Tokarska M, Marshall T, Kowalczyk R, Wójcik J M, Pertoldi C, Kristensen T N, Loeschcke V, Gregersen V R, Bendixen C
Mammal Research Institute, Polish Academy of Sciences, Białowieza, Poland.
Heredity (Edinb). 2009 Oct;103(4):326-32. doi: 10.1038/hdy.2009.73. Epub 2009 Jul 22.
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.
欧洲野牛(Bison bonasus)在约90年前经历严重瓶颈后已成功恢复,但遗传变异性较低,这可能会严重阻碍亲子关系和个体识别分析。根据系谱分析,当代种群中超过80%的基因仅来自两只奠基动物,近亲繁殖系数平均接近0.5,而微卫星杂合度不超过0.3。我们比较了17个微卫星标记和960个单核苷酸多态性(SNP)标记在欧洲野牛亲子关系和个体识别分析中的有效性。基于微卫星的亲子关系和个体识别分析因标记杂合度低而未成功,在该物种中不是一种实用的方法。使用SNP标记的模拟表明,随机选择80 - 90个位点,或仅50 - 60个杂合度最高的位点,就足以确保在该物种中成功进行亲子关系和个体识别分析。为了规范未来的分析,可以选择一组50 - 60个具有高杂合度且在基因组中分布均匀的牛SNP。可以使用VeraCode(Illumina)或类似的SNP基因分型系统对这组标记进行分型。与16个位点的微卫星检测相比,这些SNP基因分型方法成本较低,这意味着为家养物种开发的现成SNP基因分型系统是相关物种遗传分析的有力工具,即使在其他标记如微卫星的杂合度可能非常低的瓶颈物种中也能有效。