Clark A G
Department of Biology, Pennsylvania State University, University Park 16802.
Am J Hum Genet. 1987 Nov;41(5):948-56.
The allele frequency data of Baird et al. were tested using Ewens-Watterson sampling theory for goodness of fit to the infinite-alleles model of neutral evolution. Although probes of both the HRAS-1 and D14S1 loci identify highly diverse restriction-fragment-length polymorphisms, the observed values of gene identity (F) and the common allele frequency (C) are not significantly different from the neutral expectation. Allele frequency distributions show a tendency toward a deficit in diversity for HRAS-1 and a slight excess diversity for D14S1. The direction of these departures is consistent with potential selective effects of the Harvey-ras oncogene and hitchhiking of the D14S1 locus to closely linked immunoglobulin genes. Direct chi 2-tests of goodness of fit of the observed and expected allele frequency distributions reveal significant departures in the caucasoid and Hispanic HRAS-1 distributions but not in any of the other tests.
使用尤因斯 - 沃特森抽样理论对贝尔德等人的等位基因频率数据进行检验,以确定其与中性进化的无限等位基因模型的拟合优度。尽管HRAS - 1和D14S1位点的探针都识别出高度多样的限制性片段长度多态性,但观察到的基因同一性(F)值和常见等位基因频率(C)与中性预期值并无显著差异。等位基因频率分布显示,HRAS - 1存在多样性不足的趋势,而D14S1则有轻微的多样性过剩。这些偏离的方向与哈维 - 拉斯癌基因的潜在选择效应以及D14S1位点与紧密连锁的免疫球蛋白基因的搭便车现象一致。对观察到的和预期的等位基因频率分布进行直接卡方拟合优度检验发现,在白种人和西班牙裔人群的HRAS - 1分布中存在显著偏离,但在其他任何检验中均未发现。