Evidence map›Paper›PMID 41872526›Full record

ArticleThe EMBO journal2026

Condensin loop extrusion properties, roadblocks, and role in homology search during recombination in S. cerevisiae.

Vinciane Piveteau, Chloé Dupont, Hossein Salari, Agnès Dumont, Jérôme Savocco, Daniel Jost, Aurèle Piazza

Abstract read
In one paragraph

Article in The EMBO journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. How cohesin guides DNA repair via scanning and tethering.Nature structural & molecular biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Condensin Accelerates Long-Range Intra-Chromosomal Interactions.bioRxiv : the preprint server for biology · 2025
    Article
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.

Vinciane Piveteau *Université de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.ORCID http://orcid.org/0009-0006-1868-1942
Chloé Dupont *Université de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.ORCID http://orcid.org/0000-0002-2291-0772
Hossein SalariUniversité de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.ORCID http://orcid.org/0000-0001-8967-9264
Agnès DumontUniversité de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.
Jérôme SavoccoUniversité de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.ORCID http://orcid.org/0000-0003-0989-9473
Daniel JostUniversité de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France.ORCID http://orcid.org/0000-0002-9877-6864
Aurèle PiazzaUniversité de Lyon, ENS de Lyon, Université Claude Bernard, CNRS UMR5239, Laboratoire de Biologie et Modélisation de la Cellule, Lyon, France. aurele.piazza@ens-lyon.fr.ORCID http://orcid.org/0000-0002-7722-0955

Funding

Agence Nationale de la Recherche (ANR) ANR-23-CE12-0014-02European Commission (EC) 851006Fondation ARC pour la Recherche sur le Cancer (ARC) ARCPGA2022110005583_6379
6 · The paper itself

Abstract

The in vivo mechanism, cis-acting roadblocks, and biological functions of DNA loop extrusion by eukaryotic SMC complexes remain incompletely defined. Here, we identify condensin-dependent Hi-C contact stripes at the recombination enhancer (RE) and at rDNA in S. cerevisiae. The RE is an autonomous condensin loading site only active in MATa cells from which oriented, unidirectional loop extrusion proceeds with an estimated processivity ~150-250 kb and a density ~0.04-0.18 that varies across the cell cycle. Centromeres, replication forks, and highly transcribed RNA PolII-dependent genes represent roadblocks for condensin. Cohesin is not an obstacle for condensin, while Top2 promotes its loop extrusion activity. A DNA double-strand break (DSB) at MAT blocks loop extrusion, resulting in the establishment of a ~170 kb-long RE-MAT loop. The RE and the DSB are required and sufficient to form this site-specific loop, which promotes RE-proximal homology identification in the early stages of recombinational DNA break-repair. We propose that juxtaposition of the broken MATa site and its target HMLα donor is the relevant structure by which condensin promotes a-to-α mating-type switching.

Indexed as

Adenosine TriphosphatasesDNA-Binding ProteinsDNA, FungalMultiprotein ComplexesRecombination, GeneticSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA Breaks, Double-StrandedDNA, RibosomalAdenosine TriphosphatasesCell Cycle ProteinsChromosomal Proteins, Non-Histonecondensin complexesDNA-Binding ProteinsDNA, FungalDNA, RibosomalMultiprotein ComplexesSaccharomyces cerevisiae ProteinsCondensinHomology searchLoop extrusionMating-type switchingSMC

Identifiers

PMID41872526
PMCPMC13144730

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.