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Markov State Models of gene regulatory networks

BACKGROUND: Gene regulatory networks with dynamics characterized by multiple stable states underlie cell fate-decisions. Quantitative models that can link molecular-level knowledge of gene regulation to a global understanding of network dynamics have the potential to guide cell-reprogramming strateg...

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Autores principales: Chu, Brian K., Tse, Margaret J., Sato, Royce R., Read, Elizabeth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294885/
https://www.ncbi.nlm.nih.gov/pubmed/28166778
http://dx.doi.org/10.1186/s12918-017-0394-4
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author Chu, Brian K.
Tse, Margaret J.
Sato, Royce R.
Read, Elizabeth L.
author_facet Chu, Brian K.
Tse, Margaret J.
Sato, Royce R.
Read, Elizabeth L.
author_sort Chu, Brian K.
collection PubMed
description BACKGROUND: Gene regulatory networks with dynamics characterized by multiple stable states underlie cell fate-decisions. Quantitative models that can link molecular-level knowledge of gene regulation to a global understanding of network dynamics have the potential to guide cell-reprogramming strategies. Networks are often modeled by the stochastic Chemical Master Equation, but methods for systematic identification of key properties of the global dynamics are currently lacking. RESULTS: The method identifies the number, phenotypes, and lifetimes of long-lived states for a set of common gene regulatory network models. Application of transition path theory to the constructed Markov State Model decomposes global dynamics into a set of dominant transition paths and associated relative probabilities for stochastic state-switching. CONCLUSIONS: In this proof-of-concept study, we found that the Markov State Model provides a general framework for analyzing and visualizing stochastic multistability and state-transitions in gene networks. Our results suggest that this framework—adopted from the field of atomistic Molecular Dynamics—can be a useful tool for quantitative Systems Biology at the network scale. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0394-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-52948852017-02-09 Markov State Models of gene regulatory networks Chu, Brian K. Tse, Margaret J. Sato, Royce R. Read, Elizabeth L. BMC Syst Biol Research Article BACKGROUND: Gene regulatory networks with dynamics characterized by multiple stable states underlie cell fate-decisions. Quantitative models that can link molecular-level knowledge of gene regulation to a global understanding of network dynamics have the potential to guide cell-reprogramming strategies. Networks are often modeled by the stochastic Chemical Master Equation, but methods for systematic identification of key properties of the global dynamics are currently lacking. RESULTS: The method identifies the number, phenotypes, and lifetimes of long-lived states for a set of common gene regulatory network models. Application of transition path theory to the constructed Markov State Model decomposes global dynamics into a set of dominant transition paths and associated relative probabilities for stochastic state-switching. CONCLUSIONS: In this proof-of-concept study, we found that the Markov State Model provides a general framework for analyzing and visualizing stochastic multistability and state-transitions in gene networks. Our results suggest that this framework—adopted from the field of atomistic Molecular Dynamics—can be a useful tool for quantitative Systems Biology at the network scale. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0394-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-06 /pmc/articles/PMC5294885/ /pubmed/28166778 http://dx.doi.org/10.1186/s12918-017-0394-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chu, Brian K.
Tse, Margaret J.
Sato, Royce R.
Read, Elizabeth L.
Markov State Models of gene regulatory networks
title Markov State Models of gene regulatory networks
title_full Markov State Models of gene regulatory networks
title_fullStr Markov State Models of gene regulatory networks
title_full_unstemmed Markov State Models of gene regulatory networks
title_short Markov State Models of gene regulatory networks
title_sort markov state models of gene regulatory networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294885/
https://www.ncbi.nlm.nih.gov/pubmed/28166778
http://dx.doi.org/10.1186/s12918-017-0394-4
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