Evidence map›Paper›PMID 20733051›Full record

ArticleThe Journal of cell biology2010

How cyclin A destruction escapes the spindle assembly checkpoint.

Barbara Di Fiore, Jonathon Pines

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

66 citing papers in PubMed, 100 citations in OpenAlex.

  1. Review
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  6. Cryo-EM structures of apo-APC/C and APC/CNature communications · 2024
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6 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

2 authors at 2 institutions in 1 country.

Barbara Di FioreWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, England, UK.
Jonathon Pines
Wellcome/Cancer Research UK Gurdon Institute · GBWellcome Trust · GB

Funding

Cancer Research UKWellcome Trust
6 · The paper itself

Abstract

The anaphase-promoting complex/cyclosome (APC/C) is the ubiquitin ligase essential to mitosis, which ensures that specific proteins are degraded at specific times to control the order of mitotic events. The APC/C coactivator, Cdc20, is targeted by the spindle assembly checkpoint (SAC) to restrict APC/C activity until metaphase, yet early substrates, such as cyclin A, are degraded in the presence of the active checkpoint. Cdc20 and the cyclin-dependent kinase cofactor, Cks, are required for cyclin A destruction, but how they enable checkpoint-resistant destruction has not been elucidated. In this study, we answer this problem: we show that the N terminus of cyclin A binds directly to Cdc20 and with sufficient affinity that it can outcompete the SAC proteins. Subsequently, the Cks protein is necessary and sufficient to promote cyclin A degradation in the presence of an active checkpoint by binding cyclin A-Cdc20 to the APC/C.

Indexed as

Anaphase-Promoting Complex-CyclosomeAnimalsCarrier ProteinsCdc20 ProteinsCDC2-CDC28 KinasesCell CycleCell Cycle ProteinsCyclin ACyclin-Dependent KinasesHeLa CellsHumansProtein BindingProtein Serine-Threonine KinasesRecombinant Fusion ProteinsRNA, Small InterferingSpindle ApparatusAnaphase-Promoting Complex-CyclosomeBub1 spindle checkpoint proteinCarrier ProteinsCDC20 protein, humanCdc20 ProteinsCDC2-CDC28 KinasesCell Cycle ProteinsCKS1B protein, humanCyclin ACyclin-Dependent KinasesProtein Serine-Threonine KinasesRecombinant Fusion ProteinsRNA, Small InterferingUbiquitin-Protein Ligase Complexes

Identifiers

PMID20733051
PMCPMC2928024
OpenAlexW2169971419

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.