Center for Demographic and Population Genetics, University of Texas at Houston, Texas 77025.
Genetics. 1980 Apr;94(4):1039-63. doi: 10.1093/genetics/94.4.1039.
With the aim of understanding the mechanism of maintenance of protein polymorphism, we have studied the properties of allele frequency distribution and the number of alleles per locus, using gene-frequency data from a wide range of organisms (mammals, birds, reptiles, amphibians, Drosophila and non-Drosophila invertebrates) in which 20 or more loci with at least 100 genes were sampled. The observed distribution of allele frequencies was U-shaped in all of the 138 populations (mostly species or subspecies) examined and generally agreed with the theoretical distribution expected under the mutation-drift hypothesis, though there was a significant excess of rare alleles (gene frequency, 0 approximately 0.05) in about a quarter of the populations. The agreement between the mutation-drift theory and observed data was quite satisfactory for the numbers of polymorphic (gene frequency, 0.05 approximately 0.95) and monomorphic (0.95 approximately 1.0) alleles.-The observed pattern of allele-frequency distribution was incompatible with the prediction from the overdominance hypothesis. The observed correlations of the numbers of rare alleles, polymorphic alleles and monomorphic alleles with heterozygosity were of the order of magnitude that was expected under the mutation-drift hypothesis. Our results did not support the view that intracistronic recombination is an important source of genetic variation. The total number of alleles per locus was positively correlated with molecular weight in most of the species examined, and the magnitude of the correlation was consistent with the theoretical prediction from mutation-drift hypothesis. The correlation between molecular weight and the number of alleles was generally higher than the correlation between molecular weight and heterozygosity, as expected.
为了理解蛋白质多态性维持的机制,我们使用来自广泛的生物体(哺乳动物、鸟类、爬行动物、两栖动物、果蝇和非果蝇无脊椎动物)的基因频率数据,研究了等位基因频率分布和每个基因座的等位基因数的特性,其中 20 个或更多个基因座具有至少 100 个基因。在 138 个(大多数是物种或亚种)被检查的群体中,观察到的等位基因频率分布呈 U 形,并且总体上与突变-漂移假设下预期的理论分布一致,尽管在大约四分之一的群体中存在大量稀有等位基因(基因频率,0 约为 0.05)。在数量上,突变-漂移理论与观察数据之间的一致性相当令人满意,包括多态性(基因频率,0.05 约为 0.95)和单态性(0.95 约为 1.0)等位基因。观察到的等位基因频率分布模式与超显性假说的预测不一致。观察到的稀有等位基因、多态性等位基因和单态性等位基因的数量与杂合度的相关性在突变-漂移假说下是预期的数量级。我们的结果不支持内含子重组是遗传变异的重要来源的观点。在大多数检查的物种中,每个基因座的等位基因总数与分子量呈正相关,并且相关的大小与突变-漂移假说的理论预测一致。与杂合度相比,分子量与等位基因数量之间的相关性通常更高,这是预期的。