Clark A G, Hamilton J F, Chambers G K
Department of Biology, Pennsylvania State University, University Park 16802, USA.
Genetica. 1995;96(1-2):37-49. doi: 10.1007/BF01441150.
A population sample from people of diverse ethnic origins living in New Zealand serves as a database to test methods for inference of population subdivision. The initial null hypothesis, that the population sample is homogeneous across ethnic groups, is easily rejected by likelihood ratio tests. Beyond this, methods for quantifying subdivision can be based on the probability of drawing alleles identical by descent (FST), probabilities of matching multiple locus genotypes, and occurrence of unique alleles. Population genetic theory makes quantitative predictions about the relation between FST, population sizes, and rates of migration and mutation. Some VNTR loci have mutation rates of 10(-2) per generation, but, contrary to theory, we find no consistent association between the degree of population subdivision and mutation rate. Quantification of population substructure also allows us to relate the magnitudes of genetic distances between ethnic groups in New Zealand to the colonization history of the country. The data suggests that the closest relatives to the Maori are Polynesians, and that no severe genetic bottleneck occurred when the Maori colonized New Zealand. One of the central points of contention regarding the application of VNTR loci in forensics is the appropriate means for estimating match probabilities. Simulations were performed to test the merits of the product rule in the face of subpopulation heterogeneity. Population heterogeneity results in large differences in estimates of multilocus genotype frequencies depending on which subpopulation is used for reference allele frequencies, but, of greater importance for forensic purposes, no five locus genotype had an expected frequency greater than 10(-6). Although this implies that a match with an innocent individual is unlikely, in a large urban area such chance matches are going to occur.
来自生活在新西兰的不同种族人群的一个群体样本被用作一个数据库,以测试推断群体细分的方法。最初的零假设,即群体样本在不同种族群体中是同质的,很容易被似然比检验拒绝。除此之外,量化细分的方法可以基于通过家系遗传获得相同等位基因的概率(FST)、匹配多位点基因型的概率以及独特等位基因的出现情况。群体遗传学理论对FST、群体大小以及迁移和突变率之间的关系做出了定量预测。一些VNTR位点每代的突变率为10^(-2),但与理论相反,我们没有发现群体细分程度与突变率之间存在一致的关联。群体亚结构的量化还使我们能够将新西兰不同种族群体之间的遗传距离大小与该国的殖民历史联系起来。数据表明,与毛利人关系最密切的亲属是波利尼西亚人,并且毛利人殖民新西兰时没有发生严重的遗传瓶颈。关于在法医学中应用VNTR位点的一个核心争议点是估计匹配概率的适当方法。进行了模拟以测试乘积法则在面对亚群体异质性时的优点。群体异质性导致根据用于参考等位基因频率的亚群体不同,多位点基因型频率估计值存在很大差异,但对于法医学目的更重要的是,没有一个五位点基因型的预期频率大于10^(-6)。虽然这意味着与无辜个体匹配的可能性不大,但在大城市地区这种偶然匹配还是会发生。