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Markovian and non-Markovian protein sequence evolution: aggregated Markov process models.

机译:马尔可夫和非马尔可夫蛋白序列的进化:聚集的马尔可夫过程模型。

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摘要

Over the years, there have been claims that evolution proceeds according to systematically different processes over different timescales and that protein evolution behaves in a non-Markovian manner. On the other hand, Markov models are fundamental to many applications in evolutionary studies. Apparent non-Markovian or time-dependent behavior has been attributed to influence of the genetic code at short timescales and dominance of physicochemical properties of the amino acids at long timescales. However, any long time period is simply the accumulation of many short time periods, and it remains unclear why evolution should appear to act systematically differently across the range of timescales studied. We show that the observed time-dependent behavior can be explained qualitatively by modeling protein sequence evolution as an aggregated Markov process (AMP): a time-homogeneous Markovian substitution model observed only at the level of the amino acids encoded by the protein-coding DNA sequence. The study of AMPs sheds new light on the relationship between amino acid-level and codon-level models of sequence evolution, and our results suggest that protein evolution should be modeled at the codon level rather than using amino acid substitution models.
机译:多年来,有人声称进化是在不同的时间尺度上根据系统上不同的过程进行的,并且蛋白质的进化以非马尔可夫方式进行。另一方面,马尔可夫模型是进化研究中许多应用程序的基础。明显的非马尔可夫行为或时间依赖性行为被归因于短时间尺度上遗传密码的影响以及长时间尺度上氨基酸的理化性质的主导。但是,任何长时间段只是许多短时间段的累积,目前尚不清楚为什么进化在所研究的时间范围内应表现出系统的不同作用。我们显示观察到的时间依赖性行为可以通过将蛋白质序列进化建模为聚集马尔可夫过程(AMP)进行定性解释:仅在蛋白质编码DNA编码的氨基酸水平上观察到的时间均质马尔可夫置换模型顺序。 AMPs的研究为氨基酸水平和密码子水平的序列进化模型之间的关系提供了新的思路,我们的结果表明蛋白质进化应该在密码子水平上进行建模,而不是使用氨基酸取代模型。

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