Evidence map›Paper›PMID 32027339›Full record

ArticleThe Journal of cell biology2020

Untangling the contribution of Haspin and Bub1 to Aurora B function during mitosis.

Michael A Hadders, Sanne Hindriksen, My Anh Truong, Aditya N Mhaskar, J Pepijn Wopken, Martijn J M Vromans, Susanne M A Lens

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. 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
7.8field-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

61 citing papers in PubMed, 99 citations in OpenAlex.

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  11. Haspin kinase binds to a nucleosomal DNA supergroove.Nature structural & molecular biology · 2025
    Article
  12. Article
  13. Histone H3 tail modifications required for meiosis inbioRxiv : the preprint server for biology · 2024
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  14. Article
  15. Article
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  18. Review
  19. Article
  20. Article

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

7 authors at 1 institution in 1 country.

Michael A Hadders *Oncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Sanne Hindriksen *Oncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
My Anh TruongOncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Aditya N MhaskarOncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
J Pepijn WopkenOncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Martijn J M VromansOncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Susanne M A LensOncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Utrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aurora B kinase is essential for faithful chromosome segregation during mitosis. During (pro)metaphase, Aurora B is concentrated at the inner centromere by the kinases Haspin and Bub1. However, how Haspin and Bub1 collaborate to control Aurora B activity at centromeres remains unclear. Here, we show that either Haspin or Bub1 activity is sufficient to recruit Aurora B to a distinct chromosomal locus. Moreover, we identified a small, Bub1 kinase-dependent Aurora B pool that supported faithful chromosome segregation in otherwise unchallenged cells. Joined inhibition of Haspin and Bub1 activities fully abolished Aurora B accumulation at centromeres. While this impaired the correction of erroneous KT-MT attachments, it did not compromise the mitotic checkpoint, nor the phosphorylation of the Aurora B kinetochore substrates Hec1, Dsn1, and Knl1. This suggests that Aurora B substrates at the kinetochore are not phosphorylated by centromere-localized pools of Aurora B, and calls for a reevaluation of the current spatial models for how tension affects Aurora B-dependent kinetochore phosphorylation.

Indexed as

Chromosome SegregationMitosisAurora Kinase BChromosomal Proteins, Non-HistoneCytoskeletal ProteinsHCT116 CellsHumansIntracellular Signaling Peptides and ProteinsKinesinsKinetochoresMicrotubule-Associated ProteinsMicrotubulesM Phase Cell Cycle CheckpointsPhosphorylationProtein Serine-Threonine KinasesSignal TransductionAURKB protein, humanAurora Kinase BBUB1 protein, humanChromosomal Proteins, Non-HistoneCytoskeletal ProteinsDSN1 protein, humanHASPIN protein, humanIntracellular Signaling Peptides and ProteinsKIF2C protein, humanKinesinsKnl1 protein, humanMicrotubule-Associated ProteinsNDC80 protein, humanProtein Serine-Threonine Kinases

Identifiers

PMID32027339
PMCPMC7054988
OpenAlexW3004761925

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.