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The Rabl configuration limits topological entanglement of chromosomes in budding yeast
The three dimensional organization of genomes remains mostly unknown due to their high degree of condensation. Biophysical studies predict that condensation promotes the topological entanglement of chromatin fibers and the inhibition of function. How organisms balance between functionally active gen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494875/ https://www.ncbi.nlm.nih.gov/pubmed/31043625 http://dx.doi.org/10.1038/s41598-019-42967-4 |
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author | Pouokam, Maxime Cruz, Brian Burgess, Sean Segal, Mark R. Vazquez, Mariel Arsuaga, Javier |
author_facet | Pouokam, Maxime Cruz, Brian Burgess, Sean Segal, Mark R. Vazquez, Mariel Arsuaga, Javier |
author_sort | Pouokam, Maxime |
collection | PubMed |
description | The three dimensional organization of genomes remains mostly unknown due to their high degree of condensation. Biophysical studies predict that condensation promotes the topological entanglement of chromatin fibers and the inhibition of function. How organisms balance between functionally active genomes and a high degree of condensation remains to be determined. Here we hypothesize that the Rabl configuration, characterized by the attachment of centromeres and telomeres to the nuclear envelope, helps to reduce the topological entanglement of chromosomes. To test this hypothesis we developed a novel method to quantify chromosome entanglement complexity in 3D reconstructions obtained from Chromosome Conformation Capture (CCC) data. Applying this method to published data of the yeast genome, we show that computational models implementing the attachment of telomeres or centromeres alone are not sufficient to obtain the reduced entanglement complexity observed in 3D reconstructions. It is only when the centromeres and telomeres are attached to the nuclear envelope (i.e. the Rabl configuration) that the complexity of entanglement of the genome is comparable to that of the 3D reconstructions. We therefore suggest that the Rabl configuration is an essential player in the simplification of the entanglement of chromatin fibers. |
format | Online Article Text |
id | pubmed-6494875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64948752019-05-17 The Rabl configuration limits topological entanglement of chromosomes in budding yeast Pouokam, Maxime Cruz, Brian Burgess, Sean Segal, Mark R. Vazquez, Mariel Arsuaga, Javier Sci Rep Article The three dimensional organization of genomes remains mostly unknown due to their high degree of condensation. Biophysical studies predict that condensation promotes the topological entanglement of chromatin fibers and the inhibition of function. How organisms balance between functionally active genomes and a high degree of condensation remains to be determined. Here we hypothesize that the Rabl configuration, characterized by the attachment of centromeres and telomeres to the nuclear envelope, helps to reduce the topological entanglement of chromosomes. To test this hypothesis we developed a novel method to quantify chromosome entanglement complexity in 3D reconstructions obtained from Chromosome Conformation Capture (CCC) data. Applying this method to published data of the yeast genome, we show that computational models implementing the attachment of telomeres or centromeres alone are not sufficient to obtain the reduced entanglement complexity observed in 3D reconstructions. It is only when the centromeres and telomeres are attached to the nuclear envelope (i.e. the Rabl configuration) that the complexity of entanglement of the genome is comparable to that of the 3D reconstructions. We therefore suggest that the Rabl configuration is an essential player in the simplification of the entanglement of chromatin fibers. Nature Publishing Group UK 2019-05-01 /pmc/articles/PMC6494875/ /pubmed/31043625 http://dx.doi.org/10.1038/s41598-019-42967-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Pouokam, Maxime Cruz, Brian Burgess, Sean Segal, Mark R. Vazquez, Mariel Arsuaga, Javier The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title_full | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title_fullStr | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title_full_unstemmed | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title_short | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
title_sort | rabl configuration limits topological entanglement of chromosomes in budding yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494875/ https://www.ncbi.nlm.nih.gov/pubmed/31043625 http://dx.doi.org/10.1038/s41598-019-42967-4 |
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