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Highly expressed genes evolve under strong epistasis from a proteome-wide scan in E. coli

机译:高表达基因在大肠杆菌的全蛋白质组扫描中在强上位性下进化

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摘要

Epistasis or the non-additivity of mutational effects is a major force in protein evolution, but it has not been systematically quantified at the level of a proteome. Here, we estimated the extent of epistasis for 2,382 genes in E. coli using several hundreds of orthologs for each gene within the class Gammaproteobacteria. We found that the average epistasis is ~41% across genes in the proteome and that epistasis is stronger among highly expressed genes. This trend is quantitatively explained by the prevailing model of sequence evolution based on minimizing the fitness cost of protein unfolding and aggregation. The genes with the highest epistasis are also functionally involved in the maintenance of proteostasis, translation and central metabolism. In contrast, genes evolving with low epistasis mainly encode for membrane proteins and are involved in transport activity. Our results highlight the coupling between selection and epistasis in the long-term evolution of a proteome.
机译:上位性或突变作用的非可加性是蛋白质进化的主要力量,但尚未在蛋白质组学水平上对其进行系统地定量。在这里,我们使用γ-变形杆菌属中每个基因的数百个直系同源物,估计了大肠杆菌中2,382个基因的上位性程度。我们发现蛋白质组中各个基因的平均上位率为〜41%,而高表达基因中的上位性更强。这种趋势由基于最小化蛋白质展开和聚集的适应性成本的主流序列进化模型进行了定量解释。具有最高上位性的基因在功能上也参与了蛋白稳态,翻译和中枢代谢的维持。相反,具有低上位性的进化基因主要编码膜蛋白,并参与转运活性。我们的结果突出了蛋白质组的长期进化中选择和上位之间的耦合。

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