首页> 外文期刊>Heredity: An International Journal of Genetics >Effectiveness of microsatellite and SNP markers for parentage and identity analysis in species with low genetic diversity: the case of European bison.
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Effectiveness of microsatellite and SNP markers for parentage and identity analysis in species with low genetic diversity: the case of European bison.

机译:微卫星和SNP标记在遗传多样性低的物种中进行亲缘关系和同一性分析的效力:欧洲野牛案例。

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摘要

The European bison (Bison bonasus) has recovered successfully after a severe bottleneck about 90 years ago but has been left with low genetic variability that may substantially hinder parentage and identity analysis. According to pedigree analysis, over 80% of the genes in the contemporary population descend from just two founder animals and inbreeding coefficients averaged almost 0.5, whereas microsatellite heterozygosity does not exceed 0.3. We present a comparison of the effectiveness of 17 microsatellite and 960 single nucleotide polymorphism (SNP) markers for paternity and identity analysis in the European bison. Microsatellite-based paternity and identity analysis was unsuccessful because of low marker heterozygosity and is not a practical approach in this species. Simulations using SNP markers suggest that 80-90 randomly selected loci, or just 50-60 of the most heterozygous loci, would be sufficient to ensure successful paternity and identity analysis in this species. For the purpose of standardizing future analysis, a panel of 50-60 bovine SNPs characterized by high heterozygosity and an even distribution in the genome could be selected. This panel of markers could be typed using VeraCode (Illumina) or similar SNP genotyping systems. The low cost of these SNP genotyping methods compared with a 16 locus microsatellite survey means that off-the-shelf SNP genotyping systems developed for domestic species represent powerful tools for genetic analysis in related species, and can be effective even in bottlenecked species in which heterozygosity of other markers such as microsatellites may be very low.
机译:欧洲野牛(Bison bonasus)在大约90年前经历了严重的瓶颈后已成功恢复,但是遗传变异性较低,可能会严重阻碍亲子鉴定和身份分析。根据谱系分析,当代人口中超过80%的基因仅来自两只创始人动物,近交系数平均接近0.5,而微卫星杂合度不超过0.3。我们目前比较欧洲野牛的亲子鉴定和身份分析中的17个微卫星和960个单核苷酸多态性(SNP)标记的有效性。基于微卫星的亲子鉴定和身份分析由于标记物杂合度低而未能成功,因此在该物种中不可行。使用SNP标记进行的模拟表明,随机选择80-90个基因座,或者最杂合的基因座中只有50-60个,足以确保对该物种成功进行亲子鉴定和身份分析。为了标准化将来的分析,可以选择一组具有高杂合度和基因组均匀分布的50-60个牛SNP。可以使用VeraCode(Illumina)或类似的SNP基因分型系统对标记物进行分型。与16位微卫星调查相比,这些SNP基因分型方法的成本低,这意味着为国内物种开发的现成SNP基因分型系统代表了相关物种遗传分析的强大工具,即使在杂合性为瓶颈的物种中也可以有效其他标记(例如微卫星)的数量可能非常低。

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