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Global and gene-specific translational regulation in Escherichia coli across different conditions
How well mRNA transcript levels represent protein abundances has been a controversial issue. Particularly across different environments, correlations between mRNA and protein exhibit remarkable variability from gene to gene. Translational regulation is likely to be one of the key factors contributin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624429/ https://www.ncbi.nlm.nih.gov/pubmed/36264977 http://dx.doi.org/10.1371/journal.pcbi.1010641 |
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author | Zhang, Di Li, Sophia Hsin-Jung King, Christopher G. Wingreen, Ned S. Gitai, Zemer Li, Zhiyuan |
author_facet | Zhang, Di Li, Sophia Hsin-Jung King, Christopher G. Wingreen, Ned S. Gitai, Zemer Li, Zhiyuan |
author_sort | Zhang, Di |
collection | PubMed |
description | How well mRNA transcript levels represent protein abundances has been a controversial issue. Particularly across different environments, correlations between mRNA and protein exhibit remarkable variability from gene to gene. Translational regulation is likely to be one of the key factors contributing to mismatches between mRNA level and protein abundance in bacteria. Here, we quantified genome-wide transcriptome and relative translation efficiency (RTE) under 12 different conditions in Escherichia coli. By quantifying the mRNA-RTE correlation both across genes and across conditions, we uncovered a diversity of gene-specific translational regulations, cooperating with transcriptional regulations, in response to carbon (C), nitrogen (N), and phosphate (P) limitations. Intriguingly, we found that many genes regulating translation are themselves subject to translational regulation, suggesting possible feedbacks. Furthermore, a random forest model suggests that codon usage partially predicts a gene’s cross-condition variability in translation efficiency; such cross-condition variability tends to be an inherent quality of a gene, independent of the specific nutrient limitations. These findings broaden the understanding of translational regulation under different environments and provide novel strategies for the control of translation in synthetic biology. In addition, our data offers a resource for future multi-omics studies. |
format | Online Article Text |
id | pubmed-9624429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96244292022-11-02 Global and gene-specific translational regulation in Escherichia coli across different conditions Zhang, Di Li, Sophia Hsin-Jung King, Christopher G. Wingreen, Ned S. Gitai, Zemer Li, Zhiyuan PLoS Comput Biol Research Article How well mRNA transcript levels represent protein abundances has been a controversial issue. Particularly across different environments, correlations between mRNA and protein exhibit remarkable variability from gene to gene. Translational regulation is likely to be one of the key factors contributing to mismatches between mRNA level and protein abundance in bacteria. Here, we quantified genome-wide transcriptome and relative translation efficiency (RTE) under 12 different conditions in Escherichia coli. By quantifying the mRNA-RTE correlation both across genes and across conditions, we uncovered a diversity of gene-specific translational regulations, cooperating with transcriptional regulations, in response to carbon (C), nitrogen (N), and phosphate (P) limitations. Intriguingly, we found that many genes regulating translation are themselves subject to translational regulation, suggesting possible feedbacks. Furthermore, a random forest model suggests that codon usage partially predicts a gene’s cross-condition variability in translation efficiency; such cross-condition variability tends to be an inherent quality of a gene, independent of the specific nutrient limitations. These findings broaden the understanding of translational regulation under different environments and provide novel strategies for the control of translation in synthetic biology. In addition, our data offers a resource for future multi-omics studies. Public Library of Science 2022-10-20 /pmc/articles/PMC9624429/ /pubmed/36264977 http://dx.doi.org/10.1371/journal.pcbi.1010641 Text en © 2022 Zhang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Zhang, Di Li, Sophia Hsin-Jung King, Christopher G. Wingreen, Ned S. Gitai, Zemer Li, Zhiyuan Global and gene-specific translational regulation in Escherichia coli across different conditions |
title | Global and gene-specific translational regulation in Escherichia coli across different conditions |
title_full | Global and gene-specific translational regulation in Escherichia coli across different conditions |
title_fullStr | Global and gene-specific translational regulation in Escherichia coli across different conditions |
title_full_unstemmed | Global and gene-specific translational regulation in Escherichia coli across different conditions |
title_short | Global and gene-specific translational regulation in Escherichia coli across different conditions |
title_sort | global and gene-specific translational regulation in escherichia coli across different conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624429/ https://www.ncbi.nlm.nih.gov/pubmed/36264977 http://dx.doi.org/10.1371/journal.pcbi.1010641 |
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