Evidence map›Paper›PMID 34288923›Full record

ArticlePLoS genetics2021

DAF-18/PTEN inhibits germline zygotic gene activation during primordial germ cell quiescence.

Amanda L Fry, Amy K Webster, Julia Burnett, Rojin Chitrakar, L Ryan Baugh, E Jane Albert Hubbard

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. An atlas of thebioRxiv : the preprint server for biology · 2026
    Article
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  8. Article
  9. Germline stem cells in human.Signal transduction and targeted therapy · 2022
    Review
  10. Article
  11. 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.

Amanda L FrySkirball Institute of Biomolecular Medicine, Department of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.ORCID 0000-0003-4945-4540
Amy K WebsterDepartment of Biology, Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0003-4302-8102
Julia BurnettSkirball Institute of Biomolecular Medicine, Department of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.ORCID 0000-0003-0051-7694
Rojin ChitrakarDepartment of Biology, Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America.
L Ryan BaughDepartment of Biology, Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0003-2148-5492
E Jane Albert HubbardSkirball Institute of Biomolecular Medicine, Department of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.ORCID 0000-0001-5893-7232
Duke University · USNew York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
CONTROL ONSET OF MEIOSIS IN C. ELEGANSR01GM061706 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUBBARD, E. JANE ALBERT · 2000 to 2018
$5.4M
Systemic, maternal and transgenerational effects of nutrient stressR01GM117408 · NIGMS · DUKE UNIVERSITY · PI BAUGH, LARRY RYAN · 2015 to 2022
$2.5M
Diet and Germline ProgenitorsR35GM134876 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUBBARD, E. JANE ALBERT · 2020 to 2024
$2.1M
NCI NIH HHS P30 CA016087NIGMS NIH HHS R01 GM061706NIGMS NIH HHS R01 GM117408NIGMS NIH HHS R35 GM134876NIH HHS P40 OD010440
6 · The paper itself

Abstract

Quiescence, an actively-maintained reversible state of cell cycle arrest, is not well understood. PTEN is one of the most frequently lost tumor suppressors in human cancers and regulates quiescence of stem cells and cancer cells. The sole PTEN ortholog in Caenorhabditis elegans is daf-18. In a C. elegans loss-of-function mutant for daf-18, primordial germ cells (PGCs) divide inappropriately in L1 larvae hatched into starvation conditions, in a TOR-dependent manner. Here, we further investigated the role of daf-18 in maintaining PGC quiescence in L1 starvation. We found that maternal or zygotic daf-18 is sufficient to maintain cell cycle quiescence, that daf-18 acts in the germ line and soma, and that daf-18 affects timing of PGC divisions in fed animals. Importantly, our results also implicate daf-18 in repression of germline zygotic gene activation, though not in germline fate specification. However, TOR is less important to germline zygotic gene expression, suggesting that in the absence of food, daf-18/PTEN prevents inappropriate germline zygotic gene activation and cell division by distinct mechanisms.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle CheckpointsCell DivisionCell ProliferationGerm CellsLarvaPTEN PhosphohydrolaseSignal TransductionTranscriptional ActivationZygoteCaenorhabditis elegans ProteinsDAF-18 protein, C elegansPTEN Phosphohydrolase

Identifiers

PMID34288923
PMCPMC8294487
OpenAlexW3186363699

What OpenQuestion holds

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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.