Evidence map›Paper›PMID 30674583›Full record

ArticleThe Journal of cell biology2019

MAD1-dependent recruitment of CDK1-CCNB1 to kinetochores promotes spindle checkpoint signaling.

Tatiana Alfonso-Pérez, Daniel Hayward, James Holder, Ulrike Gruneberg, Francis A Barr

Open access · hybridAbstract readVideo-Audio Media
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 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.7field-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

57 citing papers in PubMed, 96 citations in OpenAlex.

  1. WEE1 opposes APC/CNature · 2026
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  5. 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

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

5 authors at 1 institution in 1 country.

Tatiana Alfonso-PérezDepartment of Biochemistry, University of Oxford, Oxford, UK.
Daniel HaywardSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
James HolderDepartment of Biochemistry, University of Oxford, Oxford, UK.
Ulrike GrunebergSir William Dunn School of Pathology, University of Oxford, Oxford, UK ulrike.gruneberg@path.ox.ac.uk.ORCID 0000-0001-8344-0500
Francis A BarrDepartment of Biochemistry, University of Oxford, Oxford, UK francis.barr@bioch.ox.ac.uk.ORCID 0000-0001-7518-253X
University of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M00354X/1Cancer Research UK 15940Cancer Research UK 24743Cancer Research UK C20079/A15940Medical Research Council MR/K006703/1
6 · The paper itself

Abstract

Cyclin B-dependent kinase (CDK1-CCNB1) promotes entry into mitosis. Additionally, it inhibits mitotic exit by activating the spindle checkpoint. This latter role is mediated through phosphorylation of the checkpoint kinase MPS1 and other spindle checkpoint proteins. We find that CDK1-CCNB1 localizes to unattached kinetochores and like MPS1 is lost from these structures upon microtubule attachment. This suggests that CDK1-CCNB1 is an integral component and not only an upstream regulator of the spindle checkpoint pathway. Complementary proteomic and cell biological analysis demonstrate that the spindle checkpoint protein MAD1 is one of the major components of CCNB1 complexes, and that CCNB1 is recruited to unattached kinetochores in an MPS1-dependent fashion through interaction with the first 100 amino acids of MAD1. This MPS1 and MAD1-dependent pool of CDK1-CCNB1 creates a positive feedback loop necessary for timely recruitment of MPS1 to kinetochores during mitotic entry and for sustained spindle checkpoint arrest. CDK1-CCNB1 is therefore an integral component of the spindle checkpoint, ensuring the fidelity of mitosis.

Indexed as

M Phase Cell Cycle CheckpointsSignal TransductionCDC2 Protein KinaseCell Cycle ProteinsCyclin B1HEK293 CellsHeLa CellsHumansKinetochoresProtein BindingProtein Serine-Threonine KinasesProtein-Tyrosine KinasesSpindle ApparatusTime FactorsCCNB1 protein, humanCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCyclin B1MAD1L1 protein, humanProtein Serine-Threonine KinasesProtein-Tyrosine KinasesTTK protein, human

Identifiers

PMID30674583
PMCPMC6446853
OpenAlexW2912278697

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.