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深入了解塑造编码内在无序蛋白区域的病毒基因组片段中密码子使用偏好的进化力量。

Insights into the evolutionary forces that shape the codon usage in the viral genome segments encoding intrinsically disordered protein regions.

机构信息

Diagnostic & Vaccine Group, ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.

Laboratory for Structural Bioinformatics, Center for Biosystems Dynamics Research, RIKEN, 1-7-22 Suehiro, Yokohama, Kanagawa 230-0045, Japan.

出版信息

Brief Bioinform. 2021 Sep 2;22(5). doi: 10.1093/bib/bbab145.

Abstract

Intrinsically disordered regions/proteins (IDRs) are abundant across all the domains of life, where they perform important regulatory roles and supplement the biological functions of structured proteins/regions (SRs). Despite the multifunctionality features of IDRs, several interrogations on the evolution of viral genomic regions encoding IDRs in diverse viral proteins remain unreciprocated. To fill this gap, we benchmarked the findings of two most widely used and reliable intrinsic disorder prediction algorithms (IUPred2A and ESpritz) to a dataset of 6108 reference viral proteomes to unravel the multifaceted evolutionary forces that shape the codon usage in the viral genomic regions encoding for IDRs and SRs. We found persuasive evidence that the natural selection predominantly governs the evolution of codon usage in regions encoding IDRs by most of the viruses. In addition, we confirm not only that codon usage in regions encoding IDRs is less optimized for the protein synthesis machinery (transfer RNAs pool) of their host than for those encoding SRs, but also that the selective constraints imposed by codon bias sustain this reduced optimization in IDRs. Our analysis also establishes that IDRs in viruses are likely to tolerate more translational errors than SRs. All these findings hold true, irrespective of the disorder prediction algorithms used to classify IDRs. In conclusion, our study offers a novel perspective on the evolution of viral IDRs and the evolutionary adaptability to multiple taxonomically divergent hosts.

摘要

无规卷曲区域/蛋白质(IDR)在所有生命领域都大量存在,它们在其中发挥着重要的调节作用,并补充了结构蛋白/区域(SR)的生物学功能。尽管 IDR 具有多功能性特征,但关于编码 IDR 的病毒基因组区域在不同病毒蛋白中的进化仍有几个问题尚未得到解答。为了填补这一空白,我们将两种最广泛使用和可靠的固有无序预测算法(IUPred2A 和 Espritz)的结果与 6108 个参考病毒蛋白质组数据集进行了基准测试,以揭示塑造编码 IDR 和 SR 的病毒基因组区域中密码子使用的多方面进化力量。我们有充分的证据表明,自然选择主要控制着编码 IDR 的区域的密码子使用的进化。此外,我们不仅证实了编码 IDR 的区域的密码子使用比对其宿主的蛋白质合成机制(转移 RNA 池)的优化程度不如那些编码 SR 的区域,而且由密码子偏倚施加的选择约束维持了 IDR 中这种降低的优化。我们的分析还表明,病毒中的 IDR 比 SR 更能容忍更多的翻译错误。所有这些发现都成立,无论用于分类 IDR 的无序预测算法如何。总之,我们的研究为病毒 IDR 的进化和对多种分类学上不同宿主的进化适应性提供了新的视角。

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