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Widespread position-specific conservation of synonymous rare codons within coding sequences

Synonymous rare codons are considered to be sub-optimal for gene expression because they are translated more slowly than common codons. Yet surprisingly, many protein coding sequences include large clusters of synonymous rare codons. Rare codons at the 5’ terminus of coding sequences have been shown...

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Autores principales: Chaney, Julie L., Steele, Aaron, Carmichael, Rory, Rodriguez, Anabel, Specht, Alicia T., Ngo, Kim, Li, Jun, Emrich, Scott, Clark, Patricia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438181/
https://www.ncbi.nlm.nih.gov/pubmed/28475588
http://dx.doi.org/10.1371/journal.pcbi.1005531
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author Chaney, Julie L.
Steele, Aaron
Carmichael, Rory
Rodriguez, Anabel
Specht, Alicia T.
Ngo, Kim
Li, Jun
Emrich, Scott
Clark, Patricia L.
author_facet Chaney, Julie L.
Steele, Aaron
Carmichael, Rory
Rodriguez, Anabel
Specht, Alicia T.
Ngo, Kim
Li, Jun
Emrich, Scott
Clark, Patricia L.
author_sort Chaney, Julie L.
collection PubMed
description Synonymous rare codons are considered to be sub-optimal for gene expression because they are translated more slowly than common codons. Yet surprisingly, many protein coding sequences include large clusters of synonymous rare codons. Rare codons at the 5’ terminus of coding sequences have been shown to increase translational efficiency. Although a general functional role for synonymous rare codons farther within coding sequences has not yet been established, several recent reports have identified rare-to-common synonymous codon substitutions that impair folding of the encoded protein. Here we test the hypothesis that although the usage frequencies of synonymous codons change from organism to organism, codon rarity will be conserved at specific positions in a set of homologous coding sequences, for example to tune translation rate without altering a protein sequence. Such conservation of rarity–rather than specific codon identity–could coordinate co-translational folding of the encoded protein. We demonstrate that many rare codon cluster positions are indeed conserved within homologous coding sequences across diverse eukaryotic, bacterial, and archaeal species, suggesting they result from positive selection and have a functional role. Most conserved rare codon clusters occur within rather than between conserved protein domains, challenging the view that their primary function is to facilitate co-translational folding after synthesis of an autonomous structural unit. Instead, many conserved rare codon clusters separate smaller protein structural motifs within structural domains. These smaller motifs typically fold faster than an entire domain, on a time scale more consistent with translation rate modulation by synonymous codon usage. While proteins with conserved rare codon clusters are structurally and functionally diverse, they are enriched in functions associated with organism growth and development, suggesting an important role for synonymous codon usage in organism physiology. The identification of conserved rare codon clusters advances our understanding of distinct, functional roles for otherwise synonymous codons and enables experimental testing of the impact of synonymous codon usage on the production of functional proteins.
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spelling pubmed-54381812017-05-26 Widespread position-specific conservation of synonymous rare codons within coding sequences Chaney, Julie L. Steele, Aaron Carmichael, Rory Rodriguez, Anabel Specht, Alicia T. Ngo, Kim Li, Jun Emrich, Scott Clark, Patricia L. PLoS Comput Biol Research Article Synonymous rare codons are considered to be sub-optimal for gene expression because they are translated more slowly than common codons. Yet surprisingly, many protein coding sequences include large clusters of synonymous rare codons. Rare codons at the 5’ terminus of coding sequences have been shown to increase translational efficiency. Although a general functional role for synonymous rare codons farther within coding sequences has not yet been established, several recent reports have identified rare-to-common synonymous codon substitutions that impair folding of the encoded protein. Here we test the hypothesis that although the usage frequencies of synonymous codons change from organism to organism, codon rarity will be conserved at specific positions in a set of homologous coding sequences, for example to tune translation rate without altering a protein sequence. Such conservation of rarity–rather than specific codon identity–could coordinate co-translational folding of the encoded protein. We demonstrate that many rare codon cluster positions are indeed conserved within homologous coding sequences across diverse eukaryotic, bacterial, and archaeal species, suggesting they result from positive selection and have a functional role. Most conserved rare codon clusters occur within rather than between conserved protein domains, challenging the view that their primary function is to facilitate co-translational folding after synthesis of an autonomous structural unit. Instead, many conserved rare codon clusters separate smaller protein structural motifs within structural domains. These smaller motifs typically fold faster than an entire domain, on a time scale more consistent with translation rate modulation by synonymous codon usage. While proteins with conserved rare codon clusters are structurally and functionally diverse, they are enriched in functions associated with organism growth and development, suggesting an important role for synonymous codon usage in organism physiology. The identification of conserved rare codon clusters advances our understanding of distinct, functional roles for otherwise synonymous codons and enables experimental testing of the impact of synonymous codon usage on the production of functional proteins. Public Library of Science 2017-05-05 /pmc/articles/PMC5438181/ /pubmed/28475588 http://dx.doi.org/10.1371/journal.pcbi.1005531 Text en © 2017 Chaney 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chaney, Julie L.
Steele, Aaron
Carmichael, Rory
Rodriguez, Anabel
Specht, Alicia T.
Ngo, Kim
Li, Jun
Emrich, Scott
Clark, Patricia L.
Widespread position-specific conservation of synonymous rare codons within coding sequences
title Widespread position-specific conservation of synonymous rare codons within coding sequences
title_full Widespread position-specific conservation of synonymous rare codons within coding sequences
title_fullStr Widespread position-specific conservation of synonymous rare codons within coding sequences
title_full_unstemmed Widespread position-specific conservation of synonymous rare codons within coding sequences
title_short Widespread position-specific conservation of synonymous rare codons within coding sequences
title_sort widespread position-specific conservation of synonymous rare codons within coding sequences
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438181/
https://www.ncbi.nlm.nih.gov/pubmed/28475588
http://dx.doi.org/10.1371/journal.pcbi.1005531
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