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Molecular function limits divergent protein evolution on planetary timescales

机译:分子功能限制了行星时间尺度上不同的蛋白质进化

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摘要

Functional conservation is known to constrain protein evolution. Nevertheless, the long-term divergence patterns of proteins maintaining the same molecular function and the possible limits of this divergence have not been explored in detail. We investigate these fundamental questions by characterizing the divergence between ancient protein orthologs with conserved molecular function. Our results demonstrate that the decline of sequence and structural similarities between such orthologs significantly slows down after ~1–2 billion years of independent evolution. As a result, the sequence and structural similarities between ancient orthologs have not substantially decreased for the past billion years. The effective divergence limit (>25% sequence identity) is not primarily due to protein sites universally conserved in all linages. Instead, less than four amino acid types are accepted, on average, per site across orthologous protein sequences. Our analysis also reveals different divergence patterns for protein sites with experimentally determined small and large fitness effects of mutations.>Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed ().
机译:已知功能保守会限制蛋白质的进化。然而,尚未详细探讨维持相同分子功能的蛋白质的长期差异模式以及这种差异的可能限制。我们通过表征具有保守分子功能的古代蛋白质直系同源物之间的差异来研究这些基本问题。我们的结果表明,这种直向同源物之间的序列和结构相似性的下降在约1-20亿年的独立进化后显着减慢了速度。结果,在过去的十亿年中,古代直系同源物之间的序列和结构相似性并未显着降低。有效的差异极限(> 25%的序列同一性)并非主要是由于在所有线性蛋白中普遍保守的蛋白质位点。取而代之,直系同源蛋白质序列中每个位点平均接受少于四种氨基酸类型。我们的分析还揭示了具有实验确定的突变的大小适应性效应的蛋白质位点的不同发散模式。>编者注:本文是通过编辑过程进行的,作者在其中决定如何应对这些问题。在同行评审中提出。审核编辑的评估是,所有问题都已解决()。

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