Evidence map›Paper›PMID 35165266›Full record

ArticleNature communications2022

Recruitment of two Ndc80 complexes via the CENP-T pathway is sufficient for kinetochore functions.

Yusuke Takenoshita, Masatoshi Hara, Tatsuo Fukagawa

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
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  13. Review
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  15. Structure of the human outer kinetochore KMN network complex.Nature structural & molecular biology · 2024
    Article
  16. Article
  17. Article
  18. CENP-I directly targets centromeric DNA to support CENP-A deposition and centromere maintenance.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Heterochromatin and RNAi act independently to ensure genome stability in Mucorales human fungal pathogens.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Cell cycle control of kinetochore assembly.Nucleus (Austin, Tex.) · 2022
    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

3 authors at 1 institution in 1 country.

Yusuke TakenoshitaGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID http://orcid.org/0000-0002-0720-815X
Masatoshi HaraGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID http://orcid.org/0000-0001-8433-1111
Tatsuo FukagawaGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan. tfukagawa@fbs.osaka-u.ac.jp.ORCID http://orcid.org/0000-0001-8564-6852
The University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To form functional kinetochores, CENP-C and CENP-T independently recruit the KMN (Knl1C, Mis12C, and Ndc80C) network onto the kinetochores. To clarify the functions of the KMN network on CENP-T, we evaluated its roles in chicken DT40 cell lines lacking the CENP-C-KMN network interaction. By analyzing mutants lacking both CENP-T-Mis12C and CENP-C-Mis12C interactions, we demonstrated that Knl1C and Mis12C (KM) play critical roles in the cohesion of sister chromatids or the recruitment of spindle checkpoint proteins onto kinetochores. Two copies of Ndc80C (N-N) exist on CENP-T via Mis12C or direct binding. Analyses of cells specifically lacking the Mis12C-Ndc80C interaction revealed that N-N is needed for proper kinetochore-microtubule interactions. However, using artificial engineering to directly bind the two copies of Ndc80C to CENP-T, we demonstrated that N-N functions without direct Mis12C binding to Ndc80C in native kinetochores. This study demonstrated the mechanisms by which complicated networks play roles in native kinetochores.

Indexed as

AnimalsCell LineChickensChromatidsChromosomal Proteins, Non-HistoneChromosome SegregationCytoskeletal ProteinsHumansKinetochoresMicrotubule-Associated ProteinsM Phase Cell Cycle CheckpointsCENPT protein, humancentromere protein CChromosomal Proteins, Non-HistoneCytoskeletal ProteinsMicrotubule-Associated ProteinsNDC80 protein, human

Identifiers

PMID35165266
PMCPMC8844409
OpenAlexW4212943054

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.