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Codon usage variability determines the correlation between proteome and transcriptome fold changes
BACKGROUND: The availability of high throughput experimental methods has made possible to observe the relationships between proteome and transcirptome. The protein abundances show a positive but weak correlation with the concentrations of their cognate mRNAs. This weak correlation implies that there...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058016/ https://www.ncbi.nlm.nih.gov/pubmed/21352515 http://dx.doi.org/10.1186/1752-0509-5-33 |
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author | Olivares-Hernández, Roberto Bordel, Sergio Nielsen, Jens |
author_facet | Olivares-Hernández, Roberto Bordel, Sergio Nielsen, Jens |
author_sort | Olivares-Hernández, Roberto |
collection | PubMed |
description | BACKGROUND: The availability of high throughput experimental methods has made possible to observe the relationships between proteome and transcirptome. The protein abundances show a positive but weak correlation with the concentrations of their cognate mRNAs. This weak correlation implies that there are other crucial effects involved in the regulation of protein translation, different from the sole availability of mRNA. It is well known that ribosome and tRNA concentrations are sources of variation in protein levels. Thus, by using integrated analysis of omics data, genomic information, transcriptome and proteome, we aim to unravel important variables affecting translation. RESULTS: We identified how much of the variability in the correlation between protein and mRNA concentrations can be attributed to the gene codon frequencies. We propose the hypothesis that the influence of codon frequency is due to the competition of cognate and near-cognate tRNA binding; which in turn is a function of the tRNA concentrations. Transcriptome and proteome data were combined in two analytical steps; first, we used Self-Organizing Maps (SOM) to identify similarities among genes, based on their codon frequencies, grouping them into different clusters; and second, we calculated the variance in the protein mRNA correlation in the sampled genes from each cluster. This procedure is justified within a mathematical framework. CONCLUSIONS: With the proposed method we observed that in all the six studied cases most of the variability in the relation protein-transcript could be explained by the variation in codon composition. |
format | Text |
id | pubmed-3058016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30580162011-03-17 Codon usage variability determines the correlation between proteome and transcriptome fold changes Olivares-Hernández, Roberto Bordel, Sergio Nielsen, Jens BMC Syst Biol Research Article BACKGROUND: The availability of high throughput experimental methods has made possible to observe the relationships between proteome and transcirptome. The protein abundances show a positive but weak correlation with the concentrations of their cognate mRNAs. This weak correlation implies that there are other crucial effects involved in the regulation of protein translation, different from the sole availability of mRNA. It is well known that ribosome and tRNA concentrations are sources of variation in protein levels. Thus, by using integrated analysis of omics data, genomic information, transcriptome and proteome, we aim to unravel important variables affecting translation. RESULTS: We identified how much of the variability in the correlation between protein and mRNA concentrations can be attributed to the gene codon frequencies. We propose the hypothesis that the influence of codon frequency is due to the competition of cognate and near-cognate tRNA binding; which in turn is a function of the tRNA concentrations. Transcriptome and proteome data were combined in two analytical steps; first, we used Self-Organizing Maps (SOM) to identify similarities among genes, based on their codon frequencies, grouping them into different clusters; and second, we calculated the variance in the protein mRNA correlation in the sampled genes from each cluster. This procedure is justified within a mathematical framework. CONCLUSIONS: With the proposed method we observed that in all the six studied cases most of the variability in the relation protein-transcript could be explained by the variation in codon composition. BioMed Central 2011-02-25 /pmc/articles/PMC3058016/ /pubmed/21352515 http://dx.doi.org/10.1186/1752-0509-5-33 Text en Copyright ©2011 Olivares-Hernández et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Olivares-Hernández, Roberto Bordel, Sergio Nielsen, Jens Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title | Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title_full | Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title_fullStr | Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title_full_unstemmed | Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title_short | Codon usage variability determines the correlation between proteome and transcriptome fold changes |
title_sort | codon usage variability determines the correlation between proteome and transcriptome fold changes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058016/ https://www.ncbi.nlm.nih.gov/pubmed/21352515 http://dx.doi.org/10.1186/1752-0509-5-33 |
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