Evidence map›Paper›PMID 28059702›Full record

ArticleeLife2017

CDK-regulated dimerization of M18BP1 on a Mis18 hexamer is necessary for CENP-A loading.

Dongqing Pan, Kerstin Klare, Arsen Petrovic, Annika Take, Kai Walstein, Priyanka Singh, Arnaud Rondelet, Alexander W Bird, Andrea Musacchio

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

61 citing papers in PubMed, 96 citations in OpenAlex.

  1. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
  3. Dual Roads of CENP-A for Centromere Identification.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The CENP-A chaperone complex spatially organizes centromeres.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Preserving centromere identity: right amounts of CENP-A at the right place and time.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  13. A brief historical perspective on cell cycle control of CENP-A assembly and inheritance.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  14. Article
  15. Article
  16. Article
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1 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Dongqing PanDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Kerstin KlareDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Arsen PetrovicDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Annika TakeDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Kai WalsteinDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Priyanka SinghDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.
Arnaud RondeletDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0001-5816-4137
Alexander W BirdDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0002-1061-0799
Andrea MusacchioDepartment of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-2362-8784
Max Planck Institute of Molecular Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Centromeres are unique chromosomal loci that promote the assembly of kinetochores, macromolecular complexes that bind spindle microtubules during mitosis. In most organisms, centromeres lack defined genetic features. Rather, they are specified epigenetically by a centromere-specific histone H3 variant, CENP-A. The Mis18 complex, comprising the Mis18α:Mis18β subcomplex and M18BP1, is crucial for CENP-A homeostasis. It recruits the CENP-A-specific chaperone HJURP to centromeres and primes it for CENP-A loading. We report here that a specific arrangement of Yippee domains in a human Mis18α:Mis18β 4:2 hexamer binds two copies of M18BP1 through M18BP1's 140 N-terminal residues. Phosphorylation by Cyclin-dependent kinase 1 (CDK1) at two conserved sites in this region destabilizes binding to Mis18α:Mis18β, limiting complex formation to the G1 phase of the cell cycle. Using an improved viral 2A peptide co-expression strategy, we demonstrate that CDK1 controls Mis18 complex recruitment to centromeres by regulating oligomerization of M18BP1 through the Mis18α:Mis18β scaffold.

Indexed as

Protein MultimerizationAdaptor Proteins, Signal TransducingCDC2 Protein KinaseCell Cycle ProteinsCentromereCentromere Protein AChromosomal Proteins, Non-HistoneHumansPhosphorylationProtein BindingProtein Processing, Post-TranslationalAdaptor Proteins, Signal TransducingCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCentromere Protein AChromosomal Proteins, Non-HistoneMIS18A protein, humanMIS18BP1 protein, humanOIP5 protein, humanbiochemistrycell biologycell cycleCENP-Acentromerechromatinhumankinetochore

Identifiers

PMID28059702
PMCPMC5245964
OpenAlexW2569419841

What OpenQuestion holds

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LicenceCC BY
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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.