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在穆勒棘轮作用下克隆谱系的固定

Fixation of clonal lineages under Muller's ratchet.

作者信息

Gabriel W, Bürger R

机构信息

Zoologisches Institut der Ludwig-Maximilians-Universität München, Germany.

出版信息

Evolution. 2000 Aug;54(4):1116-25. doi: 10.1111/j.0014-3820.2000.tb00547.x.

Abstract

For clonal lineages of finite size that differ in their deleterious mutational effects, the probability of fixation is investigated by mathematical theory and Monte Carlo simulations. If these fitness effects are sufficiently small in one or both lineages, then the lineage with the less deleterious effects will become fixed with high probability. If, however, in both lineages the deleterious effects are larger than a threshold s(c), then the probability of fixation is independent of the fitness effects and depends only on the initial frequencies of the lineages. This threshold decreases with decreasing genomic mutation rate U and increases with population size N. (For N = 10(5), we have s(c) approximately = 0.1 if U = 1, and s(c) approximately = 0.015 if U = 0.1). Above the threshold, the competition is not driven by the ratio of mean fitnesses of the lineages, but by the relative sizes of the zero-mutation classes, which are independent of the fitness effects of the mutations. After the loss of the zero-mutation class of a lineage, the other lineage will spread to fixation with high probability and within a short time span. If the mutation rates of the lineages differ substantially, the lineage with the lower mutation rate is fixed with very high probability unless the lineage with the larger mutation rate has very slightly deleterious mutational effects. If the mutation rates differ by not more than a few percent, then the lineage with the higher mutation rate and the more deleterious effects can become fixed with appreciable probability for a certain range of parameters. The independence of the fixation probability on the fitness effects in a single population leads to dramatic effects in metapopulations: lineages with more deleterious effects have a much higher fixation probability. The critical value s(c), above which this phenomenon occurs, decreases as the migration rate between the subpopulations decreases.

摘要

对于具有不同有害突变效应的有限大小的克隆谱系,通过数学理论和蒙特卡罗模拟研究固定概率。如果这些适合度效应在一个或两个谱系中足够小,那么具有较小有害效应的谱系将以高概率固定。然而,如果在两个谱系中有害效应都大于阈值s(c),那么固定概率与适合度效应无关,仅取决于谱系的初始频率。该阈值随着基因组突变率U的降低而降低,随着种群大小N的增加而增加。(对于N = 10⁵,如果U = 1,我们有s(c)约为0.1;如果U = 0.1,s(c)约为0.015)。高于阈值时,竞争不是由谱系平均适合度的比率驱动,而是由零突变类别的相对大小驱动,这与突变的适合度效应无关。在一个谱系的零突变类别消失后,另一个谱系将以高概率在短时间内扩散至固定。如果谱系的突变率有很大差异,除非具有较大突变率的谱系具有非常轻微的有害突变效应,否则具有较低突变率的谱系将以非常高的概率固定。如果突变率相差不超过百分之几,那么对于一定范围的参数,具有较高突变率和更有害效应的谱系可以以可观的概率固定。单个种群中固定概率与适合度效应的独立性在集合种群中会产生显著影响:具有更有害效应的谱系具有高得多的固定概率。出现这种现象的临界值s(c)随着亚种群之间迁移率的降低而降低。

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