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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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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. |
format | Online Article Text |
id | pubmed-5294885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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