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Mutation-selection models of coding sequence evolution with site-heterogeneous amino acid fitness profiles

机译:具有位点异位氨基酸适应性谱的编码序列进化的突变选择模型

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摘要

Modeling the interplay between mutation and selection at the molecular level is key to evolutionary studies. To this end, codon-based evolutionary models have been proposed as pertinent means of studying long-range evolutionary patterns and are widely used. However, these approaches have not yet consolidated results from amino acid level phylogenetic studies showing that selection acting on proteins displays strong site-specific effects, which translate into heterogeneous amino acid propensities across the columns of alignments; related codon-level studies have instead focused on either modeling a single selective context for all codon columns, or a separate selective context for each codon column, with the former strategy deemed too simplistic and the latter deemed overparame-terized. Here, we integrate recent developments in nonparametric statistical approaches to propose a probabilistic model that accounts for the heterogeneity of amino acid fitness profiles across the coding positions of a gene. We apply the model to a dozen real protein-coding gene alignments and find it to produce biologically plausible inferences, for instance, as pertaining to site-specific amino acid constraints, as well as distributions of scaled selection coefficients. In their account of mutational features as well as the heterogeneous regimes of selection at the amino acid level, the modeling approaches studied here can form a backdrop for several extensions, accounting for other selective features, for variable population size, or for subtleties of mutational features, all with parameterizations couched within population-genetic theory.
机译:在分子水平上模拟突变与选择之间的相互作用是进化研究的关键。为此,已经提出了基于密码子的进化模型作为研究远程进化模式的相关手段,并被广泛使用。然而,这些方法尚未综合氨基酸水平系统发育研究的结果,该研究表明,作用于蛋白质的选择表现出较强的位点特异性效应,该效应转化为跨比对列的异构氨基酸倾向。相反,相关的密码子水平研究着重于对所有密码子列建模一个单一的选择上下文,或为每个密码子列建模一个单独的选择上下文,前者的策略被认为过于简单,而后者则被认为是参数设置过高。在这里,我们整合了非参数统计方法的最新发展,以提出一个概率模型,该模型说明了基因编码位置上氨基酸适应度分布图的异质性。我们将该模型应用于十二个真实的蛋白质编码基因比对,并发现其产生生物学上合理的推论,例如,与位点特异性氨基酸限制以及比例选择系数的分布有关。考虑到突变特征以及氨基酸水平上的异质选择机制,本文研究的建模方法可以为一些扩展提供背景,包括其他选择特征,可变种群规模或突变特征的微妙之处。 ,所有这些参数都包含在种群遗传学理论中。

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