Evidence map›Paper›PMID 41238959›Full record

ArticleNature genetics2025

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

Thomas Sabaté, Benoît Lelandais, Marie-Cécile Robert, Michael Szalay, Jean-Yves Tinevez, Edouard Bertrand, Christophe Zimmer

Abstract read
In one paragraph

Article in Nature genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Transcription and Three-Dimensional Genome Organization: Cause, Consequence, or Coordination?BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Review
  3. Review
  4. Genome-wide absolute quantification of chromatin looping.Nature structural & molecular biology · 2026
    Article
  5. Putting numbers on chromatin looping.Nature structural & molecular biology · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Thomas SabatéImaging and Modeling Unit, Institut Pasteur, Université Paris Cité, Paris, France. t.sabate@hubrecht.eu.ORCID http://orcid.org/0000-0001-8710-6956
Benoît Lelandais *Imaging and Modeling Unit, Institut Pasteur, Université Paris Cité, Paris, France.
Marie-Cécile Robert *Institut de Génétique Humaine, University of Montpellier, CNRS, Montpellier, France.ORCID http://orcid.org/0000-0003-1603-4187
Michael SzalayInstitut de Génétique Humaine, University of Montpellier, CNRS, Montpellier, France.
Jean-Yves TinevezImage Analysis Hub, Institut Pasteur, Université Paris Cité, Paris, France.ORCID http://orcid.org/0000-0002-0998-4718
Edouard BertrandInstitut de Génétique Humaine, University of Montpellier, CNRS, Montpellier, France. christophe.zimmer@pasteur.fr.ORCID http://orcid.org/0000-0002-9642-7994
Christophe ZimmerImaging and Modeling Unit, Institut Pasteur, Université Paris Cité, Paris, France. edouard.bertrand@igh.cnrs.fr.ORCID http://orcid.org/0000-0001-9910-1589

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-INBS-04Agence Nationale de la Recherche (French National Research Agency) ANR-16-CONV-0005Agence Nationale de la Recherche (French National Research Agency) ANR-24-EXCI-0002Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) ARCDOC 42021120004333
6 · The paper itself

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.

Indexed as

Cell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneBinding SitesCCCTC-Binding FactorCohesinsGenome, HumanHumansCCCTC-Binding FactorCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsCTCF protein, human

Identifiers

PMID41238959
PMCPMC12695666

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.