Evidence map›Paper›PMID 31676716›Full record

ArticleThe Journal of cell biology2019

CDK1-mediated CENP-C phosphorylation modulates CENP-A binding and mitotic kinetochore localization.

Reito Watanabe, Masatoshi Hara, Ei-Ichi Okumura, Solène Hervé, Daniele Fachinetti, Mariko Ariyoshi, Tatsuo Fukagawa

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  3. Dual Roads of CENP-A for Centromere Identification.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  11. 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
  12. Article
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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 at 3 institutions in 2 countries.

Reito Watanabe *Graduate School of Frontier Biosciences, Osaka University, Osaka, Japan.ORCID 0000-0003-3593-9045
Masatoshi Hara *Graduate School of Frontier Biosciences, Osaka University, Osaka, Japan mahara@fbs.osaka-u.ac.jp.ORCID 0000-0001-8433-1111
Ei-Ichi OkumuraLaboratory of Cell and Developmental Biology, Graduate School of Bioscience, Tokyo Institute of Technology, Yokohama, Japan.ORCID 0000-0001-9399-075X
Solène HervéInstitute Curie, Paris Sciences et Lettres Research University, Centre national de la recherche scientifique, UMR 144, Paris, France.
Daniele FachinettiInstitute Curie, Paris Sciences et Lettres Research University, Centre national de la recherche scientifique, UMR 144, Paris, France.ORCID 0000-0002-8795-6771
Mariko AriyoshiGraduate School of Frontier Biosciences, Osaka University, Osaka, Japan.
Tatsuo FukagawaGraduate School of Frontier Biosciences, Osaka University, Osaka, Japan tfukagawa@fbs.osaka-u.ac.jp.ORCID 0000-0001-8564-6852
Ube Frontier University · JPUniversité Paris Sciences et Lettres · FRTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kinetochore is essential for faithful chromosome segregation during mitosis. To form a functional kinetochore, constitutive centromere-associated network (CCAN) proteins are assembled on the centromere chromatin that contains the centromere-specific histone CENP-A. CENP-C, a CCAN protein, directly interacts with the CENP-A nucleosome to nucleate the kinetochore structure. As CENP-C is a hub protein for kinetochore assembly, it is critical to address how the CENP-A-CENP-C interaction is regulated during cell cycle progression. To address this question, we investigated the CENP-C C-terminal region, including a conserved CENP-A-binding motif, in both chicken and human cells and found that CDK1-mediated phosphorylation of CENP-C facilitates its binding to CENP-A in vitro and in vivo. We observed that CENP-A binding is involved in CENP-C kinetochore localization during mitosis. We also demonstrate that the CENP-A-CENP-C interaction is critical for long-term viability in human RPE-1 cells. These results provide deeper insights into protein-interaction network plasticity in centromere proteins during cell cycle progression.

Indexed as

AnimalsCDC2 Protein KinaseCentromereCentromere Protein AChickensChromosomal Proteins, Non-HistoneCyclin BCytoskeletal ProteinsFemaleHumansKinetochoresMitosisMutationOocytesPhosphorylationProtein BindingCDC2 Protein KinaseCDK1 protein, humanCentromere Protein Acentromere protein CChromosomal Proteins, Non-HistoneCyclin BCytoskeletal ProteinsNDC80 protein, humanRecombinant Proteins

Identifiers

PMID31676716
PMCPMC6891089
OpenAlexW2987220166

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.