Evidence map›Paper›PMID 16912277›Full record

ArticleGenes & development2006

C. elegans GLA-3 is a novel component of the MAP kinase MPK-1 signaling pathway required for germ cell survival.

Ekaterini A Kritikou, Stuart Milstein, Pierre-Olivier Vidalain, Guillaume Lettre, Erica Bogan, Kimon Doukoumetzidis, Phillip Gray, Thomas G Chappell, Marc Vidal, Michael O Hengartner

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  4. Article
  5. Article
  6. Article
  7. Role of zinc in female reproduction.Biology of reproduction · 2021
    Review
  8. Article
  9. Article
  10. Cap-Independent mRNA Translation in Germ Cells.International journal of molecular sciences · 2019
    Review
  11. Article
  12. Zinc deficiency reduces fertility in C. elegans hermaphrodites and disrupts oogenesis and meiotic progression.Comparative biochemistry and physiology. Toxicology & pharmacology : CBP · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
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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

10 authors at 3 institutions in 2 countries.

Ekaterini A KritikouInstitute of Molecular Biology, University of Zurich, 8057 Zurich, Switzerland.
Stuart Milstein
Pierre-Olivier Vidalain
Guillaume Lettre
Erica Bogan
Kimon Doukoumetzidis
Phillip Gray
Thomas G Chappell
Marc Vidal
Michael O Hengartner
University of Zurich · CHDana-Farber Cancer Institute · USLife Science Zurich · CH

Funding

The C. elegans Interactome ProjectR01HG001715 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI HILL, DAVID E., ROTH, FREDERICK P · 1998 to 2010
$16.5M
Tumor Cell Biology Training ProgramT32CA009361 · NCI · DANA-FARBER CANCER INSTITUTE · PI GRAY, NATHANAEL SCHIANDER · 1985 to 2015
$8.9M
Integrated interactome mappingR33CA105405 · NCI · DANA-FARBER CANCER INSTITUTE · PI VIDAL, MARC · 2004 to 2006
$2.0M
NCI NIH HHS 1 R33 CA105405-01NCI NIH HHS 5 T32 CA09361-25NCI NIH HHS R33 CA105405NCI NIH HHS T32 CA009361NHGRI NIH HHS 5 R01 HG01715-07NHGRI NIH HHS R01 HG001715
6 · The paper itself

Abstract

During oocyte development in Caenorhabditis elegans, approximately half of all developing germ cells undergo apoptosis. While this process is evolutionarily conserved from worms to humans, the regulators of germ cell death are still largely unknown. In a genetic screen for novel genes involved in germline apoptosis in Caenorhabditis elegans, we identified and cloned gla-3. Loss of gla-3 function results in increased germline apoptosis and reduced brood size due to defective pachytene exit from meiosis I. gla-3 encodes a TIS11-like zinc-finger-containing protein that is expressed in the germline, from the L4 larval stage to adulthood. Biochemical evidence and genetic epistasis analysis revealed that GLA-3 participates in the MAPK signaling cascade and directly interacts with the C. elegans MAPK MPK-1, an essential meiotic regulator. Our results show that GLA-3 is a new component of the MAPK cascade that controls meiotic progression and apoptosis in the C. elegans germline and functions as a negative regulator of the MAPK signaling pathway during vulval development and in muscle cells.

Indexed as

Cell SurvivalAnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsFemaleGerm CellsMaleMAP Kinase Signaling SystemMeiosisMitogen-Activated Protein Kinase 1Molecular Sequence DataMuscle CellsMutagenesisMutationProtein Interaction MappingCaenorhabditis elegans ProteinsGLA-3 protein, C elegansMitogen-Activated Protein Kinase 1mpk-1 protein, C elegansProtein Serine-Threonine KinasesTristetraprolin

Identifiers

PMID16912277
PMCPMC1553210
OpenAlexW2122665512

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.