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Genomewide landscape of gene–metabolome associations in Escherichia coli
Metabolism is one of the best‐understood cellular processes whose network topology of enzymatic reactions is determined by an organism's genome. The influence of genes on metabolite levels, however, remains largely unknown, particularly for the many genes encoding non‐enzymatic proteins. Serend...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293155/ https://www.ncbi.nlm.nih.gov/pubmed/28093455 http://dx.doi.org/10.15252/msb.20167150 |
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author | Fuhrer, Tobias Zampieri, Mattia Sévin, Daniel C Sauer, Uwe Zamboni, Nicola |
author_facet | Fuhrer, Tobias Zampieri, Mattia Sévin, Daniel C Sauer, Uwe Zamboni, Nicola |
author_sort | Fuhrer, Tobias |
collection | PubMed |
description | Metabolism is one of the best‐understood cellular processes whose network topology of enzymatic reactions is determined by an organism's genome. The influence of genes on metabolite levels, however, remains largely unknown, particularly for the many genes encoding non‐enzymatic proteins. Serendipitously, genomewide association studies explore the relationship between genetic variants and metabolite levels, but a comprehensive interaction network has remained elusive even for the simplest single‐celled organisms. Here, we systematically mapped the association between > 3,800 single‐gene deletions in the bacterium Escherichia coli and relative concentrations of > 7,000 intracellular metabolite ions. Beyond expected metabolic changes in the proximity to abolished enzyme activities, the association map reveals a largely unknown landscape of gene–metabolite interactions that are not represented in metabolic models. Therefore, the map provides a unique resource for assessing the genetic basis of metabolic changes and conversely hypothesizing metabolic consequences of genetic alterations. We illustrate this by predicting metabolism‐related functions of 72 so far not annotated genes and by identifying key genes mediating the cellular response to environmental perturbations. |
format | Online Article Text |
id | pubmed-5293155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52931552017-02-07 Genomewide landscape of gene–metabolome associations in Escherichia coli Fuhrer, Tobias Zampieri, Mattia Sévin, Daniel C Sauer, Uwe Zamboni, Nicola Mol Syst Biol Articles Metabolism is one of the best‐understood cellular processes whose network topology of enzymatic reactions is determined by an organism's genome. The influence of genes on metabolite levels, however, remains largely unknown, particularly for the many genes encoding non‐enzymatic proteins. Serendipitously, genomewide association studies explore the relationship between genetic variants and metabolite levels, but a comprehensive interaction network has remained elusive even for the simplest single‐celled organisms. Here, we systematically mapped the association between > 3,800 single‐gene deletions in the bacterium Escherichia coli and relative concentrations of > 7,000 intracellular metabolite ions. Beyond expected metabolic changes in the proximity to abolished enzyme activities, the association map reveals a largely unknown landscape of gene–metabolite interactions that are not represented in metabolic models. Therefore, the map provides a unique resource for assessing the genetic basis of metabolic changes and conversely hypothesizing metabolic consequences of genetic alterations. We illustrate this by predicting metabolism‐related functions of 72 so far not annotated genes and by identifying key genes mediating the cellular response to environmental perturbations. John Wiley and Sons Inc. 2017-01-16 /pmc/articles/PMC5293155/ /pubmed/28093455 http://dx.doi.org/10.15252/msb.20167150 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Fuhrer, Tobias Zampieri, Mattia Sévin, Daniel C Sauer, Uwe Zamboni, Nicola Genomewide landscape of gene–metabolome associations in Escherichia coli |
title | Genomewide landscape of gene–metabolome associations in Escherichia coli
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title_full | Genomewide landscape of gene–metabolome associations in Escherichia coli
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title_fullStr | Genomewide landscape of gene–metabolome associations in Escherichia coli
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title_full_unstemmed | Genomewide landscape of gene–metabolome associations in Escherichia coli
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title_short | Genomewide landscape of gene–metabolome associations in Escherichia coli
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title_sort | genomewide landscape of gene–metabolome associations in escherichia coli |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293155/ https://www.ncbi.nlm.nih.gov/pubmed/28093455 http://dx.doi.org/10.15252/msb.20167150 |
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