Evidence map›Paper›PMID 27784789›Full record

ArticleOpen biology2016

Coordinated regulation of the ESCRT-III component CHMP4C by the chromosomal passenger complex and centralspindlin during cytokinesis.

Luisa Capalbo, Ioanna Mela, Maria Alba Abad, A Arockia Jeyaprakash, J Michael Edwardson, Pier Paolo D'Avino

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Mechanics and regulation of cytokinetic abscission.Frontiers in cell and developmental biology · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Actin reduction by MsrB2 is a key component of the cytokinetic abscission checkpoint and prevents tetraploidy.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. The many functions of ESCRTs.Nature reviews. Molecular cell biology · 2020
    Review
  16. CDK11The Journal of biological chemistry · 2019
    Article
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Luisa CapalboDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK lc284@cam.ac.uk.
Ioanna MelaDepartment of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.
Maria Alba AbadWellcome Trust Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Michael Swann Building, Kings Buildings, Mayfield Road, Edinburgh EH9 3JR, UK.
A Arockia JeyaprakashWellcome Trust Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Michael Swann Building, Kings Buildings, Mayfield Road, Edinburgh EH9 3JR, UK.
J Michael EdwardsonDepartment of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.
Pier Paolo D'AvinoDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK ppd21@cam.ac.uk.ORCID 0000-0002-4773-6950
University of Cambridge · GBWellcome Centre for Cell Biology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J018236/1Cancer Research UK 12541Cancer Research UK C12296/A12541Wellcome TrustWellcome Trust 095822
6 · The paper itself

Abstract

The chromosomal passenger complex (CPC)-composed of Aurora B kinase, Borealin, Survivin and INCENP-surveys the fidelity of genome segregation throughout cell division. The CPC has been proposed to prevent polyploidy by controlling the final separation (known as abscission) of the two daughter cells via regulation of the ESCRT-III CHMP4C component. The molecular details are, however, still unclear. Using atomic force microscopy, we show that CHMP4C binds to and remodels membranes in vitro Borealin prevents the association of CHMP4C with membranes, whereas Aurora B interferes with CHMP4C's membrane remodelling activity. Moreover, we show that CHMP4C phosphorylation is not required for its assembly into spiral filaments at the abscission site and that two distinctly localized pools of phosphorylated CHMP4C exist during cytokinesis. We also characterized the CHMP4C interactome in telophase cells and show that the centralspindlin complex associates preferentially with unphosphorylated CHMP4C in cytokinesis. Our findings indicate that gradual dephosphorylation of CHMP4C triggers a 'relay' mechanism between the CPC and centralspindlin that regulates the timely distribution and activation of CHMP4C for the execution of abscission.

Indexed as

CytokinesisAurora Kinase BCell Cycle ProteinsCell MembraneEndosomal Sorting Complexes Required for TransportHeLa CellsHumansMicroscopy, Atomic ForceMicrotubule-Associated ProteinsPhosphorylationProtein BindingProtein Interaction MapsSpindle ApparatusTelophaseAURKB protein, humanAurora Kinase BCDCA8 protein, humanCell Cycle ProteinsCHMP4C protein, humanEndosomal Sorting Complexes Required for TransportMicrotubule-Associated ProteinsAurora Bcell divisioncentralspindlincytokinesismembrane remodellingmidbody

Identifiers

PMID27784789
PMCPMC5090064
OpenAlexW2535513496

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.