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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Main Authors: Joana C Xavier, Kiran Raosaheb Patil, Isabel Rocha
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-11-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1006556
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spelling doaj-51b14f8e24754770a9bc13e53740998a2021-04-21T15:12:36ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582018-11-011411e100655610.1371/journal.pcbi.1006556Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes.Joana C XavierKiran Raosaheb PatilIsabel RochaEssential 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.https://doi.org/10.1371/journal.pcbi.1006556
collection DOAJ
language English
format Article
sources DOAJ
author Joana C Xavier
Kiran Raosaheb Patil
Isabel Rocha
spellingShingle Joana C Xavier
Kiran Raosaheb Patil
Isabel Rocha
Metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes.
PLoS Computational Biology
author_facet Joana C Xavier
Kiran Raosaheb Patil
Isabel Rocha
author_sort Joana C Xavier
title 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_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_sort metabolic models and gene essentiality data reveal essential and conserved metabolism in prokaryotes.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2018-11-01
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.
url https://doi.org/10.1371/journal.pcbi.1006556
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