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自然群体中黑腹果蝇基因变异的综合研究。II.杂合度估计和地理分化模式。

A Comprehensive Study of Genic Variation in Natural Populations of Drosophila melanogaster. II. Estimates of Heterozygosity and Patterns of Geographic Differentiation.

机构信息

Department of Biology, McMaster University, Hamilton, Ontario, L8S 4K1, Canada.

出版信息

Genetics. 1987 Oct;117(2):255-71. doi: 10.1093/genetics/117.2.255.

Abstract

A study of genic variation in natural population of D. melanogaster was undertaken (1) to obtain a better estimate of heterozygosity by sampling a relatively large number of gene loci and (2) to identify different groups of polymorphic loci whose variation patterns might suggest different kinds of selection forces. A total of 117 gene loci (coding for 79 enzymes and 38 abundant proteins) were studied in 15 geographically distant populations originating from different continents. The findings of this study are as follows: (1) of the 117 gene loci studied, 61 are polymorphic and 56 are uniformly monomorphic everywhere. (2) An average population is polymorphic for 43% of its gene loci and an average individual is heterozygous for 10% of its gene loci. These estimates are remarkably similar among populations. (3) The average within-locality heterozygosity (H(S)) for polymorphic loci is uniformly distributed over the range of heterozygosity observed; i.e. , given that a locus has any local variation, it is nearly as likely to have a lot as a little. (4) The distribution of F(ST) (fixation index) is strongly skewed, with a prominent mode at 8-10% and a long tail of high values reaching a maximum of 58%. Two-thirds of all loci fall within the bell-shaped distribution centered on an F(ST) of 8-10%, a result compatible with the notion that they are experiencing a common tendency toward small interlocality differences owing to extensive gene flow among populations. (5) The distribution of total heterozygosity (H(T)) has a prominent bimodal distribution. The lower mode consists of loci with single prominent allele and a few uncommon ones and the upper mode consists of clinally varying loci with a high F(ST ) (e.g., Adh and G6-pd), loci with many alleles in high frequency (e.g., Ao and Xdh) and loci with two alleles in high frequency in all populations but, with little interpopulational differentiation (e.g., Est-6 and alpha-Fuc). The loci in the lower mode are probably under purifying selection; a large proportion of those in the latter mode may be under balancing selection. (6) Comparison of genic variation for loci located inside vs. outside inversions, comparison of F(ST) for inversions and their associated genes, and comparison of F(ST) and map position for pairs of loci all suggest that, while linkage has some influence, it does not seem to constrain the pattern of variation that a locus may develop. (7) Eighteen polymorphic loci show latitudinal variation in allele frequencies which are consistent in populations from different continents. (8) Estimates of Nei genetic distance between population pairs are generally low between populations on the same continent and high between populations on different continents. There are two important exceptions: population pairs for which both localities are in the temperate zone show no relationship to distance, and in cases where both populations are tropical or subtropical, the genetic distance is higher than for the temperate-tropical comparisons and seem even higher than one would expect from the geographic distance separating them. The latter observation suggests that either geographic separation outweighs differences in environment in determining the genetic composition of a population or that all tropical populations are not experiencing the same environment.-The results are discussed in relation to the neutralist-selectionist controversy of genic variation and two important conclusions are drawn: First, there is a negative correlation between the number of loci sampled and the resulting heterozygosity. This means that available estimates of heterozygosity, 85% of which are based on 30 or fewer loci, are high and hence not appropriate for making between-taxa comparisons. Secondly, there is a group of loci, comprising one-third of polymorphic loci (or about 15% of all loci studied), that is distinguishable by different patterns of variation within and among populations. Most of these loci have clinal variation which is consistent with the hypothesis that their genetic variation is maintained by balancing selection.

摘要

对自然种群中的基因变异进行了研究(1)通过对大量基因座进行抽样,以更好地估计杂合度,(2)鉴定不同群体的多态基因座,这些基因座的变异模式可能暗示着不同的选择压力。在来自不同大陆的 15 个地理上遥远的种群中,共研究了 117 个基因座(编码 79 种酶和 38 种丰富蛋白)。这项研究的结果如下:(1)在所研究的 117 个基因座中,61 个是多态的,61 个是无处不在的均匀单态的。(2)一个平均种群的基因座有 43%是多态的,个体的基因座有 10%是杂合的。这些估计在种群之间非常相似。(3)多态基因座的本地异质性(H(S))的平均值均匀分布在观察到的异质性范围内;即,如果一个基因座具有任何本地变异,它几乎与具有大量变异的基因座一样可能具有少量变异。(4)F(ST)(固定指数)的分布强烈偏斜,模式突出在 8-10%之间,高值的长尾延伸至最大值 58%。三分之二的基因座落在以 8-10%的 F(ST)为中心的钟形分布内,这一结果与由于种群之间广泛的基因流导致种群间局部差异趋于小的概念一致。(5)总异质性(H(T))的分布具有明显的双峰分布。较低的模式由具有单个突出等位基因和少数罕见等位基因的基因座组成,较高的模式由具有高 F(ST)(例如,Adh 和 G6-pd)的渐变基因座组成,具有高频率的许多等位基因(例如,Ao 和 Xdh)和具有高频率的两个等位基因的基因座,但在所有种群中,与种群间的分化很小(例如,Est-6 和 alpha-Fuc)。较低模式中的基因座可能受到净化选择的影响;后者模式中的大部分基因座可能受到平衡选择的影响。(6)比较位于反转内部和反转外部的基因座的基因变异,比较反转及其相关基因的 F(ST),以及比较一对基因座的 F(ST)和图谱位置,所有这些都表明,虽然连锁有一定的影响,但它似乎并没有限制一个基因座可能发展的变异模式。(7)18 个多态基因座在不同大陆的种群中表现出等位基因频率的纬度变化,这些变化在种群中是一致的。(8)种群对之间的 Nei 遗传距离估计通常在同一大陆的种群之间较低,而在不同大陆的种群之间较高。有两个重要的例外:当地点都在温带的种群对之间没有关系,而在热带或亚热带的种群之间,遗传距离高于温带-热带比较,甚至高于从它们之间的地理距离预期的水平。后一种观察表明,要么地理分离在确定种群的遗传组成方面超过了环境差异,要么所有热带种群都没有经历相同的环境。-结果与基因变异的中性主义-选择主义争议有关,并得出两个重要结论:第一,样本基因座的数量与所得杂合度之间存在负相关。这意味着,可用的杂合度估计值中有 85%是基于 30 个或更少的基因座得出的,这些估计值偏高,因此不适合进行种间比较。其次,有一组基因座,占多态基因座的三分之一(或研究的所有基因座的 15%),通过种群内和种群间的不同变异模式可以区分开来。这些基因座中的大多数具有渐变的变异模式,这与它们的遗传变异是由平衡选择维持的假设一致。

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