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Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses

The nucleotide composition, dinucleotide composition, and codon usage of many viruses differ from their hosts. These differences arise because viruses are subject to unique mutation and selection pressures that do not apply to host genomes; however, the molecular mechanisms that underlie these evolu...

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Autores principales: Mordstein, Christine, Cano, Laura, Morales, Atahualpa Castillo, Young, Bethan, Ho, Alexander T, Rice, Alan M, Liss, Michael, Hurst, Laurence D, Kudla, Grzegorz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410142/
https://www.ncbi.nlm.nih.gov/pubmed/33988683
http://dx.doi.org/10.1093/gbe/evab106
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author Mordstein, Christine
Cano, Laura
Morales, Atahualpa Castillo
Young, Bethan
Ho, Alexander T
Rice, Alan M
Liss, Michael
Hurst, Laurence D
Kudla, Grzegorz
author_facet Mordstein, Christine
Cano, Laura
Morales, Atahualpa Castillo
Young, Bethan
Ho, Alexander T
Rice, Alan M
Liss, Michael
Hurst, Laurence D
Kudla, Grzegorz
author_sort Mordstein, Christine
collection PubMed
description The nucleotide composition, dinucleotide composition, and codon usage of many viruses differ from their hosts. These differences arise because viruses are subject to unique mutation and selection pressures that do not apply to host genomes; however, the molecular mechanisms that underlie these evolutionary forces are unclear. Here, we analyzed the patterns of codon usage in 1,520 vertebrate-infecting viruses, focusing on parameters known to be under selection and associated with gene regulation. We find that GC content, dinucleotide content, and splicing and m(6)A modification-related sequence motifs are associated with the type of genetic material (DNA or RNA), strandedness, and replication compartment of viruses. In an experimental follow-up, we find that the effects of GC content on gene expression depend on whether the genetic material is delivered to the cell as DNA or mRNA, whether it is transcribed by endogenous or exogenous RNA polymerase, and whether transcription takes place in the nucleus or cytoplasm. Our results suggest that viral codon usage cannot be explained by a simple adaptation to the codon usage of the host—instead, it reflects the combination of multiple selective and mutational pressures, including the need for efficient transcription, export, and immune evasion.
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spelling pubmed-84101422021-09-02 Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses Mordstein, Christine Cano, Laura Morales, Atahualpa Castillo Young, Bethan Ho, Alexander T Rice, Alan M Liss, Michael Hurst, Laurence D Kudla, Grzegorz Genome Biol Evol Research Article The nucleotide composition, dinucleotide composition, and codon usage of many viruses differ from their hosts. These differences arise because viruses are subject to unique mutation and selection pressures that do not apply to host genomes; however, the molecular mechanisms that underlie these evolutionary forces are unclear. Here, we analyzed the patterns of codon usage in 1,520 vertebrate-infecting viruses, focusing on parameters known to be under selection and associated with gene regulation. We find that GC content, dinucleotide content, and splicing and m(6)A modification-related sequence motifs are associated with the type of genetic material (DNA or RNA), strandedness, and replication compartment of viruses. In an experimental follow-up, we find that the effects of GC content on gene expression depend on whether the genetic material is delivered to the cell as DNA or mRNA, whether it is transcribed by endogenous or exogenous RNA polymerase, and whether transcription takes place in the nucleus or cytoplasm. Our results suggest that viral codon usage cannot be explained by a simple adaptation to the codon usage of the host—instead, it reflects the combination of multiple selective and mutational pressures, including the need for efficient transcription, export, and immune evasion. Oxford University Press 2021-05-14 /pmc/articles/PMC8410142/ /pubmed/33988683 http://dx.doi.org/10.1093/gbe/evab106 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mordstein, Christine
Cano, Laura
Morales, Atahualpa Castillo
Young, Bethan
Ho, Alexander T
Rice, Alan M
Liss, Michael
Hurst, Laurence D
Kudla, Grzegorz
Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title_full Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title_fullStr Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title_full_unstemmed Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title_short Transcription, mRNA Export, and Immune Evasion Shape the Codon Usage of Viruses
title_sort transcription, mrna export, and immune evasion shape the codon usage of viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410142/
https://www.ncbi.nlm.nih.gov/pubmed/33988683
http://dx.doi.org/10.1093/gbe/evab106
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