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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Substitution processes in molecular evolution. III. Deleterious alleles.
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Substitution processes in molecular evolution. III. Deleterious alleles.

机译:分子进化中的取代过程。三,有害等位基因。

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摘要

The substitution processes for various models of deleterious alleles are examined using computer simulations and mathematical analyses. Most of the work focuses on the house-of-cards model, which is a popular model of deleterious allele evolution. The rate of substitution is shown to be a concave function of the strength of selection as measured by alpha = 2N sigma, where N is the population size and sigma is the standard deviation of fitness. For alpha 1, the house-of-cards model is essentially a neutral model; for alpha 4, the model ceases to evolve. The stagnation for large alpha may be understood by appealing to the theory of records. The house-of-cards model evolves to a state where the vast majority of all mutations are deleterious, but precisely one-half of those mutations that fix are deleterious (the other half are advantageous). Thus, the model is not a model of exclusively deleterious evolution as is frequently claimed. It is argued that there are no biologically reasonable models of molecular evolution where the vast majority of all substitutions are deleterious. Other models examined include the exponential and gamma shift models, the Hartl-Dykhuizen-Dean (HDD) model, and the optimum model. Of all those examined, only the optimum and HDD models appear to be reasonable candidates for silent evolution. None of the models are viewed as good candidates for protein evolution, as none are both biologically reasonable and exhibit the variability in substitutions commonly observed in protein sequence data.
机译:使用计算机模拟和数学分析检查了各种模型的有害等位基因的替代过程。大部分工作都集中在纸牌屋模型上,该模型是有害等位基因进化的流行模型。替代率显示为选择强度的凹函数,通过alpha = 2N sigma来衡量,其中N是种群数量,sigma是适应性的标准偏差。对于alpha <1,纸牌屋模型实质上是中性模型;反之亦然。当alpha> 4时,模型停止发展。大阿尔法的停滞可以通过诉诸记录理论来理解。纸牌屋模型演变成一种状态,其中所有突变中的绝大多数都是有害的,但恰好固定的那些突变中有一半是有害的(另一半是有利的)。因此,该模型不是经常要求的专门有害发展的模型。据认为,没有生物学上合理的分子进化模型,其中所有取代中的绝大多数都是有害的。检查的其他模型包括指数和伽马偏移模型,Hartl-Dykhuizen-Dean(HDD)模型和最佳模型。在所有这些检查中,只有最佳模型和HDD模型似乎是无声进化的合理候选者。没有一个模型被认为是蛋白质进化的良好候选者,因为它们都不具有生物学上的合理性,而且在蛋白质序列数据中通常观察到的替代表现出变异性。

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