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Mechanistic stochastic model of histone modification pattern formation
BACKGROUND: The activity of a single gene is influenced by the composition of the chromatin in which it is embedded. Nucleosome turnover, conformational dynamics, and covalent histone modifications each induce changes in the structure of chromatin and its affinity for regulatory proteins. The dynami...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234852/ https://www.ncbi.nlm.nih.gov/pubmed/25408711 http://dx.doi.org/10.1186/1756-8935-7-30 |
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author | Anink-Groenen, Lisette C M Maarleveld, Timo R Verschure, Pernette J Bruggeman, Frank J |
author_facet | Anink-Groenen, Lisette C M Maarleveld, Timo R Verschure, Pernette J Bruggeman, Frank J |
author_sort | Anink-Groenen, Lisette C M |
collection | PubMed |
description | BACKGROUND: The activity of a single gene is influenced by the composition of the chromatin in which it is embedded. Nucleosome turnover, conformational dynamics, and covalent histone modifications each induce changes in the structure of chromatin and its affinity for regulatory proteins. The dynamics of histone modifications and the persistence of modification patterns for long periods are still largely unknown. RESULTS: In this study, we present a stochastic mathematical model that describes the molecular mechanisms of histone modification pattern formation along a single gene, with non-phenomenological, physical parameters. We find that diffusion and recruitment properties of histone modifying enzymes together with chromatin connectivity allow for a rich repertoire of stochastic histone modification dynamics and pattern formation. We demonstrate that histone modification patterns at a single gene can be established or removed within a few minutes through diffusion and weak recruitment mechanisms of histone modification spreading. Moreover, we show that strong synergism between diffusion and weak recruitment mechanisms leads to nearly irreversible transitions in histone modification patterns providing stable patterns. In the absence of chromatin connectivity spontaneous and dynamic histone modification boundaries can be formed that are highly unstable, and spontaneous fluctuations cause them to diffuse randomly. Chromatin connectivity destabilizes this synergistic system and introduces bistability, illustrating state switching between opposing modification states of the model gene. The observed bistable long-range and localized pattern formation are critical effectors of gene expression regulation. CONCLUSION: This study illustrates how the cooperative interactions between regulatory proteins and the chromatin state generate complex stochastic dynamics of gene expression regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1756-8935-7-30) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4234852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42348522014-11-19 Mechanistic stochastic model of histone modification pattern formation Anink-Groenen, Lisette C M Maarleveld, Timo R Verschure, Pernette J Bruggeman, Frank J Epigenetics Chromatin Research BACKGROUND: The activity of a single gene is influenced by the composition of the chromatin in which it is embedded. Nucleosome turnover, conformational dynamics, and covalent histone modifications each induce changes in the structure of chromatin and its affinity for regulatory proteins. The dynamics of histone modifications and the persistence of modification patterns for long periods are still largely unknown. RESULTS: In this study, we present a stochastic mathematical model that describes the molecular mechanisms of histone modification pattern formation along a single gene, with non-phenomenological, physical parameters. We find that diffusion and recruitment properties of histone modifying enzymes together with chromatin connectivity allow for a rich repertoire of stochastic histone modification dynamics and pattern formation. We demonstrate that histone modification patterns at a single gene can be established or removed within a few minutes through diffusion and weak recruitment mechanisms of histone modification spreading. Moreover, we show that strong synergism between diffusion and weak recruitment mechanisms leads to nearly irreversible transitions in histone modification patterns providing stable patterns. In the absence of chromatin connectivity spontaneous and dynamic histone modification boundaries can be formed that are highly unstable, and spontaneous fluctuations cause them to diffuse randomly. Chromatin connectivity destabilizes this synergistic system and introduces bistability, illustrating state switching between opposing modification states of the model gene. The observed bistable long-range and localized pattern formation are critical effectors of gene expression regulation. CONCLUSION: This study illustrates how the cooperative interactions between regulatory proteins and the chromatin state generate complex stochastic dynamics of gene expression regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1756-8935-7-30) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-27 /pmc/articles/PMC4234852/ /pubmed/25408711 http://dx.doi.org/10.1186/1756-8935-7-30 Text en © Anink-Groenen et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Anink-Groenen, Lisette C M Maarleveld, Timo R Verschure, Pernette J Bruggeman, Frank J Mechanistic stochastic model of histone modification pattern formation |
title | Mechanistic stochastic model of histone modification pattern formation |
title_full | Mechanistic stochastic model of histone modification pattern formation |
title_fullStr | Mechanistic stochastic model of histone modification pattern formation |
title_full_unstemmed | Mechanistic stochastic model of histone modification pattern formation |
title_short | Mechanistic stochastic model of histone modification pattern formation |
title_sort | mechanistic stochastic model of histone modification pattern formation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234852/ https://www.ncbi.nlm.nih.gov/pubmed/25408711 http://dx.doi.org/10.1186/1756-8935-7-30 |
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