Chakraborty R, Daiger S P
Center for Demographic and Population Genetics, Graduate School of Biomedical Science Center, Houston 77225.
Hum Biol. 1991 Oct;63(5):571-87.
Apparent departure from equilibrium of genetic parameters measured for multiallelic single-locus markers such as VNTR (variable number of tandem repeat) loci has been suggested as evidence of underlying heterogeneity of the tested population. Using allele frequency distributions at eight VNTR loci from the white population of Utah, we show that the observed number of alleles and the gene diversity at each locus are congruent according to expectations of the neutral mutation model. This demonstrates the genetic homogeneity of the white population of Utah with reference to the allele (total and rare) frequency distribution at eight VNTR loci. The importance of such procedures is discussed in the context of using VNTR polymorphism data for forensic and medicolegal applications. Recommendations for reporting population data for hypervariable loci are also made to aid potential users in conducting similar analyses.
对于多等位基因单基因座标记(如可变串联重复序列(VNTR)基因座)所测量的遗传参数明显偏离平衡,这被认为是受试群体存在潜在异质性的证据。利用来自犹他州白人种群的8个VNTR基因座的等位基因频率分布,我们发现,根据中性突变模型的预期,每个基因座观察到的等位基因数量和基因多样性是一致的。这证明了犹他州白人种群在8个VNTR基因座的等位基因(总数和稀有基因)频率分布方面的遗传同质性。在将VNTR多态性数据用于法医和法医学应用的背景下,讨论了此类程序的重要性。还提出了关于报告高变基因座群体数据的建议,以帮助潜在用户进行类似分析。