Evidence map›Paper›PMID 37976091›Full record

ArticleThe Journal of cell biology2024

Bridging condensins mediate compaction of mitotic chromosomes.

Giada Forte, Lora Boteva, Filippo Conforto, Nick Gilbert, Peter R Cook, Davide Marenduzzo

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Condensin-Condensin Interactions Facilitate Mitotic Chromosome Assembly in Xenopus Egg Extracts.Genes to cells : devoted to molecular & cellular mechanisms · 2025
    Article
  6. Article
  7. Mitotic genome folding.The Journal of cell biology · 2025
    Review
  8. Article
  9. Article
  10. Energy landscape analysis of the development of the chromosome structure across the cell cycle.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Helical coiled nucleosome chromosome architectures during cell cycle progression.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. 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

6 authors at 3 institutions in 1 country.

Giada ForteSchool of Physics and Astronomy, University of Edinburgh, Edinburgh, UK.
Lora BotevaMRC Human Genetics Unit, Western General Hospital, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.ORCID 0009-0001-1332-3939
Filippo ConfortoSchool of Physics and Astronomy, University of Edinburgh, Edinburgh, UK.ORCID 0009-0006-2859-1131
Nick GilbertMRC Human Genetics Unit, Western General Hospital, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-0505-6081
Peter R CookSir William Dunn School of Pathology, University of Oxford, Oxford, UK.ORCID 0000-0002-6639-188X
Davide MarenduzzoSchool of Physics and Astronomy, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-3974-4915
UK Astronomy Technology Centre · GBWestern General Hospital · GBUniversity of Oxford · GB

Funding

Wellcome TrustWellcome Trust 223097/Z/21/Z
6 · The paper itself

Abstract

Eukaryotic chromosomes compact during mitosis into elongated cylinders-and not the spherical globules expected of self-attracting long flexible polymers. This process is mainly driven by condensin-like proteins. Here, we present Brownian-dynamic simulations involving two types of such proteins with different activities. One, which we refer to as looping condensins, anchors long-lived chromatin loops to create bottlebrush structures. The second, referred to as bridging condensins, forms multivalent bridges between distant parts of these loops. We show that binding of bridging condensins leads to the formation of shorter and stiffer mitotic-like cylinders without requiring any additional energy input. These cylinders have several features matching experimental observations. For instance, the axial condensin backbone breaks up into clusters as found by microscopy, and cylinder elasticity qualitatively matches that seen in chromosome pulling experiments. Additionally, simulating global condensin depletion or local faulty condensin loading gives phenotypes seen experimentally and points to a mechanistic basis for the structure of common fragile sites in mitotic chromosomes.

Indexed as

Adenosine TriphosphatasesChromosomesDNA-Binding ProteinsMultiprotein ComplexesChromatinMitosisAdenosine TriphosphatasesChromatincondensin complexesDNA-Binding ProteinsMultiprotein Complexes

Identifiers

PMID37976091
PMCPMC10655892
OpenAlexW4388760660

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.