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Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining
Sister chromatid intertwines (SCIs), or catenanes, are topological links between replicated chromatids that interfere with chromosome segregation. The formation of SCIs is thought to be a consequence of fork swiveling during DNA replication, and their removal is thought to occur because of the intri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065527/ https://www.ncbi.nlm.nih.gov/pubmed/27716481 http://dx.doi.org/10.1016/j.molcel.2016.09.007 |
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author | Sen, Nicholas Leonard, Joanne Torres, Raul Garcia-Luis, Jonay Palou-Marin, Gloria Aragón, Luis |
author_facet | Sen, Nicholas Leonard, Joanne Torres, Raul Garcia-Luis, Jonay Palou-Marin, Gloria Aragón, Luis |
author_sort | Sen, Nicholas |
collection | PubMed |
description | Sister chromatid intertwines (SCIs), or catenanes, are topological links between replicated chromatids that interfere with chromosome segregation. The formation of SCIs is thought to be a consequence of fork swiveling during DNA replication, and their removal is thought to occur because of the intrinsic feature of type II topoisomerases (Top2) to simplify DNA topology. Here, we report that SCIs are also formed independently of DNA replication during G(2)/M by Top2-dependent concatenation of cohesed chromatids due to their physical proximity. We demonstrate that, in contrast to G(2)/M, Top2 removes SCIs from cohesed chromatids at the anaphase onset. Importantly, SCI removal in anaphase requires condensin and coincides with the hyperactivation of condensin DNA supercoiling activity. This is consistent with the longstanding proposal that condensin provides a bias in Top2 function toward decatenation. A comprehensive model for the formation and resolution of toxic SCI entanglements on eukaryotic genomes is proposed. |
format | Online Article Text |
id | pubmed-5065527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50655272016-10-20 Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining Sen, Nicholas Leonard, Joanne Torres, Raul Garcia-Luis, Jonay Palou-Marin, Gloria Aragón, Luis Mol Cell Article Sister chromatid intertwines (SCIs), or catenanes, are topological links between replicated chromatids that interfere with chromosome segregation. The formation of SCIs is thought to be a consequence of fork swiveling during DNA replication, and their removal is thought to occur because of the intrinsic feature of type II topoisomerases (Top2) to simplify DNA topology. Here, we report that SCIs are also formed independently of DNA replication during G(2)/M by Top2-dependent concatenation of cohesed chromatids due to their physical proximity. We demonstrate that, in contrast to G(2)/M, Top2 removes SCIs from cohesed chromatids at the anaphase onset. Importantly, SCI removal in anaphase requires condensin and coincides with the hyperactivation of condensin DNA supercoiling activity. This is consistent with the longstanding proposal that condensin provides a bias in Top2 function toward decatenation. A comprehensive model for the formation and resolution of toxic SCI entanglements on eukaryotic genomes is proposed. Cell Press 2016-10-06 /pmc/articles/PMC5065527/ /pubmed/27716481 http://dx.doi.org/10.1016/j.molcel.2016.09.007 Text en Crown Copyright © 2016 Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sen, Nicholas Leonard, Joanne Torres, Raul Garcia-Luis, Jonay Palou-Marin, Gloria Aragón, Luis Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title | Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title_full | Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title_fullStr | Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title_full_unstemmed | Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title_short | Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining |
title_sort | physical proximity of sister chromatids promotes top2-dependent intertwining |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065527/ https://www.ncbi.nlm.nih.gov/pubmed/27716481 http://dx.doi.org/10.1016/j.molcel.2016.09.007 |
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