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On Ribosome Load, Codon Bias and Protein Abundance
Different codons encoding the same amino acid are not used equally in protein-coding sequences. In bacteria, there is a bias towards codons with high translation rates. This bias is most pronounced in highly expressed proteins, but a recent study of synthetic GFP-coding sequences did not find a corr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492488/ https://www.ncbi.nlm.nih.gov/pubmed/23144899 http://dx.doi.org/10.1371/journal.pone.0048542 |
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author | Klumpp, Stefan Dong, Jiajia Hwa, Terence |
author_facet | Klumpp, Stefan Dong, Jiajia Hwa, Terence |
author_sort | Klumpp, Stefan |
collection | PubMed |
description | Different codons encoding the same amino acid are not used equally in protein-coding sequences. In bacteria, there is a bias towards codons with high translation rates. This bias is most pronounced in highly expressed proteins, but a recent study of synthetic GFP-coding sequences did not find a correlation between codon usage and GFP expression, suggesting that such correlation in natural sequences is not a simple property of translational mechanisms. Here, we investigate the effect of evolutionary forces on codon usage. The relation between codon bias and protein abundance is quantitatively analyzed based on the hypothesis that codon bias evolved to ensure the efficient usage of ribosomes, a precious commodity for fast growing cells. An explicit fitness landscape is formulated based on bacterial growth laws to relate protein abundance and ribosomal load. The model leads to a quantitative relation between codon bias and protein abundance, which accounts for a substantial part of the observed bias for E. coli. Moreover, by providing an evolutionary link, the ribosome load model resolves the apparent conflict between the observed relation of protein abundance and codon bias in natural sequences and the lack of such dependence in a synthetic gfp library. Finally, we show that the relation between codon usage and protein abundance can be used to predict protein abundance from genomic sequence data alone without adjustable parameters. |
format | Online Article Text |
id | pubmed-3492488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34924882012-11-09 On Ribosome Load, Codon Bias and Protein Abundance Klumpp, Stefan Dong, Jiajia Hwa, Terence PLoS One Research Article Different codons encoding the same amino acid are not used equally in protein-coding sequences. In bacteria, there is a bias towards codons with high translation rates. This bias is most pronounced in highly expressed proteins, but a recent study of synthetic GFP-coding sequences did not find a correlation between codon usage and GFP expression, suggesting that such correlation in natural sequences is not a simple property of translational mechanisms. Here, we investigate the effect of evolutionary forces on codon usage. The relation between codon bias and protein abundance is quantitatively analyzed based on the hypothesis that codon bias evolved to ensure the efficient usage of ribosomes, a precious commodity for fast growing cells. An explicit fitness landscape is formulated based on bacterial growth laws to relate protein abundance and ribosomal load. The model leads to a quantitative relation between codon bias and protein abundance, which accounts for a substantial part of the observed bias for E. coli. Moreover, by providing an evolutionary link, the ribosome load model resolves the apparent conflict between the observed relation of protein abundance and codon bias in natural sequences and the lack of such dependence in a synthetic gfp library. Finally, we show that the relation between codon usage and protein abundance can be used to predict protein abundance from genomic sequence data alone without adjustable parameters. Public Library of Science 2012-11-07 /pmc/articles/PMC3492488/ /pubmed/23144899 http://dx.doi.org/10.1371/journal.pone.0048542 Text en © 2012 Klumpp 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 Klumpp, Stefan Dong, Jiajia Hwa, Terence On Ribosome Load, Codon Bias and Protein Abundance |
title | On Ribosome Load, Codon Bias and Protein Abundance |
title_full | On Ribosome Load, Codon Bias and Protein Abundance |
title_fullStr | On Ribosome Load, Codon Bias and Protein Abundance |
title_full_unstemmed | On Ribosome Load, Codon Bias and Protein Abundance |
title_short | On Ribosome Load, Codon Bias and Protein Abundance |
title_sort | on ribosome load, codon bias and protein abundance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492488/ https://www.ncbi.nlm.nih.gov/pubmed/23144899 http://dx.doi.org/10.1371/journal.pone.0048542 |
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