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Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes

Essential metabolic reactions are shaping constituents of metabolic networks, enabling viable and distinct phenotypes across diverse life forms. Here we analyse and compare modelling predictions of essential metabolic functions with experimental data and thereby identify core metabolic pathways in p...

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Autores principales: Xavier, Joana C., Patil, Kiran Raosaheb, Rocha, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283598/
https://www.ncbi.nlm.nih.gov/pubmed/30444863
http://dx.doi.org/10.1371/journal.pcbi.1006556
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author Xavier, Joana C.
Patil, Kiran Raosaheb
Rocha, Isabel
author_facet Xavier, Joana C.
Patil, Kiran Raosaheb
Rocha, Isabel
author_sort Xavier, Joana C.
collection PubMed
description Essential metabolic reactions are shaping constituents of metabolic networks, enabling viable and distinct phenotypes across diverse life forms. Here we analyse and compare modelling predictions of essential metabolic functions with experimental data and thereby identify core metabolic pathways in prokaryotes. Simulations of 15 manually curated genome-scale metabolic models were integrated with 36 large-scale gene essentiality datasets encompassing a wide variety of species of bacteria and archaea. Conservation of metabolic genes was estimated by analysing 79 representative genomes from all the branches of the prokaryotic tree of life. We find that essentiality patterns reflect phylogenetic relations both for modelling and experimental data, which correlate highly at the pathway level. Genes that are essential for several species tend to be highly conserved as opposed to non-essential genes which may be conserved or not. The tRNA-charging module is highlighted as ancestral and with high centrality in the networks, followed closely by cofactor metabolism, pointing to an early information processing system supplied by organic cofactors. The results, which point to model improvements and also indicate faults in the experimental data, should be relevant to the study of centrality in metabolic networks and ancient metabolism but also to metabolic engineering with prokaryotes.
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spelling pubmed-62835982018-12-19 Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes Xavier, Joana C. Patil, Kiran Raosaheb Rocha, Isabel PLoS Comput Biol Research Article Essential metabolic reactions are shaping constituents of metabolic networks, enabling viable and distinct phenotypes across diverse life forms. Here we analyse and compare modelling predictions of essential metabolic functions with experimental data and thereby identify core metabolic pathways in prokaryotes. Simulations of 15 manually curated genome-scale metabolic models were integrated with 36 large-scale gene essentiality datasets encompassing a wide variety of species of bacteria and archaea. Conservation of metabolic genes was estimated by analysing 79 representative genomes from all the branches of the prokaryotic tree of life. We find that essentiality patterns reflect phylogenetic relations both for modelling and experimental data, which correlate highly at the pathway level. Genes that are essential for several species tend to be highly conserved as opposed to non-essential genes which may be conserved or not. The tRNA-charging module is highlighted as ancestral and with high centrality in the networks, followed closely by cofactor metabolism, pointing to an early information processing system supplied by organic cofactors. The results, which point to model improvements and also indicate faults in the experimental data, should be relevant to the study of centrality in metabolic networks and ancient metabolism but also to metabolic engineering with prokaryotes. Public Library of Science 2018-11-16 /pmc/articles/PMC6283598/ /pubmed/30444863 http://dx.doi.org/10.1371/journal.pcbi.1006556 Text en © 2018 Xavier 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
Xavier, Joana C.
Patil, Kiran Raosaheb
Rocha, Isabel
Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title_full Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title_fullStr Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title_full_unstemmed Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title_short Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
title_sort metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283598/
https://www.ncbi.nlm.nih.gov/pubmed/30444863
http://dx.doi.org/10.1371/journal.pcbi.1006556
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