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在低表达水平下揭示 Hsp90 突变体的潜在效应。

Latent effects of Hsp90 mutants revealed at reduced expression levels.

机构信息

Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

PLoS Genet. 2013 Jun;9(6):e1003600. doi: 10.1371/journal.pgen.1003600. Epub 2013 Jun 27.

Abstract

In natural systems, selection acts on both protein sequence and expression level, but it is unclear how selection integrates over these two dimensions. We recently developed the EMPIRIC approach to systematically determine the fitness effects of all possible point mutants for important regions of essential genes in yeast. Here, we systematically investigated the fitness effects of point mutations in a putative substrate binding loop of yeast Hsp90 (Hsp82) over a broad range of expression strengths. Negative epistasis between reduced expression strength and amino acid substitutions was common, and the endogenous expression strength frequently obscured mutant defects. By analyzing fitness effects at varied expression strengths, we were able to uncover all mutant effects on function. The majority of mutants caused partial functional defects, consistent with this region of Hsp90 contributing to a mutation sensitive and critical process. These results demonstrate that important functional regions of proteins can tolerate mutational defects without experimentally observable impacts on fitness.

摘要

在自然系统中,选择既作用于蛋白质序列,又作用于表达水平,但目前尚不清楚选择如何在这两个维度上进行整合。我们最近开发了 EMPIRIC 方法,用于系统地确定酵母中重要必需基因区域的所有可能点突变的适应度效应。在这里,我们系统地研究了酵母 Hsp90(Hsp82)中一个假定的底物结合环的点突变在广泛的表达强度下的适应度效应。降低表达强度与氨基酸取代之间的负遗传相互作用很常见,内源性表达强度经常掩盖了突变缺陷。通过分析不同表达强度下的适应度效应,我们能够揭示该功能区域中所有突变对功能的影响。大多数突变导致部分功能缺陷,这与该 Hsp90 区域对敏感和关键过程的突变有关。这些结果表明,蛋白质的重要功能区域可以容忍突变缺陷,而不会对适应度产生实验上可观察到的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5430/3694843/3f0d4ef66c3c/pgen.1003600.g001.jpg

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