Uniform dynamics of cohesin-mediated loop extrusion in living human cells

Most animal genomes are partitioned into topologically associating domains (TADs), created by cohesin-mediated loop extrusion and defined by convergently oriented CCCTC-binding factor (CTCF) sites. The dynamics of loop extrusion and its regulation remain poorly characterized in vivo. Here we tracked the motion of TAD anchors in living human cells to visualize and quantify cohesin-dependent loop extrusion across multiple endogenous genomic regions. We show that TADs are dynamic structures whose anchors are brought in proximity about once per hour and for 6-19 min (~16% of the time). Moreover, TADs are continuously extruded by multiple cohesin complexes. Remarkably, despite strong differences in Hi-C patterns across chromatin regions, their dynamics is consistent with the same density, residence time and speed of cohesin. Our results suggest that TAD dynamics is primarily governed by the location and affinity of CTCF sites, enabling genome-wide predictive models of cohesin-dependent chromatin interactions.

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Publication Details

Journal
Nature Genetics
Published
2025-11-14
DOI
https://doi.org/10.1038/s41588-025-02406-9
Citations
5
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
4.03
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article

Uniform dynamics of cohesin-mediated loop extrusion in living human cells

Édouard Bertrand, Benoît Lelandais, Thomas Sabaté, Marie-Cécile Robert et al.
5 citations
Nature Genetics
Genomics and Chromatin Dynamics
4.03
article

Uniform dynamics of cohesin-mediated loop extrusion in living human cells

Édouard Bertrand, Benoît Lelandais, Thomas Sabaté, Marie-Cécile Robert, Jean-Yves Tinévez, Christophe Zimmer, Michael Szalay
article en
5 citations

Abstract

Most animal genomes are partitioned into topologically associating domains (TADs), created by cohesin-mediated loop extrusion and defined by convergently oriented CCCTC-binding factor (CTCF) sites. The dynamics of loop extrusion and its regulation remain poorly characterized in vivo. Here we tracked the motion of TAD anchors in living human cells to visualize and quantify cohesin-dependent loop extrusion across multiple endogenous genomic regions. We show that TADs are dynamic structures whose anchors are brought in proximity about once per hour and for 6-19 min (~16% of the time). Moreover, TADs are continuously extruded by multiple cohesin complexes. Remarkably, despite strong differences in Hi-C patterns across chromatin regions, their dynamics is consistent with the same density, residence time and speed of cohesin. Our results suggest that TAD dynamics is primarily governed by the location and affinity of CTCF sites, enabling genome-wide predictive models of cohesin-dependent chromatin interactions.

Nature GeneticsVol. 57(12)
Centre National de la Recherche Scientifique (FR), Institut Pasteur (FR), Université Sorbonne Nouvelle (FR), Université de Montpellier (FR), Université Paris Cité (FR), University of Würzburg (DE), Sorbonne Université (FR), Institut de Génétique Moléculaire de Montpellier (FR), Hubrecht Institute for Developmental Biology and Stem Cell Research (NL), Institut de Génétique Humaine (FR)
Openalex Percentile: Top 6%
Genomics and Chromatin Dynamics
4.03
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