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Understanding Metabolic Flux Behaviour in Whole-Cell Model Output
Whole-cell modelling is a newly expanding field that has many applications in lab experiment design and predictive drug testing. Although whole-cell model output contains a wealth of information, it is complex and high dimensional and thus hard to interpret. Here, we present an analysis pipeline tha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718694/ https://www.ncbi.nlm.nih.gov/pubmed/34977150 http://dx.doi.org/10.3389/fmolb.2021.732079 |
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author | Landon, Sophie Chalkley, Oliver Breese, Gus Grierson, Claire Marucci, Lucia |
author_facet | Landon, Sophie Chalkley, Oliver Breese, Gus Grierson, Claire Marucci, Lucia |
author_sort | Landon, Sophie |
collection | PubMed |
description | Whole-cell modelling is a newly expanding field that has many applications in lab experiment design and predictive drug testing. Although whole-cell model output contains a wealth of information, it is complex and high dimensional and thus hard to interpret. Here, we present an analysis pipeline that combines machine learning, dimensionality reduction, and network analysis to interpret and visualise metabolic reaction fluxes from a set of single gene knockouts simulated in the Mycoplasma genitalium whole-cell model. We found that the reaction behaviours show trends that correlate with phenotypic classes of the simulation output, highlighting particular cellular subsystems that malfunction after gene knockouts. From a graphical representation of the metabolic network, we saw that there is a set of reactions that can be used as markers of a phenotypic class, showing their importance within the network. Our analysis pipeline can support the understanding of the complexity of in silico cells without detailed knowledge of the constituent parts, which can help to understand the effects of gene knockouts and, as whole-cell models become more widely built and used, aid genome design. |
format | Online Article Text |
id | pubmed-8718694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87186942022-01-01 Understanding Metabolic Flux Behaviour in Whole-Cell Model Output Landon, Sophie Chalkley, Oliver Breese, Gus Grierson, Claire Marucci, Lucia Front Mol Biosci Molecular Biosciences Whole-cell modelling is a newly expanding field that has many applications in lab experiment design and predictive drug testing. Although whole-cell model output contains a wealth of information, it is complex and high dimensional and thus hard to interpret. Here, we present an analysis pipeline that combines machine learning, dimensionality reduction, and network analysis to interpret and visualise metabolic reaction fluxes from a set of single gene knockouts simulated in the Mycoplasma genitalium whole-cell model. We found that the reaction behaviours show trends that correlate with phenotypic classes of the simulation output, highlighting particular cellular subsystems that malfunction after gene knockouts. From a graphical representation of the metabolic network, we saw that there is a set of reactions that can be used as markers of a phenotypic class, showing their importance within the network. Our analysis pipeline can support the understanding of the complexity of in silico cells without detailed knowledge of the constituent parts, which can help to understand the effects of gene knockouts and, as whole-cell models become more widely built and used, aid genome design. Frontiers Media S.A. 2021-12-17 /pmc/articles/PMC8718694/ /pubmed/34977150 http://dx.doi.org/10.3389/fmolb.2021.732079 Text en Copyright © 2021 Landon, Chalkley, Breese, Grierson and Marucci. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Landon, Sophie Chalkley, Oliver Breese, Gus Grierson, Claire Marucci, Lucia Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title | Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title_full | Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title_fullStr | Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title_full_unstemmed | Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title_short | Understanding Metabolic Flux Behaviour in Whole-Cell Model Output |
title_sort | understanding metabolic flux behaviour in whole-cell model output |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718694/ https://www.ncbi.nlm.nih.gov/pubmed/34977150 http://dx.doi.org/10.3389/fmolb.2021.732079 |
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