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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Online Access: | https://doi.org/10.1371/journal.pcbi.1006556 |
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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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