Evidence map›Paper›PMID 25298395›Full record

ArticleThe EMBO journal2014

Inhibitor-3 ensures bipolar mitotic spindle attachment by limiting association of SDS22 with kinetochore-bound protein phosphatase-1.

Annika Eiteneuer, Jonas Seiler, Matthias Weith, Monique Beullens, Bart Lesage, Veronica Krenn, Andrea Musacchio, Mathieu Bollen, Hemmo Meyer

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Alternating binding and p97-mediated dissociation of SDS22 and I3 recycles active PP1 between holophosphatases.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Open biology · 2022
    Article
  7. Genes · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Protein phosphatases in the regulation of mitosis.The Journal of cell biology · 2019
    Review
  14. Review
  15. Article
  16. The structure of SDS22 provides insights into the mechanism of heterodimer formation with PP1.Acta crystallographica. Section F, Structural biology communications · 2018
    Article
  17. KNL1 Binding to PP1 and Microtubules Is Mutually Exclusive.Structure (London, England : 1993) · 2018
    Article
  18. Article
  19. Kinase and Phosphatase Cross-Talk at the Kinetochore.Frontiers in cell and developmental biology · 2018
    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

9 authors at 3 institutions in 2 countries.

Annika EiteneuerCentre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.
Jonas SeilerCentre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.
Matthias WeithCentre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.
Monique BeullensLaboratory of Biosignaling & Therapeutics, KU Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium.
Bart LesageLaboratory of Biosignaling & Therapeutics, KU Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium.
Veronica KrennDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Andrea MusacchioCentre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Mathieu BollenLaboratory of Biosignaling & Therapeutics, KU Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium.
Hemmo MeyerCentre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany hemmo.meyer@uni-due.de.
University of Duisburg-Essen · DEKU Leuven · BEMax Planck Institute of Molecular Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Faithful chromosome segregation during mitosis is tightly regulated by opposing activities of Aurora B kinase and protein phosphatase-1 (PP1). PP1 function at kinetochores has been linked to SDS22, but the exact localization of SDS22 and how it affects PP1 are controversial. Here, we confirm that SDS22 is required for PP1 activity, but show that SDS22 does not normally localize to kinetochores. Instead, SDS22 is kept in solution by formation of a ternary complex with PP1 and inhibitor-3 (I3). Depletion of I3 does not affect the amount of PP1 at kinetochores but causes quantitative association of SDS22 with PP1 on KNL1 at the kinetochore. Such accumulation of SDS22 at kinetochores interferes with PP1 activity and inhibits Aurora B threonine-232 dephosphorylation, which leads to increased Aurora B activity in metaphase and persistence in anaphase accompanied with segregation defects. We propose a model in which I3 regulates an SDS22-mediated PP1 activation step in solution that precedes SDS22 dissociation and transfer of PP1 to kinetochores, and which is required for PP1 to efficiently antagonize Aurora B.

Indexed as

Models, BiologicalAurora Kinase BHeLa CellsHumansIntracellular Signaling Peptides and ProteinsKinetochoresMultiprotein ComplexesPhosphorylationProtein Phosphatase 1Spindle ApparatusUbiquitin-Protein LigasesAURKB protein, humanAurora Kinase BIntracellular Signaling Peptides and ProteinsMultiprotein ComplexesPPP1R11 protein, humanPPP1R7 protein, humanProtein Phosphatase 1Ubiquitin-Protein LigasesAurora Bchromosome segregationkinetochoremitosisprotein phosphatase‐1

Identifiers

PMID25298395
PMCPMC4282577
OpenAlexW2120732964

What OpenQuestion holds

Textmetadata
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.