Evidence map›Paper›PMID 21878498›Full record

ArticleJournal of cell science2011

Protein phosphatase 5 is a negative regulator of separase function during cortical granule exocytosis in C. elegans.

Christopher T Richie, Joshua N Bembenek, Barry Chestnut, Tokiko Furuta, Jill M Schumacher, Matthew Wallenfang, Andy Golden

Abstract read
In one paragraph

Article in Journal of cell science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. The embryonic lethal mutationmicroPublication biology · 2025
    Article
  4. Securin Regulates the Spatiotemporal Dynamics of Separase.bioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. C. elegans as a model for membrane traffic.WormBook : the online review of C. elegans biology · 2014
    Review
  16. 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

7 authors at 4 institutions in 1 country.

Christopher T RichieLaboratory of Biochemistry and Genetics, NIDDK, NIH, Bethesda, MD 20892, USA.
Joshua N Bembenek
Barry Chestnut
Tokiko Furuta
Jill M Schumacher
Matthew Wallenfang
Andy Golden
National Institutes of Health · USThe University of Texas MD Anderson Cancer Center · USBarnard College · USUniversity of Wisconsin–Madison · US

Funding

THE AIR-2 KINASE PATHWAY AND CYTOKINESIS IN C ELEGANSR01GM062181 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SCHUMACHER, JILL M · 2001 to 2009
$2.4M
Cell Cycle Regulation In C. elegansZIADK024947 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GOLDEN, ANDY · 2009 to 2012
$1.1M
The characterization of separase suppressorsZIADK024959 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GOLDEN, ANDY · 2009 to 2011
$367k
Intramural NIH HHSNIGMS NIH HHS 5R01GM062181NIGMS NIH HHS R01 GM062181
6 · The paper itself

Abstract

Mutations in the Caenorhabditis elegans separase gene, sep-1, are embryonic lethal. Newly fertilized mutant embryos have defects in polar body extrusion, fail to undergo cortical granule exocytosis, and subsequently fail to complete cytokinesis. Chromosome nondisjunction during the meiotic divisions is readily apparent after depletion of sep-1 by RNAi treatment, but much less so in hypomorphic mutant embryos. To identify factors that influence the activity of separase in cortical granule exocytosis and cytokinesis, we carried out a genetic suppressor screen. A mutation in the protein phosphatase 5 (pph-5) gene was identified as an extragenic suppressor of sep-1. This mutation suppressed the phenotypes of hypomorphic separase mutants but not RNAi depleted animals. Depletion of pph-5 caused no phenotypes on its own, but was effective in restoring localization of mutant separase to vesicles and suppressing cortical granule exocytosis and cytokinesis phenotypes. The identification of PPH-5 as a suppressor of separase suggests that a new phospho-regulatory pathway plays an important role in regulating anaphase functions of separase.

Indexed as

AllelesAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsCytokinesisCytoplasmic GranulesEndopeptidasesExocytosisMutationNuclear ProteinsPhosphoprotein PhosphatasesSeparaseCaenorhabditis elegans ProteinsCell Cycle ProteinsEndopeptidasesNuclear ProteinsPhosphoprotein Phosphatasesprotein phosphatase 5SEP-1 protein, C elegansSeparase

Identifiers

PMID21878498
PMCPMC3166036
OpenAlexW2107899731

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.