Evidence map›Paper›PMID 35710836›Full record

ArticleNature structural & molecular biology2022

The cohesin acetylation cycle controls chromatin loop length through a PDS5A brake mechanism.

Marjon S van Ruiten, Démi van Gent, Ángela Sedeño Cacciatore, Astrid Fauster, Laureen Willems, Maarten L Hekkelman, Liesbeth Hoekman, Maarten Altelaar, Judith H I Haarhuis, Thijn R Brummelkamp and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Nature structural & molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.8field-weighted citation impact, top 3% of its field
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

47 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Cohesin acetylation and ATPase activity control cohesion and loop architecture through distinct mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. PDS5A and TOP2B cooperate for chromatin recruitment via CTCF.bioRxiv : the preprint server for biology · 2026
    Article
  12. Article
  13. Crosstalk BetweenCancers · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Clinical,medRxiv : the preprint server for health sciences · 2026
    Article
  19. Article
  20. 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

12 authors at 2 institutions in 1 country.

Marjon S van RuitenDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Démi van Gent *Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0001-8543-9036
Ángela Sedeño Cacciatore *Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0002-2751-0428
Astrid FausterDivision of Biochemistry, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Laureen WillemsDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Maarten L HekkelmanDivision of Biochemistry, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0002-9081-4707
Liesbeth HoekmanProteomics Facility, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Maarten AltelaarProteomics Facility, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Judith H I HaarhuisDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Thijn R BrummelkampDivision of Biochemistry, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Elzo de WitDivision of Gene Regulation, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0003-2883-1415
Benjamin D RowlandDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, the Netherlands. b.rowland@nki.nl.ORCID 0000-0002-0694-8463
The Netherlands Cancer Institute · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cohesin structures the genome through the formation of chromatin loops and by holding together the sister chromatids. The acetylation of cohesin's SMC3 subunit is a dynamic process that involves the acetyltransferase ESCO1 and deacetylase HDAC8. Here we show that this cohesin acetylation cycle controls the three-dimensional genome in human cells. ESCO1 restricts the length of chromatin loops, and of architectural stripes emanating from CTCF sites. HDAC8 conversely promotes the extension of such loops and stripes. This role in controlling loop length turns out to be distinct from the canonical role of cohesin acetylation that protects against WAPL-mediated DNA release. We reveal that acetylation controls the interaction of cohesin with PDS5A to restrict chromatin loop length. Our data support a model in which this PDS5A-bound state acts as a brake that enables the pausing and restart of loop enlargement. The cohesin acetylation cycle hereby provides punctuation in the process of genome folding.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneAcetylationChromatidsChromatinCohesinsHistone DeacetylasesHumansNuclear ProteinsRepressor ProteinsCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsHDAC8 protein, humanHistone DeacetylasesNuclear ProteinsPDS5A protein, humanRepressor Proteins

Identifiers

PMID35710836
PMCPMC9205776
OpenAlexW4283010781

What OpenQuestion holds

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LicenceCC BY
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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.