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遗传搭便车与背景选择对中性变异的联合效应。

Joint effects of genetic hitchhiking and background selection on neutral variation.

作者信息

Kim Y, Stephan W

机构信息

Department of Biology, University of Rochester, Rochester, New York 14627, USA.

出版信息

Genetics. 2000 Jul;155(3):1415-27. doi: 10.1093/genetics/155.3.1415.

Abstract

Due to relatively high rates of strongly selected deleterious mutations, directional selection on favorable alleles (causing hitchhiking effects on linked neutral polymorphisms) is expected to occur while a deleterious mutation-selection balance is present in a population. We analyze this interaction of directional selection and background selection and study their combined effects on neutral variation, using a three-locus model in which each locus is subjected to either deleterious, favorable, or neutral mutations. Average heterozygosity is measured by simulations (1) at the stationary state under the assumption of recurrent hitchhiking events and (2) as a transient level after a single hitchhiking event. The simulation results are compared to theoretical predictions. It is shown that known analytical solutions describing the hitchhiking effect without background selection can be modified such that they accurately predict the joint effects of hitchhiking and background on linked, neutral variation. Generalization of these results to a more appropriate multilocus model (such that background selection can occur at multiple sites) suggests that, in regions of very low recombination rates, stationary levels of nucleotide diversity are primarily determined by hitchhiking, whereas in regions of high recombination, background selection is the dominant force. The implications of these results on the identification and estimation of the relevant parameters of the model are discussed.

摘要

由于强选择的有害突变发生率相对较高,当群体中存在有害突变 - 选择平衡时,预计有利等位基因上会发生定向选择(对连锁中性多态性产生搭便车效应)。我们使用一个三位点模型分析定向选择与背景选择的这种相互作用,并研究它们对中性变异的综合影响,其中每个位点会发生有害、有利或中性突变。平均杂合度通过模拟来测量:(1)在反复发生搭便车事件的假设下处于稳态时;(2)作为单次搭便车事件后的瞬态水平。将模拟结果与理论预测进行比较。结果表明,描述无背景选择时搭便车效应的已知解析解可以修改,从而准确预测搭便车和背景对连锁中性变异的联合效应。将这些结果推广到更合适的多位点模型(使得背景选择可以在多个位点发生)表明,在重组率非常低的区域,核苷酸多样性的稳态水平主要由搭便车决定,而在高重组区域,背景选择是主导力量。讨论了这些结果对模型相关参数识别和估计的影响。

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