Evidence map›Paper›PMID 24120663›Full record

ArticleMolecular cell2013

The BEG (PP2A-B55/ENSA/Greatwall) pathway ensures cytokinesis follows chromosome separation.

Michael J Cundell, Ricardo Nunes Bastos, Tongli Zhang, James Holder, Ulrike Gruneberg, Bela Novak, Francis A Barr

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
7.3field-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

95 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
  2. FAM122A inhibition of PP2A-B55 through a bipartite binding mechanism.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. IL-22 regulates MASTL expression in intestinal epithelial cells.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  11. Article
  12. Greatwall-Endos-PP2A/B55Open biology · 2024
    Article
  13. Article
  14. Inducible degradation-coupled phosphoproteomics identifies PP2AFrontiers in cell and developmental biology · 2024
    Article
  15. Deficiency ofFrontiers in cell and developmental biology · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

35 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 J CundellUniversity of Oxford, Department of Biochemistry, South Parks Road, Oxford OX1 3QU, UK.
Ricardo Nunes Bastos
Tongli Zhang
James Holder
Ulrike Gruneberg
Bela Novak
Francis A Barr
University of Oxford · GB

Funding

Cancer Research UK 15940Cancer Research UK C20079/A15940Cancer Research UK C24085/A8296Wellcome Trust 091911
6 · The paper itself

Abstract

Cytokinesis follows separase activation and chromosome segregation. This order is ensured in budding yeast by the mitotic exit network (MEN), where Cdc14p dephosphorylates key conserved Cdk1-substrates exemplified by the anaphase spindle-elongation protein Ase1p. However, in metazoans, MEN and Cdc14 function is not conserved. Instead, the PP2A-B55α/ENSA/Greatwall (BEG) pathway controls the human Ase1p ortholog PRC1. In this pathway, PP2A-B55 inhibition is coupled to Cdk1-cyclin B activity, whereas separase inhibition is maintained by cyclin B concentration. This creates two cyclin B thresholds during mitotic exit. Simulation and experiments using PRC1 as a model substrate show that the first threshold permits separase activation and chromosome segregation, and the second permits PP2A-B55 activation and initiation of cytokinesis. Removal of the ENSA/Greatwall (EG) timer module eliminates this second threshold, as well as associated delay in PRC1 dephosphorylation and initiation of cytokinesis, by uncoupling PP2A-B55 from Cdk1-cyclin B activity. Therefore, temporal order during mitotic exit is promoted by the metazoan BEG pathway.

Indexed as

CDC2 Protein KinaseChromosomesChromosome SegregationCyclin BCytokinesisHeLa CellsHumansMicrotubule-Associated ProteinsMitosisPhosphoric Monoester HydrolasesProtein Phosphatase 2Protein Serine-Threonine KinasesProtein Tyrosine PhosphatasesSeparaseSignal TransductionCDC14A protein, humanCDC2 Protein KinaseCyclin BMASTL protein, humanMicrotubule-Associated ProteinsPhosphoric Monoester HydrolasesPPP2CA protein, humanPPP2R2A protein, humanProtein Phosphatase 2Protein Serine-Threonine KinasesProtein Tyrosine PhosphatasesSeparase

Identifiers

PMID24120663
PMCPMC3898901
OpenAlexW2033364305

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.