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A quantitative model of nucleosome dynamics
The expression, replication and repair of eukaryotic genomes require the fundamental organizing unit of chromatin, the nucleosome, to be unwrapped and disassembled. We have developed a quantitative model of nucleosome dynamics which provides a fundamental understanding of these DNA processes. We cal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201853/ https://www.ncbi.nlm.nih.gov/pubmed/21764779 http://dx.doi.org/10.1093/nar/gkr422 |
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author | Forties, Robert A. North, Justin A. Javaid, Sarah Tabbaa, Omar P. Fishel, Richard Poirier, Michael G. Bundschuh, Ralf |
author_facet | Forties, Robert A. North, Justin A. Javaid, Sarah Tabbaa, Omar P. Fishel, Richard Poirier, Michael G. Bundschuh, Ralf |
author_sort | Forties, Robert A. |
collection | PubMed |
description | The expression, replication and repair of eukaryotic genomes require the fundamental organizing unit of chromatin, the nucleosome, to be unwrapped and disassembled. We have developed a quantitative model of nucleosome dynamics which provides a fundamental understanding of these DNA processes. We calibrated this model using results from high precision single molecule nucleosome unzipping experiments, and then tested its predictions for experiments in which nucleosomes are disassembled by the DNA mismatch recognition complex hMSH2-hMSH6. We found that this calibrated model quantitatively describes hMSH2-hMSH6 induced disassembly rates of nucleosomes with two separate DNA sequences and four distinct histone modification states. In addition, this model provides mechanistic insight into nucleosome disassembly by hMSH2-hMSH6 and the influence of histone modifications on this disassembly reaction. This model's precise agreement with current experiments suggests that it can be applied more generally to provide important mechanistic understanding of the numerous nucleosome alterations that occur during DNA processing. |
format | Online Article Text |
id | pubmed-3201853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32018532011-10-26 A quantitative model of nucleosome dynamics Forties, Robert A. North, Justin A. Javaid, Sarah Tabbaa, Omar P. Fishel, Richard Poirier, Michael G. Bundschuh, Ralf Nucleic Acids Res Computational Biology The expression, replication and repair of eukaryotic genomes require the fundamental organizing unit of chromatin, the nucleosome, to be unwrapped and disassembled. We have developed a quantitative model of nucleosome dynamics which provides a fundamental understanding of these DNA processes. We calibrated this model using results from high precision single molecule nucleosome unzipping experiments, and then tested its predictions for experiments in which nucleosomes are disassembled by the DNA mismatch recognition complex hMSH2-hMSH6. We found that this calibrated model quantitatively describes hMSH2-hMSH6 induced disassembly rates of nucleosomes with two separate DNA sequences and four distinct histone modification states. In addition, this model provides mechanistic insight into nucleosome disassembly by hMSH2-hMSH6 and the influence of histone modifications on this disassembly reaction. This model's precise agreement with current experiments suggests that it can be applied more generally to provide important mechanistic understanding of the numerous nucleosome alterations that occur during DNA processing. Oxford University Press 2011-10 2011-07-15 /pmc/articles/PMC3201853/ /pubmed/21764779 http://dx.doi.org/10.1093/nar/gkr422 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Forties, Robert A. North, Justin A. Javaid, Sarah Tabbaa, Omar P. Fishel, Richard Poirier, Michael G. Bundschuh, Ralf A quantitative model of nucleosome dynamics |
title | A quantitative model of nucleosome dynamics |
title_full | A quantitative model of nucleosome dynamics |
title_fullStr | A quantitative model of nucleosome dynamics |
title_full_unstemmed | A quantitative model of nucleosome dynamics |
title_short | A quantitative model of nucleosome dynamics |
title_sort | quantitative model of nucleosome dynamics |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201853/ https://www.ncbi.nlm.nih.gov/pubmed/21764779 http://dx.doi.org/10.1093/nar/gkr422 |
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