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Cohesin and CTCF control the dynamics of chromosome folding

In mammals, interactions between sequences within topologically associating domains enable control of gene expression across large genomic distances. Yet it is unknown how frequently such contacts occur, how long they last and how they depend on the dynamics of chromosome folding and loop extrusion...

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Autores principales: Mach, Pia, Kos, Pavel I., Zhan, Yinxiu, Cramard, Julie, Gaudin, Simon, Tünnermann, Jana, Marchi, Edoardo, Eglinger, Jan, Zuin, Jessica, Kryzhanovska, Mariya, Smallwood, Sebastien, Gelman, Laurent, Roth, Gregory, Nora, Elphège P., Tiana, Guido, Giorgetti, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729113/
https://www.ncbi.nlm.nih.gov/pubmed/36471076
http://dx.doi.org/10.1038/s41588-022-01232-7
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author Mach, Pia
Kos, Pavel I.
Zhan, Yinxiu
Cramard, Julie
Gaudin, Simon
Tünnermann, Jana
Marchi, Edoardo
Eglinger, Jan
Zuin, Jessica
Kryzhanovska, Mariya
Smallwood, Sebastien
Gelman, Laurent
Roth, Gregory
Nora, Elphège P.
Tiana, Guido
Giorgetti, Luca
author_facet Mach, Pia
Kos, Pavel I.
Zhan, Yinxiu
Cramard, Julie
Gaudin, Simon
Tünnermann, Jana
Marchi, Edoardo
Eglinger, Jan
Zuin, Jessica
Kryzhanovska, Mariya
Smallwood, Sebastien
Gelman, Laurent
Roth, Gregory
Nora, Elphège P.
Tiana, Guido
Giorgetti, Luca
author_sort Mach, Pia
collection PubMed
description In mammals, interactions between sequences within topologically associating domains enable control of gene expression across large genomic distances. Yet it is unknown how frequently such contacts occur, how long they last and how they depend on the dynamics of chromosome folding and loop extrusion activity of cohesin. By imaging chromosomal locations at high spatial and temporal resolution in living cells, we show that interactions within topologically associating domains are transient and occur frequently during the course of a cell cycle. Interactions become more frequent and longer in the presence of convergent CTCF sites, resulting in suppression of variability in chromosome folding across time. Supported by physical models of chromosome dynamics, our data suggest that CTCF-anchored loops last around 10 min. Our results show that long-range transcriptional regulation might rely on transient physical proximity, and that cohesin and CTCF stabilize highly dynamic chromosome structures, facilitating selected subsets of chromosomal interactions.
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spelling pubmed-97291132022-12-09 Cohesin and CTCF control the dynamics of chromosome folding Mach, Pia Kos, Pavel I. Zhan, Yinxiu Cramard, Julie Gaudin, Simon Tünnermann, Jana Marchi, Edoardo Eglinger, Jan Zuin, Jessica Kryzhanovska, Mariya Smallwood, Sebastien Gelman, Laurent Roth, Gregory Nora, Elphège P. Tiana, Guido Giorgetti, Luca Nat Genet Article In mammals, interactions between sequences within topologically associating domains enable control of gene expression across large genomic distances. Yet it is unknown how frequently such contacts occur, how long they last and how they depend on the dynamics of chromosome folding and loop extrusion activity of cohesin. By imaging chromosomal locations at high spatial and temporal resolution in living cells, we show that interactions within topologically associating domains are transient and occur frequently during the course of a cell cycle. Interactions become more frequent and longer in the presence of convergent CTCF sites, resulting in suppression of variability in chromosome folding across time. Supported by physical models of chromosome dynamics, our data suggest that CTCF-anchored loops last around 10 min. Our results show that long-range transcriptional regulation might rely on transient physical proximity, and that cohesin and CTCF stabilize highly dynamic chromosome structures, facilitating selected subsets of chromosomal interactions. Nature Publishing Group US 2022-12-05 2022 /pmc/articles/PMC9729113/ /pubmed/36471076 http://dx.doi.org/10.1038/s41588-022-01232-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mach, Pia
Kos, Pavel I.
Zhan, Yinxiu
Cramard, Julie
Gaudin, Simon
Tünnermann, Jana
Marchi, Edoardo
Eglinger, Jan
Zuin, Jessica
Kryzhanovska, Mariya
Smallwood, Sebastien
Gelman, Laurent
Roth, Gregory
Nora, Elphège P.
Tiana, Guido
Giorgetti, Luca
Cohesin and CTCF control the dynamics of chromosome folding
title Cohesin and CTCF control the dynamics of chromosome folding
title_full Cohesin and CTCF control the dynamics of chromosome folding
title_fullStr Cohesin and CTCF control the dynamics of chromosome folding
title_full_unstemmed Cohesin and CTCF control the dynamics of chromosome folding
title_short Cohesin and CTCF control the dynamics of chromosome folding
title_sort cohesin and ctcf control the dynamics of chromosome folding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729113/
https://www.ncbi.nlm.nih.gov/pubmed/36471076
http://dx.doi.org/10.1038/s41588-022-01232-7
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