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Exact quantification of cellular robustness in genome-scale metabolic networks

Motivation: Robustness, the ability of biological networks to uphold their functionality in spite of perturbations, is a key characteristic of all living systems. Although several theoretical approaches have been developed to formalize robustness, it still eludes an exact quantification. Here, we pr...

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Autores principales: Gerstl, Matthias P., Klamt, Steffen, Jungreuthmayer, Christian, Zanghellini, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795620/
https://www.ncbi.nlm.nih.gov/pubmed/26543173
http://dx.doi.org/10.1093/bioinformatics/btv649
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author Gerstl, Matthias P.
Klamt, Steffen
Jungreuthmayer, Christian
Zanghellini, Jürgen
author_facet Gerstl, Matthias P.
Klamt, Steffen
Jungreuthmayer, Christian
Zanghellini, Jürgen
author_sort Gerstl, Matthias P.
collection PubMed
description Motivation: Robustness, the ability of biological networks to uphold their functionality in spite of perturbations, is a key characteristic of all living systems. Although several theoretical approaches have been developed to formalize robustness, it still eludes an exact quantification. Here, we present a rigorous and quantitative approach for the structural robustness of metabolic networks by measuring their ability to tolerate random reaction (or gene) knockouts. Results: In analogy to reliability theory, based on an explicit consideration of all possible knockout sets, we exactly quantify the probability of failure for a given network function (e.g. growth). This measure can be computed if the network’s minimal cut sets (MSCs) are known. We show that even in genome-scale metabolic networks the probability of (network) failure can be reliably estimated from MSCs with lowest cardinalities. We demonstrate the applicability of our theory by analyzing the structural robustness of multiple Enterobacteriaceae and Blattibacteriaceae and show a dramatically low structural robustness for the latter. We find that structural robustness develops from the ability to proliferate in multiple growth environments consistent with experimentally found knowledge. Conclusion: The probability of (network) failure provides thus a reliable and easily computable measure of structural robustness and redundancy in (genome-scale) metabolic networks. Availability and implementation: Source code is available under the GNU General Public License at https://github.com/mpgerstl/networkRobustnessToolbox. Contact: juergen.zanghellini@boku.ac.at Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-47956202016-03-21 Exact quantification of cellular robustness in genome-scale metabolic networks Gerstl, Matthias P. Klamt, Steffen Jungreuthmayer, Christian Zanghellini, Jürgen Bioinformatics Original Papers Motivation: Robustness, the ability of biological networks to uphold their functionality in spite of perturbations, is a key characteristic of all living systems. Although several theoretical approaches have been developed to formalize robustness, it still eludes an exact quantification. Here, we present a rigorous and quantitative approach for the structural robustness of metabolic networks by measuring their ability to tolerate random reaction (or gene) knockouts. Results: In analogy to reliability theory, based on an explicit consideration of all possible knockout sets, we exactly quantify the probability of failure for a given network function (e.g. growth). This measure can be computed if the network’s minimal cut sets (MSCs) are known. We show that even in genome-scale metabolic networks the probability of (network) failure can be reliably estimated from MSCs with lowest cardinalities. We demonstrate the applicability of our theory by analyzing the structural robustness of multiple Enterobacteriaceae and Blattibacteriaceae and show a dramatically low structural robustness for the latter. We find that structural robustness develops from the ability to proliferate in multiple growth environments consistent with experimentally found knowledge. Conclusion: The probability of (network) failure provides thus a reliable and easily computable measure of structural robustness and redundancy in (genome-scale) metabolic networks. Availability and implementation: Source code is available under the GNU General Public License at https://github.com/mpgerstl/networkRobustnessToolbox. Contact: juergen.zanghellini@boku.ac.at Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2016-03-01 2015-11-04 /pmc/articles/PMC4795620/ /pubmed/26543173 http://dx.doi.org/10.1093/bioinformatics/btv649 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Papers
Gerstl, Matthias P.
Klamt, Steffen
Jungreuthmayer, Christian
Zanghellini, Jürgen
Exact quantification of cellular robustness in genome-scale metabolic networks
title Exact quantification of cellular robustness in genome-scale metabolic networks
title_full Exact quantification of cellular robustness in genome-scale metabolic networks
title_fullStr Exact quantification of cellular robustness in genome-scale metabolic networks
title_full_unstemmed Exact quantification of cellular robustness in genome-scale metabolic networks
title_short Exact quantification of cellular robustness in genome-scale metabolic networks
title_sort exact quantification of cellular robustness in genome-scale metabolic networks
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795620/
https://www.ncbi.nlm.nih.gov/pubmed/26543173
http://dx.doi.org/10.1093/bioinformatics/btv649
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