Evidence map›Paper›PMID 24120884›Full record

ArticleDevelopmental cell2013

DAF-2 and ERK couple nutrient availability to meiotic progression during Caenorhabditis elegans oogenesis.

Andrew L Lopez, Jessica Chen, Hyoe-Jin Joo, Melanie Drake, Miri Shidate, Cedric Kseib, Swathi Arur

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

57 citing papers in PubMed, 89 citations in OpenAlex.

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  17. Analysis of the C. elegans Germline Stem Cell Pool.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  18. Article
  19. Article
  20. Regulation of oocyte maturation: Role of conserved ERK signaling.Molecular reproduction and development · 2022
    Review
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.

Andrew L LopezDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Jessica ChenDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Hyoe-Jin JooDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Melanie DrakeDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Miri ShidateDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Cedric KseibDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Swathi ArurDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: sarur@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Erk-mediated regulation of Dicer and Drosha function in C. elegansR01GM098200 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ARUR, SWATHI · 2011 to 2020
$3.3M
NCI NIH HHS P30 CA016672NIGMS NIH HHS GM98200NIGMS NIH HHS R01 GM098200NIH HHS P40 OD010440
6 · The paper itself

Abstract

Coupling the production of mature gametes and fertilized zygotes to favorable nutritional conditions improves reproductive success. In invertebrates, the proliferation of female germline stem cells is regulated by nutritional status. However, in mammals, the number of female germline stem cells is set early in development, with oocytes progressing through meiosis later in life. Mechanisms that couple later steps of oogenesis to environmental conditions remain largely undefined. We show that, in the presence of food, the DAF-2 insulin-like receptor signals through the RAS-ERK pathway to drive meiotic prophase I progression and oogenesis; in the absence of food, the resultant inactivation of insulin-like signaling leads to downregulation of the RAS-ERK pathway, and oogenesis is stalled. Thus, the insulin-like signaling pathway couples nutrient sensing to meiotic I progression and oocyte production in C. elegans, ensuring that oocytes are only produced under conditions favorable for the survival of the resulting zygotes.

Indexed as

Meiotic Prophase IOogenesisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEnzyme ActivationForkhead Transcription FactorsMitogen-Activated Protein Kinase 1OocytesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, InsulinSignal TransductionTranscription FactorsAGE-1 protein, C elegansakt-1 protein, C elegansCaenorhabditis elegans Proteinsdaf-16 protein, C elegansDAF-2 protein, C elegansForkhead Transcription FactorsMitogen-Activated Protein Kinase 1mpk-1 protein, C elegansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, InsulinTranscription Factors

Identifiers

PMID24120884
PMCPMC3829605
OpenAlexW2037986190

What OpenQuestion holds

Textmetadata
LicenceTDM
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.