciennes, 1843). The evaluation and validation of the two multiplex PCRs, named RimA and RimB (Redesigned Interspecific Multiplex), were carried out upon: 148 individual gilthead seabream (66 breeders of unknown gender, and 82 of their descendents obtained by mass-spawning), 37 red porgy and 125 redbanded seabream. From 15 and 12 redesigned microsatellite markers for RimA and RimB, respectively, the number of markers included in the final multiplex PCRs were 10 in RimA and 7 in RimB for gilthead seabream, 6 in each multiplex PCR for red porgy and 8 in RimA and 5 in RimB for redbanded seabream. The a priori combined parental exclusion probability for each multiplex in the three species was 0.999. For gilthead seabream, it was possible to assign each offspring to a single parent pair (100% success) using the exclusion method with at least seven microsatellite markers for each multiplex PCR. Null alleles were found only for marker PbMS2, through familial segregation, with a frequency similar to the expected one (0.09 vs 0.14). Results revealed that the multiplex reaction no more than one-sixth the cost of single reactions even when these reactions were performed in a unique run, and that genotyping errors were minimized due to automation. These robust multiplex PCRs will be a fundamental tool for the industry to introduce selection programs and to manage their broodstocks under industrial conditions.
机译:这项研究报告了两种新的,具有高度信息量的微卫星标记多重PCR,并为三种spa科物种重新设计了种间引物集:t头鲷(Sparus auratus L.),红海豚(Pagrus pagrus L.)和红斑鲷(P. auriga,Valenciennes) (1843年)。对以下两个多重PCR的评估和验证:RimA和RimB(重新设计的种间多重):148个体金头鲷(66种不明性别的繁殖者,其82个后代通过大量产卵获得繁殖),37个红色海豚和125条红鲷。经过重新设计的15个和12个重新设计的RimA和RimB微卫星标记,最终多重PCR中包含的标记数量分别为:RimA中为10个,对于金头鲷,RimB中为7个,对于红斑豚鱼,每个多重PCR中为6个,RimA和5个中为8个在RimB中获得红带鲷。三个物种中每个多重性的先验组合父母排斥概率为0.999。对于金头鲷,可以使用排除方法将每个后代分配给一对亲本(100%成功),每个多重PCR至少要有七个微卫星标记。通过家族分离仅发现标记PbMS2的无效等位基因,其频率与预期的频率相似(0.09比0.14)。结果表明,即使以独特的方式进行多重反应,多重反应的成本也不会超过单个反应成本的六分之一,并且由于自动化,基因分型错误得以最小化。这些强大的多重PCR将成为行业引入选择程序并在工业条件下管理亲虾的基本工具。

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