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Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes
Using molecular dynamics simulations, we show here that growing plectonemes resulting from transcription-induced supercoiling have the ability to actively push cohesin rings along chromatin fibres. The pushing direction is such that within each topologically associating domain (TAD) cohesin rings fo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829651/ https://www.ncbi.nlm.nih.gov/pubmed/29140466 http://dx.doi.org/10.1093/nar/gkx1123 |
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author | Racko, Dusan Benedetti, Fabrizio Dorier, Julien Stasiak, Andrzej |
author_facet | Racko, Dusan Benedetti, Fabrizio Dorier, Julien Stasiak, Andrzej |
author_sort | Racko, Dusan |
collection | PubMed |
description | Using molecular dynamics simulations, we show here that growing plectonemes resulting from transcription-induced supercoiling have the ability to actively push cohesin rings along chromatin fibres. The pushing direction is such that within each topologically associating domain (TAD) cohesin rings forming handcuffs move from the source of supercoiling, constituted by RNA polymerase with associated DNA topoisomerase TOP1, towards borders of TADs, where supercoiling is released by topoisomerase TOPIIB. Cohesin handcuffs are pushed by continuous flux of supercoiling that is generated by transcription and is then progressively released by action of TOPIIB located at TADs borders. Our model explains what can be the driving force of chromatin loop extrusion and how it can be ensured that loops grow quickly and in a good direction. In addition, the supercoiling-driven loop extrusion mechanism is consistent with earlier explanations proposing why TADs flanked by convergent CTCF binding sites form more stable chromatin loops than TADs flanked by divergent CTCF binding sites. We discuss the role of supercoiling in stimulating enhancer promoter contacts and propose that transcription of eRNA sends the first wave of supercoiling that can activate mRNA transcription in a given TAD. |
format | Online Article Text |
id | pubmed-5829651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58296512018-03-06 Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes Racko, Dusan Benedetti, Fabrizio Dorier, Julien Stasiak, Andrzej Nucleic Acids Res Computational Biology Using molecular dynamics simulations, we show here that growing plectonemes resulting from transcription-induced supercoiling have the ability to actively push cohesin rings along chromatin fibres. The pushing direction is such that within each topologically associating domain (TAD) cohesin rings forming handcuffs move from the source of supercoiling, constituted by RNA polymerase with associated DNA topoisomerase TOP1, towards borders of TADs, where supercoiling is released by topoisomerase TOPIIB. Cohesin handcuffs are pushed by continuous flux of supercoiling that is generated by transcription and is then progressively released by action of TOPIIB located at TADs borders. Our model explains what can be the driving force of chromatin loop extrusion and how it can be ensured that loops grow quickly and in a good direction. In addition, the supercoiling-driven loop extrusion mechanism is consistent with earlier explanations proposing why TADs flanked by convergent CTCF binding sites form more stable chromatin loops than TADs flanked by divergent CTCF binding sites. We discuss the role of supercoiling in stimulating enhancer promoter contacts and propose that transcription of eRNA sends the first wave of supercoiling that can activate mRNA transcription in a given TAD. Oxford University Press 2018-02-28 2017-11-13 /pmc/articles/PMC5829651/ /pubmed/29140466 http://dx.doi.org/10.1093/nar/gkx1123 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Racko, Dusan Benedetti, Fabrizio Dorier, Julien Stasiak, Andrzej Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title | Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title_full | Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title_fullStr | Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title_full_unstemmed | Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title_short | Transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of TADs in interphase chromosomes |
title_sort | transcription-induced supercoiling as the driving force of chromatin loop extrusion during formation of tads in interphase chromosomes |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829651/ https://www.ncbi.nlm.nih.gov/pubmed/29140466 http://dx.doi.org/10.1093/nar/gkx1123 |
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