Evidence map›Paper›PMID 28004745›Full record

ArticleNature communications2016

PKCɛ switches Aurora B specificity to exit the abscission checkpoint.

Tanya Pike, Nicola Brownlow, Svend Kjaer, Jeremy Carlton, Peter J Parker

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  13. CDK11The Journal of biological chemistry · 2019
    Article
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  18. ESCRT-dependent control of membrane remodelling during cell division.Seminars in cell & developmental biology · 2018
    Review
  19. Article
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 2 institutions in 1 country.

Tanya PikeProtein Phosphorylation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Nicola BrownlowProtein Phosphorylation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Svend KjaerProtein Purification Facility, Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Jeremy CarltonDivision of Cancer Studies King's College London, New Hunt's House, Guy's Campus, London SE1 1UL, UK.
Peter J ParkerProtein Phosphorylation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
The Francis Crick Institute · GBKing's College London · GB

Funding

Cancer Research UK 15683Wellcome Trust FC001130
6 · The paper itself

Abstract

The 'NoCut', or Aurora B abscission checkpoint can be activated if DNA is retained in the cleavage furrow after completion of anaphase. Checkpoint failure leads to incomplete abscission and a binucleate outcome. These phenotypes are also observed after loss of PKCɛ in transformed cell models. Here we show that PKCɛ directly modulates the Aurora B-dependent abscission checkpoint by phosphorylating Aurora B at S227. This phosphorylation invokes a switch in Aurora B specificity, with increased phosphorylation of a subset of target substrates, including the CPC subunit Borealin. This switch is essential for abscission checkpoint exit. Preventing the phosphorylation of Borealin leads to abscission failure, as does expression of a non-phosphorylatable Aurora B S227A mutant. Further, depletion of the ESCRT-III component and Aurora B substrate CHMP4C enables abscission, bypassing the PKCɛ-Aurora B exit pathway. Thus, we demonstrate that PKCɛ signals through Aurora B to exit the abscission checkpoint and complete cell division.

Indexed as

Amino Acid SequenceAnaphaseAurora Kinase BCell Cycle CheckpointsCell Cycle ProteinsCell LineCytokinesisEndosomal Sorting Complexes Required for TransportHEK293 CellsHumansModels, BiologicalMutationPhosphorylationProtein Kinase C-epsilonRecombinant ProteinsSignal TransductionAURKB protein, humanAurora Kinase BCDCA8 protein, humanCell Cycle ProteinsCHMP4C protein, humanEndosomal Sorting Complexes Required for TransportPRKCE protein, humanProtein Kinase C-epsilonRecombinant Proteins

Identifiers

PMID28004745
PMCPMC5192180
OpenAlexW2561625550

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.