Cutler D J
Center for Population Biology, University of California, Davis, California 95616, USA.
Genetics. 2000 Mar;154(3):1403-17. doi: 10.1093/genetics/154.3.1403.
Rates of molecular evolution at some protein-encoding loci are more irregular than expected under a simple neutral model of molecular evolution. This pattern of excessive irregularity in protein substitutions is often called the "overdispersed molecular clock" and is characterized by an index of dispersion, R(T) > 1. Assuming infinite sites, no recombination model of the gene R(T) is given for a general stationary model of molecular evolution. R(T) is shown to be affected by only three things: fluctuations that occur on a very slow time scale, advantageous or deleterious mutations, and interactions between mutations. In the absence of interactions, advantageous mutations are shown to lower R(T); deleterious mutations are shown to raise it. Previously described models for the overdispersed molecular clock are analyzed in terms of this work as are a few very simple new models. A model of deleterious mutations is shown to be sufficient to explain the observed values of R(T). Our current best estimates of R(T) suggest that either most mutations are deleterious or some key population parameter changes on a very slow time scale. No other interpretations seem plausible. Finally, a comment is made on how R(T) might be used to distinguish selective sweeps from background selection.
在分子进化的简单中性模型下,一些蛋白质编码位点的分子进化速率比预期的更不规则。蛋白质替换中这种过度不规则的模式通常被称为“过度分散的分子钟”,其特征是分散指数R(T)>1。在分子进化的一般平稳模型下,假设无限位点,给出了基因R(T)的无重组模型。结果表明,R(T)仅受三件事影响:发生在非常缓慢时间尺度上的波动、有利或有害突变以及突变之间的相互作用。在没有相互作用的情况下,有利突变会降低R(T);有害突变会提高R(T)。根据这项工作分析了先前描述的过度分散分子钟模型以及一些非常简单的新模型。结果表明,有害突变模型足以解释观察到的R(T)值。我们目前对R(T)的最佳估计表明,要么大多数突变是有害的,要么某些关键种群参数在非常缓慢的时间尺度上发生变化。似乎没有其他合理的解释。最后,对如何使用R(T)来区分选择性清除和背景选择进行了评论。