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Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses

Prasinoviruses are among the largest viruses (>200 kb) and encode several hundreds of protein coding genes, including most genes of the DNA replication machinery and several genes involved in transcription and translation, as well as transfer RNAs (tRNAs). They can infect and lyse small eukaryoti...

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Autores principales: Michely, Stephanie, Toulza, Eve, Subirana, Lucie, John, Uwe, Cognat, Valérie, Maréchal-Drouard, Laurence, Grimsley, Nigel, Moreau, Hervé, Piganeau, Gwenaël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673656/
https://www.ncbi.nlm.nih.gov/pubmed/23563969
http://dx.doi.org/10.1093/gbe/evt053
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author Michely, Stephanie
Toulza, Eve
Subirana, Lucie
John, Uwe
Cognat, Valérie
Maréchal-Drouard, Laurence
Grimsley, Nigel
Moreau, Hervé
Piganeau, Gwenaël
author_facet Michely, Stephanie
Toulza, Eve
Subirana, Lucie
John, Uwe
Cognat, Valérie
Maréchal-Drouard, Laurence
Grimsley, Nigel
Moreau, Hervé
Piganeau, Gwenaël
author_sort Michely, Stephanie
collection PubMed
description Prasinoviruses are among the largest viruses (>200 kb) and encode several hundreds of protein coding genes, including most genes of the DNA replication machinery and several genes involved in transcription and translation, as well as transfer RNAs (tRNAs). They can infect and lyse small eukaryotic planktonic marine green algae, thereby affecting global algal population dynamics. Here, we investigate the causes of codon usage bias (CUB) in one prasinovirus, OtV5, and its host Ostreococcus tauri, during a viral infection using microarray expression data. We show that 1) CUB in the host and in the viral genes increases with expression levels and 2) optimal codons use those tRNAs encoded by the most abundant host tRNA genes, supporting the notion of translational optimization by natural selection. We find evidence that viral tRNA genes complement the host tRNA pool for those viral amino acids whose host tRNAs are in short supply. We further discuss the coevolution of CUB in hosts and prasinoviruses by comparing optimal codons in three evolutionary diverged host–virus-specific pairs whose complete genome sequences are known.
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spelling pubmed-36736562013-06-05 Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses Michely, Stephanie Toulza, Eve Subirana, Lucie John, Uwe Cognat, Valérie Maréchal-Drouard, Laurence Grimsley, Nigel Moreau, Hervé Piganeau, Gwenaël Genome Biol Evol Research Article Prasinoviruses are among the largest viruses (>200 kb) and encode several hundreds of protein coding genes, including most genes of the DNA replication machinery and several genes involved in transcription and translation, as well as transfer RNAs (tRNAs). They can infect and lyse small eukaryotic planktonic marine green algae, thereby affecting global algal population dynamics. Here, we investigate the causes of codon usage bias (CUB) in one prasinovirus, OtV5, and its host Ostreococcus tauri, during a viral infection using microarray expression data. We show that 1) CUB in the host and in the viral genes increases with expression levels and 2) optimal codons use those tRNAs encoded by the most abundant host tRNA genes, supporting the notion of translational optimization by natural selection. We find evidence that viral tRNA genes complement the host tRNA pool for those viral amino acids whose host tRNAs are in short supply. We further discuss the coevolution of CUB in hosts and prasinoviruses by comparing optimal codons in three evolutionary diverged host–virus-specific pairs whose complete genome sequences are known. Oxford University Press 2013 2013-04-05 /pmc/articles/PMC3673656/ /pubmed/23563969 http://dx.doi.org/10.1093/gbe/evt053 Text en © The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Michely, Stephanie
Toulza, Eve
Subirana, Lucie
John, Uwe
Cognat, Valérie
Maréchal-Drouard, Laurence
Grimsley, Nigel
Moreau, Hervé
Piganeau, Gwenaël
Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title_full Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title_fullStr Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title_full_unstemmed Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title_short Evolution of Codon Usage in the Smallest Photosynthetic Eukaryotes and Their Giant Viruses
title_sort evolution of codon usage in the smallest photosynthetic eukaryotes and their giant viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673656/
https://www.ncbi.nlm.nih.gov/pubmed/23563969
http://dx.doi.org/10.1093/gbe/evt053
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