Insights into the evolutionary forces that shape the codon usage in the viral genome segments encoding intrinsically disordered protein regions.
Algorithms
Codon Usage
/ genetics
Computational Biology
/ methods
CpG Islands
/ genetics
Evolution, Molecular
Genome, Viral
/ genetics
Intrinsically Disordered Proteins
/ genetics
Mutation
Protein Biosynthesis
/ genetics
Protein Processing, Post-Translational
Proteome
/ genetics
Proteomics
/ methods
RNA, Transfer
/ genetics
Reproducibility of Results
Selection, Genetic
Viral Proteins
/ genetics
CpG contents
disorder prediction algorithms
evolutionary forces
intrinsically disordered regions
translation adaptation
viral proteome
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
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.