Evidence map›Paper›PMID 32202322›Full record

ArticleThe EMBO journal2020

Cyclin B1 scaffolds MAD1 at the kinetochore corona to activate the mitotic checkpoint.

Lindsey A Allan, Magda Camacho Reis, Giuseppe Ciossani, Pim J Huis In 't Veld, Sabine Wohlgemuth, Geert Jpl Kops, Andrea Musacchio, Adrian T Saurin

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 85 citations in OpenAlex.

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  10. Countervailing effects of cyclin isoforms A and B during mitosis.bioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Lindsey A AllanDivision of Cellular Medicine, School of Medicine, University of Dundee, Dundee, UK.
Magda Camacho ReisDivision of Cellular Medicine, School of Medicine, University of Dundee, Dundee, UK.
Giuseppe CiossaniDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Pim J Huis In 't VeldDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-0234-6390
Sabine WohlgemuthDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Geert Jpl KopsOncode Institute, Hubrecht Institute-KNAW and University Medical Centre Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-3555-5295
Andrea MusacchioDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-2362-8784
Adrian T SaurinDivision of Cellular Medicine, School of Medicine, University of Dundee, Dundee, UK.ORCID 0000-0001-9317-2255
Max Planck Institute of Molecular Physiology · DEUniversity of Dundee · GBOncode Institute · NL

Funding

Cancer Research UK 21229
6 · The paper itself

Abstract

Cyclin B:CDK1 is the master kinase regulator of mitosis. We show here that, in addition to its kinase functions, mammalian Cyclin B also scaffolds a localised signalling pathway to help preserve genome stability. Cyclin B1 localises to an expanded region of the outer kinetochore, known as the corona, where it scaffolds the spindle assembly checkpoint (SAC) machinery by binding directly to MAD1. In vitro reconstitutions map the key binding interface to a few acidic residues in the N-terminal region of MAD1, and point mutations in this sequence abolish MAD1 corona localisation and weaken the SAC. Therefore, Cyclin B1 is the long-sought-after scaffold that links MAD1 to the corona, and this specific pool of MAD1 is needed to generate a robust SAC response. Robustness arises because Cyclin B1:MAD1 localisation loses dependence on MPS1 kinase after the corona has been established, ensuring that corona-localised MAD1 can still be phosphorylated when MPS1 activity is low. Therefore, this study explains how corona-MAD1 generates a robust SAC signal, and it reveals a scaffolding role for the key mitotic kinase, Cyclin B1:CDK1, which ultimately helps to inhibit its own degradation.

Indexed as

Cell Cycle CheckpointsMitosisCDC2 Protein KinaseCell Cycle ProteinsCyclin B1HeLa CellsHumansKinetochoresPoint MutationProtein DomainsCCNB1 protein, humanCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCyclin B1MAD1L1 protein, humanCyclin B1kinetochore coronaMADRZZ complexspindle assembly checkpoint

Identifiers

PMID32202322
PMCPMC7298293
OpenAlexW3012583628

What OpenQuestion holds

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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.