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大效应有益同义突变介导细菌的快速平行适应

Large-Effect Beneficial Synonymous Mutations Mediate Rapid and Parallel Adaptation in a Bacterium.

作者信息

Agashe Deepa, Sane Mrudula, Phalnikar Kruttika, Diwan Gaurav D, Habibullah Alefiyah, Martinez-Gomez Norma Cecilia, Sahasrabuddhe Vinaya, Polachek William, Wang Jue, Chubiz Lon M, Marx Christopher J

机构信息

National Center for Biological Sciences, Tata Institute of Fundamental Research, GKVK, Bangalore, India Department of Organismic and Evolutionary Biology, Harvard University

National Center for Biological Sciences, Tata Institute of Fundamental Research, GKVK, Bangalore, India.

出版信息

Mol Biol Evol. 2016 Jun;33(6):1542-53. doi: 10.1093/molbev/msw035. Epub 2016 Feb 23.

Abstract

Contrary to previous understanding, recent evidence indicates that synonymous codon changes may sometimes face strong selection. However, it remains difficult to generalize the nature, strength, and mechanism(s) of such selection. Previously, we showed that synonymous variants of a key enzyme-coding gene (fae) of Methylobacterium extorquens AM1 decreased enzyme production and reduced fitness dramatically. We now show that during laboratory evolution, these variants rapidly regained fitness via parallel yet variant-specific, highly beneficial point mutations in the N-terminal region of fae These mutations (including four synonymous mutations) had weak but consistently positive impacts on transcript levels, enzyme production, or enzyme activity. However, none of the proposed mechanisms (including internal ribosome pause sites or mRNA structure) predicted the fitness impact of evolved or additional, engineered point mutations. This study shows that synonymous mutations can be fixed through strong positive selection, but the mechanism for their benefit varies depending on the local sequence context.

摘要

与之前的认识相反,最近的证据表明同义密码子变化有时可能面临强烈的选择。然而,要概括这种选择的性质、强度和机制仍然很困难。此前,我们发现嗜甲基菌AM1关键酶编码基因(fae)的同义变体降低了酶的产生,并显著降低了适应性。我们现在表明,在实验室进化过程中,这些变体通过fae基因N端区域平行但特定于变体的高度有益点突变迅速恢复了适应性。这些突变(包括四个同义突变)对转录水平、酶产生或酶活性有微弱但持续的正向影响。然而,任何提出的机制(包括内部核糖体暂停位点或mRNA结构)都无法预测进化的或额外的工程点突变对适应性的影响。这项研究表明,同义突变可以通过强烈的正选择固定下来,但其有益机制因局部序列背景而异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9f6/4868122/5ceaca5b11c8/msw035f1p.jpg

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