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从经验证据看错误折叠避免假说与蛋白质进化速率的关系。

The Relationship between the Misfolding Avoidance Hypothesis and Protein Evolutionary Rates in the Light of Empirical Evidence.

机构信息

Department of Systems Biology, Columbia University, New York, NY, USA.

Elanco Animal Health, Greenfield, IN, USA.

出版信息

Genome Biol Evol. 2021 Feb 3;13(2). doi: 10.1093/gbe/evab006.

Abstract

For more than a decade, the misfolding avoidance hypothesis (MAH) and related theories have dominated evolutionary discussions aimed at explaining the variance of the molecular clock across cellular proteins. In this study, we use various experimental data to further investigate the consistency of the MAH predictions with empirical evidence. We also critically discuss experimental results that motivated the MAH development and that are often viewed as evidence of its major contribution to the variability of protein evolutionary rates. We demonstrate, in Escherichia coli and Homo sapiens, the lack of a substantial negative correlation between protein evolutionary rates and Gibbs free energies of unfolding, a direct measure of protein stability. We then analyze multiple new genome-scale data sets characterizing protein aggregation and interaction propensities, the properties that are likely optimized in evolution to alleviate deleterious effects associated with toxic protein misfolding and misinteractions. Our results demonstrate that the propensity of proteins to aggregate, the fraction of charged amino acids, and protein stickiness do correlate with protein abundances. Nevertheless, across multiple organisms and various data sets we do not observe substantial correlations between proteins' aggregation- and stability-related properties and evolutionary rates. Therefore, diverse empirical data support the conclusion that the MAH and similar hypotheses do not play a major role in mediating a strong negative correlation between protein expression and the molecular clock, and thus in explaining the variability of evolutionary rates across cellular proteins.

摘要

十多年来,错误折叠避免假说(MAH)和相关理论一直主导着旨在解释细胞蛋白中分子钟变化的进化讨论。在这项研究中,我们使用各种实验数据进一步研究 MAH 预测与经验证据的一致性。我们还批判性地讨论了激发 MAH 发展的实验结果,这些结果通常被视为其对蛋白质进化率可变性的主要贡献的证据。我们在大肠杆菌和人类中证明,蛋白质进化率与解折叠吉布斯自由能之间没有实质性的负相关,而解折叠吉布斯自由能是蛋白质稳定性的直接衡量标准。然后,我们分析了多个新的基因组规模数据集,这些数据集描述了蛋白质聚集和相互作用倾向,这些特性很可能在进化中得到优化,以减轻与毒性蛋白质错误折叠和错误相互作用相关的有害影响。我们的研究结果表明,蛋白质聚集的倾向、带电荷氨基酸的分数和蛋白质粘性与蛋白质丰度相关。然而,在多个生物体和各种数据集上,我们没有观察到蛋白质聚集和稳定性相关特性与进化率之间存在实质性的相关性。因此,多样化的经验数据支持这样的结论:MAH 和类似的假说并没有在介导蛋白质表达与分子钟之间的强负相关以及解释细胞蛋白中进化率的可变性方面发挥主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f50d/7874998/60d4e00d37b3/evab006f1.jpg

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