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Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency

Cellular efficiency in protein translation is an important fitness determinant in rapidly growing organisms. It is widely believed that synonymous codons are translated with unequal speeds and that translational efficiency is maximized by the exclusive use of rapidly translated codons. Here we estim...

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Autores principales: Qian, Wenfeng, Yang, Jian-Rong, Pearson, Nathaniel M., Maclean, Calum, Zhang, Jianzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315465/
https://www.ncbi.nlm.nih.gov/pubmed/22479199
http://dx.doi.org/10.1371/journal.pgen.1002603
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author Qian, Wenfeng
Yang, Jian-Rong
Pearson, Nathaniel M.
Maclean, Calum
Zhang, Jianzhi
author_facet Qian, Wenfeng
Yang, Jian-Rong
Pearson, Nathaniel M.
Maclean, Calum
Zhang, Jianzhi
author_sort Qian, Wenfeng
collection PubMed
description Cellular efficiency in protein translation is an important fitness determinant in rapidly growing organisms. It is widely believed that synonymous codons are translated with unequal speeds and that translational efficiency is maximized by the exclusive use of rapidly translated codons. Here we estimate the in vivo translational speeds of all sense codons from the budding yeast Saccharomyces cerevisiae. Surprisingly, preferentially used codons are not translated faster than unpreferred ones. We hypothesize that this phenomenon is a result of codon usage in proportion to cognate tRNA concentrations, the optimal strategy in enhancing translational efficiency under tRNA shortage. Our predicted codon–tRNA balance is indeed observed from all model eukaryotes examined, and its impact on translational efficiency is further validated experimentally. Our study reveals a previously unsuspected mechanism by which unequal codon usage increases translational efficiency, demonstrates widespread natural selection for translational efficiency, and offers new strategies to improve synthetic biology.
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spelling pubmed-33154652012-04-04 Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency Qian, Wenfeng Yang, Jian-Rong Pearson, Nathaniel M. Maclean, Calum Zhang, Jianzhi PLoS Genet Research Article Cellular efficiency in protein translation is an important fitness determinant in rapidly growing organisms. It is widely believed that synonymous codons are translated with unequal speeds and that translational efficiency is maximized by the exclusive use of rapidly translated codons. Here we estimate the in vivo translational speeds of all sense codons from the budding yeast Saccharomyces cerevisiae. Surprisingly, preferentially used codons are not translated faster than unpreferred ones. We hypothesize that this phenomenon is a result of codon usage in proportion to cognate tRNA concentrations, the optimal strategy in enhancing translational efficiency under tRNA shortage. Our predicted codon–tRNA balance is indeed observed from all model eukaryotes examined, and its impact on translational efficiency is further validated experimentally. Our study reveals a previously unsuspected mechanism by which unequal codon usage increases translational efficiency, demonstrates widespread natural selection for translational efficiency, and offers new strategies to improve synthetic biology. Public Library of Science 2012-03-29 /pmc/articles/PMC3315465/ /pubmed/22479199 http://dx.doi.org/10.1371/journal.pgen.1002603 Text en Qian et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Qian, Wenfeng
Yang, Jian-Rong
Pearson, Nathaniel M.
Maclean, Calum
Zhang, Jianzhi
Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title_full Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title_fullStr Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title_full_unstemmed Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title_short Balanced Codon Usage Optimizes Eukaryotic Translational Efficiency
title_sort balanced codon usage optimizes eukaryotic translational efficiency
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315465/
https://www.ncbi.nlm.nih.gov/pubmed/22479199
http://dx.doi.org/10.1371/journal.pgen.1002603
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