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


Journal

Briefings in bioinformatics
ISSN: 1477-4054
Titre abrégé: Brief Bioinform
Pays: England
ID NLM: 100912837

Informations de publication

Date de publication:
02 09 2021
Historique:
received: 08 01 2021
revised: 17 03 2021
accepted: 26 03 2021
pubmed: 19 4 2021
medline: 23 11 2021
entrez: 18 4 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33866372
pii: 6231751
doi: 10.1093/bib/bbab145
pii:
doi:

Substances chimiques

Intrinsically Disordered Proteins 0
Proteome 0
Viral Proteins 0
RNA, Transfer 9014-25-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : UK Research and Innovation - Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007038

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Naveen Kumar (N)

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

Rahul Kaushik (R)

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

Chandana Tennakoon (C)

The Pirbright Institute, Woking GU24 0NF, UK.

Vladimir N Uversky (VN)

Department of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL 33612, USA.
Institute for Biological Instrumentation of the Russian Academy of Sciences, Federal Research Center 'Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences', Moscow region, Pushchino 142290, Russia.

Sonia Longhi (S)

Aix-Marseille Université and CNRS, Laboratoire Architecture et Fonction des Macromolecules Biologiques (AFMB), UMR 7257, Marseille, France.

Kam Y J Zhang (KYJ)

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

Sandeep Bhatia (S)

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

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