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首页> 外文期刊>Zoological Science >Sex Determination and Individual Identification of American Minks (Neovison vison) on Hokkaido, Northern Japan, by Fecal DNA Analysis
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Sex Determination and Individual Identification of American Minks (Neovison vison) on Hokkaido, Northern Japan, by Fecal DNA Analysis

机译:通过粪便DNA分析确定日本北海道美国水貂(Neovison vison)的性别并进行个体鉴定

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摘要

To determine the sex and identity of individual American minks (Neovison vsion), a species introduced into Japan, molecular genetic methods were employed on fecal samples collected from the Kushiro Wetland, eastern Hokkaido. We examined the sex chromosome-linked genes ZFX and ZFY and 11 microsatellite loci to identify individuals. From microsatellite genotypes, the probability of identity was calculated to distinguish between individuals with 99% certainty. To evaluate the accuracy of the genotyping results, we used two approaches for several randomly selected samples. In the first approach, we genotyped all samples from the results of a maximum of three independent polymerase chain reactions (PCRs). In the second approach, we genotyped 10% of the samples from the results of five independent PCRs. Samples subsequent genotypings disagreed with the first genotype were counted as one of three categories of error. The results indicated that genotyping more than 10 microsatellite loci was required to reduce the probability of error in identity to less than 0.01. Twenty of 72 fecal samples were genotyped at 10 or 11 microsatellite loci and sex-determined by ZFX/ZFY genes, resulting in identification of five males and nine females. In assessing the accuracy of the results, genotyping errors were found to have occurred in 20% of the first genotypes. The main type of error was 'missing data', which can be prevented by increasing the number of replicate PCRs.
机译:为了确定引入美国的单个水貂(Neovison vsion)的性别和身份,对从北海道东部the路湿地采集的粪便样本采用了分子遗传学方法。我们检查了性染色体连锁基因ZFX和ZFY和11个微卫星基因座,以鉴定个体。从微卫星基因型中,计算出同一性的可能性,以区分具有99%确定性的个体。为了评估基因分型结果的准确性,我们对几种随机选择的样本使用了两种方法。在第一种方法中,我们根据最多三个独立的聚合酶链反应(PCR)的结果对所有样品进行基因分型。在第二种方法中,我们根据五个独立PCR的结果对10%的样品进行了基因分型。不符合第一个基因型的样本随后的基因分型被视为错误的三类之一。结果表明,需要对超过10个微卫星基因座进行基因分型,才能将身份错误的概率降低至小于0.01。在10个或11个微卫星基因座上对20个粪便样本中的20个进行了基因分型,并由ZFX / ZFY基因确定性别,从而鉴定出5名男性和9名女性。在评估结果的准确性时,发现有20%的第一个基因型发生了基因分型错误。错误的主要类型是“丢失数据”,这可以通过增加重复PCR的数量来避免。

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