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启动子活性与编码突变的上位性塑造基因的可进化性。

Epistasis between promoter activity and coding mutations shapes gene evolvability.

机构信息

Département de biochimie, de microbiologie et de bio-informatique, Faculté des sciences et de génie, Université Laval, G1V 0A6, Québec, Canada.

Institut de biologie intégrative et des systèmes, Université Laval, G1V 0A6, Québec, Canada.

出版信息

Sci Adv. 2023 Feb 3;9(5):eadd9109. doi: 10.1126/sciadv.add9109.

Abstract

The evolution of protein-coding genes proceeds as mutations act on two main dimensions: regulation of transcription level and the coding sequence. The extent and impact of the connection between these two dimensions are largely unknown because they have generally been studied independently. By measuring the fitness effects of all possible mutations on a protein complex at various levels of promoter activity, we show that promoter activity at the optimal level for the wild-type protein masks the effects of both deleterious and beneficial coding mutations. Mutations that are deleterious at low activity but masked at optimal activity are slightly destabilizing for individual subunits and binding interfaces. Coding mutations that increase protein abundance are beneficial at low expression but could potentially incur a cost at high promoter activity. We thereby demonstrate that promoter activity in interaction with protein properties can dictate which coding mutations are beneficial, neutral, or deleterious.

摘要

蛋白质编码基因的进化是由突变在两个主要方面起作用的

转录水平的调节和编码序列。这两个维度之间的联系的程度和影响在很大程度上是未知的,因为它们通常是独立研究的。通过测量在不同启动子活性水平下蛋白质复合物上所有可能突变的适合度效应,我们表明,野生型蛋白质的最佳启动子活性掩盖了有害和有益编码突变的影响。在低活性下有害但在最佳活性下被掩盖的突变对单个亚基和结合界面略有不稳定性。增加蛋白质丰度的编码突变在低表达时是有益的,但在高启动子活性时可能会带来代价。因此,我们证明了启动子活性与蛋白质性质的相互作用可以决定哪些编码突变是有益的、中性的或有害的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf8/9897669/a0aec7b5c6be/sciadv.add9109-f1.jpg

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