Evidence map›Paper›PMID 38168769›Full record

ArticleNature cell biology2024

Higher-order protein assembly controls kinetochore formation.

Gunter B Sissoko, Ekaterina V Tarasovetc, Océane Marescal, Ekaterina L Grishchuk, Iain M Cheeseman

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 40 years of CENP-A: the foundation of a new era of centromere biology.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Article
  10. Article
  11. Article
  12. The dynamics of centromere assembly and disassembly during quiescence.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Binding site maturation modulated by molecular density underlies Ndc80 binding to kinetochore receptor CENP-T.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. A noncanonical GTPase signaling mechanism controls exit from mitosis in budding yeast.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Article
  18. Article
  19. Review
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

5 authors at 2 institutions in 1 country.

Gunter B Sissoko *Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ekaterina V Tarasovetc *Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Océane MarescalWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ekaterina L GrishchukDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. gekate@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-9504-4270
Iain M CheesemanWhitehead Institute for Biomedical Research, Cambridge, MA, USA. icheese@wi.mit.edu.ORCID http://orcid.org/0000-0002-3829-5612
Whitehead Institute for Biomedical Research · USUniversity of Pennsylvania · US

Funding

Molecular Analysis of Kinetochore FunctionR35GM126930 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI Iain McPherson Cheeseman · 2018 to 2026
$7.0M
Biomechanics of molecular machines and multiscale non-linear systemsR35GM141747 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Ekaterina L Grishchuk · 2021 to 2026
$3.7M
NIGMS NIH HHS R35 GM126930NIGMS NIH HHS R35 GM141747
6 · The paper itself

Abstract

To faithfully segregate chromosomes during vertebrate mitosis, kinetochore-microtubule interactions must be restricted to a single site on each chromosome. Prior work on pair-wise kinetochore protein interactions has been unable to identify the mechanisms that prevent outer kinetochore formation in regions with a low density of CENP-A nucleosomes. To investigate the impact of higher-order assembly on kinetochore formation, we generated oligomers of the inner kinetochore protein CENP-T using two distinct, genetically engineered systems in human cells. Although individual CENP-T molecules interact poorly with outer kinetochore proteins, oligomers that mimic centromeric CENP-T density trigger the robust formation of functional, cytoplasmic kinetochore-like particles. Both in cells and in vitro, each molecule of oligomerized CENP-T recruits substantially higher levels of outer kinetochore components than monomeric CENP-T molecules. Our work suggests that the density dependence of CENP-T restricts outer kinetochore recruitment to centromeres, where densely packed CENP-A recruits a high local concentration of inner kinetochore proteins.

Indexed as

Chromosomal Proteins, Non-HistoneKinetochoresCentromereCentromere Protein AHumansMitosisNucleosomesCentromere Protein AChromosomal Proteins, Non-HistoneNucleosomes

Identifiers

PMID38168769
PMCPMC10842828
OpenAlexW4390501050

What OpenQuestion holds

Textmetadata
LicenceTDM
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.