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岳根华, Balazs Kovacs, Laszlo Orban, . 2010: 微卫星跨物种交叉PCR扩增的一个新问题:扩增非同源产物(英文). 动物学研究, 31(2): 131-140. DOI: 10.3724/SP.J.1141.2010.02131
引用本文: 岳根华, Balazs Kovacs, Laszlo Orban, . 2010: 微卫星跨物种交叉PCR扩增的一个新问题:扩增非同源产物(英文). 动物学研究, 31(2): 131-140. DOI: 10.3724/SP.J.1141.2010.02131
YUE Gen-Hua , *, Balazs Kovacs, Laszlo Orban, *. 2010. A New Problem with Cross-Species Amplification of Microsatellites: Generation of Non-Homologous Products. Zoological Research, 31(2): 131-140. DOI: 10.3724/SP.J.1141.2010.02131
Citation: YUE Gen-Hua , *, Balazs Kovacs, Laszlo Orban, *. 2010. A New Problem with Cross-Species Amplification of Microsatellites: Generation of Non-Homologous Products. Zoological Research, 31(2): 131-140. DOI: 10.3724/SP.J.1141.2010.02131

微卫星跨物种交叉PCR扩增的一个新问题:扩增非同源产物(英文)

A New Problem with Cross-Species Amplification of Microsatellites: Generation of Non-Homologous Products

  • 摘要: 微卫星已被广泛应用于群体遗传学、生态学和进化生物学研究。然而,一些物种微卫星尚未克隆。为了节省时间和经费,研究人员往往使用一个物种已发表的微卫星引物扩增其近缘物种的微卫星。该研究对属于3个不同科(Clariidae、Heteropneustidae 和Pimelodidae)的7个鲶鱼物种的微卫星跨物种PCR扩增产物进行了序列分析,研究发现扩增非同源(non-orthologous)产物是微卫星跨物种PCR扩增的一个新问题。该研究共采用4对胡子鲶微卫星座位引物对7个鲶鱼物种进行了跨物种PCR扩增。对获得的204个PCR产物的序列分析结果表明,两对微卫星座位引物扩增了所有7个物种的同源特异产物。而其他两个座位的引物扩增了特异但非同源的多态产物,对近缘物种的扩增也获得类似结果。另外,除胡子鲶等位基因大小异源同型(size homoplasy)的特征不明显外,其他物种在3个微卫星座位都具有这一非常明显的特征。这些数据表明,微卫星跨物种间交叉扩增能产生非同源产物;等位基因大小异源同型与微卫星座位本身有关,而与物种间的亲缘关系无明显的相关性。微卫星跨物种扩增产生的非同源产物和等位基因大小异源同型将使系统发育、群体遗传学和进化研究明显复杂化。因此,在应用微卫星跨物种交叉扩增数据以前,最好对跨物种交叉扩增产物进行测序验证。

     

    Abstract: Microsatellites have been widely used in studies on population genetics, ecology and evolutionary biology. However, microsatellites are not always available for the species to be studied and their isolation could be time-consuming. In order to save time and effort researchers often rely on cross-species amplification. We revealed a new problem of microsatellite cross-species amplification in addition to size homoplasy by analyzing the sequences of electromorphs from seven catfish species belonging to three different families (Clariidae, Heteropneustidae and Pimelodidae). A total of 50 different electromorphs were amplified from the seven catfish species by using primers for 4 microsatellite loci isolated from the species Clarias batrachus. Two hundred and forty PCR-products representing all 50 electromorphs were sequenced and analyzed. Primers for two loci amplified specific products from orthologous loci in all species tested, whereas primers for the other two loci produced specific and polymorphic bands from some non-orthologous loci, even in closely related non-source species. Size homoplasy within the source species was not obvious, whereas extensive size homoplasy across species were detected at three loci, but not at the fourth one. These data suggest that amplification of products from non-orthologous loci and appearance of size homoplasy by cross-amplification are locus dependent, and do not reflect phylogenetic relationship. Amplification of non-orthologous loci and appearance of size homoplasy will lead to obvious complications in phylogenetic interference, population genetic and evolutionary studies. Therefore, we propose that sequence analysis of cross-amplification products should be conducted prior to application of cross-species amplification of microsatellites.

     

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