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A simple biophysical model emulates budding yeast chromosome condensation

Mitotic chromosomes were one of the first cell biological structures to be described, yet their molecular architecture remains poorly understood. We have devised a simple biophysical model of a 300 kb-long nucleosome chain, the size of a budding yeast chromosome, constrained by interactions between...

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Autores principales: Cheng, Tammy MK, Heeger, Sebastian, Chaleil, Raphaël AG, Matthews, Nik, Stewart, Aengus, Wright, Jon, Lim, Carmay, Bates, Paul A, Uhlmann, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413874/
https://www.ncbi.nlm.nih.gov/pubmed/25922992
http://dx.doi.org/10.7554/eLife.05565
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author Cheng, Tammy MK
Heeger, Sebastian
Chaleil, Raphaël AG
Matthews, Nik
Stewart, Aengus
Wright, Jon
Lim, Carmay
Bates, Paul A
Uhlmann, Frank
author_facet Cheng, Tammy MK
Heeger, Sebastian
Chaleil, Raphaël AG
Matthews, Nik
Stewart, Aengus
Wright, Jon
Lim, Carmay
Bates, Paul A
Uhlmann, Frank
author_sort Cheng, Tammy MK
collection PubMed
description Mitotic chromosomes were one of the first cell biological structures to be described, yet their molecular architecture remains poorly understood. We have devised a simple biophysical model of a 300 kb-long nucleosome chain, the size of a budding yeast chromosome, constrained by interactions between binding sites of the chromosomal condensin complex, a key component of interphase and mitotic chromosomes. Comparisons of computational and experimental (4C) interaction maps, and other biophysical features, allow us to predict a mode of condensin action. Stochastic condensin-mediated pairwise interactions along the nucleosome chain generate native-like chromosome features and recapitulate chromosome compaction and individualization during mitotic condensation. Higher order interactions between condensin binding sites explain the data less well. Our results suggest that basic assumptions about chromatin behavior go a long way to explain chromosome architecture and are able to generate a molecular model of what the inside of a chromosome is likely to look like. DOI: http://dx.doi.org/10.7554/eLife.05565.001
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spelling pubmed-44138742015-05-01 A simple biophysical model emulates budding yeast chromosome condensation Cheng, Tammy MK Heeger, Sebastian Chaleil, Raphaël AG Matthews, Nik Stewart, Aengus Wright, Jon Lim, Carmay Bates, Paul A Uhlmann, Frank eLife Computational and Systems Biology Mitotic chromosomes were one of the first cell biological structures to be described, yet their molecular architecture remains poorly understood. We have devised a simple biophysical model of a 300 kb-long nucleosome chain, the size of a budding yeast chromosome, constrained by interactions between binding sites of the chromosomal condensin complex, a key component of interphase and mitotic chromosomes. Comparisons of computational and experimental (4C) interaction maps, and other biophysical features, allow us to predict a mode of condensin action. Stochastic condensin-mediated pairwise interactions along the nucleosome chain generate native-like chromosome features and recapitulate chromosome compaction and individualization during mitotic condensation. Higher order interactions between condensin binding sites explain the data less well. Our results suggest that basic assumptions about chromatin behavior go a long way to explain chromosome architecture and are able to generate a molecular model of what the inside of a chromosome is likely to look like. DOI: http://dx.doi.org/10.7554/eLife.05565.001 eLife Sciences Publications, Ltd 2015-04-29 /pmc/articles/PMC4413874/ /pubmed/25922992 http://dx.doi.org/10.7554/eLife.05565 Text en © 2015, Cheng et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Cheng, Tammy MK
Heeger, Sebastian
Chaleil, Raphaël AG
Matthews, Nik
Stewart, Aengus
Wright, Jon
Lim, Carmay
Bates, Paul A
Uhlmann, Frank
A simple biophysical model emulates budding yeast chromosome condensation
title A simple biophysical model emulates budding yeast chromosome condensation
title_full A simple biophysical model emulates budding yeast chromosome condensation
title_fullStr A simple biophysical model emulates budding yeast chromosome condensation
title_full_unstemmed A simple biophysical model emulates budding yeast chromosome condensation
title_short A simple biophysical model emulates budding yeast chromosome condensation
title_sort simple biophysical model emulates budding yeast chromosome condensation
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413874/
https://www.ncbi.nlm.nih.gov/pubmed/25922992
http://dx.doi.org/10.7554/eLife.05565
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