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重组进化的通用模型。

A general model for the evolution of recombination.

作者信息

Barton N H

机构信息

Division of Biological Sciences, University of Edinburgh, UK.

出版信息

Genet Res. 1995 Apr;65(2):123-45. doi: 10.1017/s0016672300033140.

DOI:10.1017/s0016672300033140
PMID:7605514
Abstract

A general representation of multilocus selection is extended to allow recombination to depend on genotype. The equations simplify if modifier alleles have small effects on recombination. The evolution of such modifiers only depends on how they alter recombination between the selected loci, and does not involve dominance in modifier effects. The net selection on modifiers can be found explicitly if epistasis is weak relative to recombination. This analysis shows that recombination can be favoured in two ways: because it impedes the response to epistasis which fluctuates in sign, or because it facilitates the response to directional selection. The first mechanism is implausible, because epistasis must change sign over periods of a few generations: faster or slower fluctuations favour reduced recombination. The second mechanism requires weak negative epistasis between favourable alleles, which may either be increasing, or held in check by mutation. The selection (si) on recombination modifiers depends on the reduction in additive variance of log(fitness) due to linkage disequilibria (v1 < O), and on non-additive variance in log(fitness) (V'2, V'3.. for epistasis between 2, 3.. loci). For unlinked loci and pairwise epistasis, si = --(v1 +4V2/3)deltar, where deltar is the average increase in recombination caused by the modifier. The approximations are checked against exact calculations for three loci, and against Charlesworth's analyses of mutation/selection balance (1990), and directional selection (1993). The analysis demonstrates a general relation between selection on recombination and observable components of fitness variation, which is open to experimental test.

摘要

多位点选择的一般表示形式得到扩展,以允许重组依赖于基因型。如果修饰等位基因对重组的影响较小,方程会得到简化。此类修饰基因的进化仅取决于它们如何改变所选位点之间的重组,并且不涉及修饰效应中的显性现象。如果上位性相对于重组较弱,则可以明确找到对修饰基因的净选择。该分析表明,重组可以通过两种方式受到青睐:因为它阻碍了对符号波动的上位性的响应,或者因为它促进了对定向选择的响应。第一种机制不太合理,因为上位性必须在几代人的时间内改变符号:更快或更慢的波动有利于减少重组。第二种机制需要有利等位基因之间存在弱负上位性,这些等位基因可能正在增加,或者受到突变的抑制。对重组修饰基因的选择(si)取决于由于连锁不平衡(v1 < 0)导致的对数适应度加性方差的减少,以及对数适应度的非加性方差(V'2、V'3...用于两位点、三位点...之间的上位性)。对于不连锁的位点和成对上位性,si = –(v1 + 4V2/3)deltar,其中deltar是修饰基因引起的重组平均增加量。针对三个位点的精确计算、以及查尔斯沃思对突变/选择平衡(1990年)和定向选择(1993年)的分析,对这些近似值进行了检验。该分析证明了对重组的选择与适应度变异的可观察成分之间的一般关系,这有待实验检验。

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