Evidence map›Paper›PMID 24794442›Full record

ArticleCell reports2014

Escargot restricts niche cell to stem cell conversion in the Drosophila testis.

Justin Voog, Sharsti L Sandall, Gary R Hime, Luís Pedro F Resende, Mariano Loza-Coll, Aaron Aslanian, John R Yates, Tony Hunter, Margaret T Fuller, D Leanne Jones

Abstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Lin28 Represses Hub Cell microRNAs to MaintainDevelopment & reproduction · 2026
    Review
  2. Niche-dependent modular regulation of the stem cell transcriptome separates cell identity and potential.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Preferential Solvation by Trifluoroethanol Drives α-Helical Folding in the Disordered S2 Region of the Escargot Protein.Chemphyschem : a European journal of chemical physics and physical chemistry · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Canonical and non-canonical functions of STAT in germline stem cell maintenance.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
  13. Article
  14. Article
  15. Single-cell transcriptome sequencing revealsProceedings. Biological sciences · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  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

10 authors.

Justin VoogDepartment of Biomedical Sciences, University of California, San Diego, La Jolla, CA, 92037, USA; Laboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Sharsti L SandallLaboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Gary R HimeARC Centre of Excellence in Biotechnology and Development, University of Melbourne, VIC 3010, Australia; Department of Anatomy and Neuroscience, University of Melbourne, VIC 3010, Australia.
Luís Pedro F ResendeLaboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA; GABBA, Instituto Ciências Biomédicas Abel Salazar, University of Porto, Portugal.
Mariano Loza-CollLaboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Aaron AslanianMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, 92037, USA.
John R YatesDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Tony HunterMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, 92037, USA.
Margaret T FullerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA, 94305, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA, 94305, USA.
D Leanne JonesLaboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, 90095, USA. Electronic address: leannejones@ucla.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007198 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHI, NEIL C, INSEL, PAUL A · 1985 to 2024
$29.3M
ZDS2P REGULATES SWE1P-DEPENDENT POLARIZED CELL GROWTH IN S CEREVISIAEP41RR011823 · NCRR · UNIVERSITY OF WASHINGTON · PI DAVIS, TRACY · 1996 to 2011
$24.7M
TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
SOMATIC CELL CYCLE REGULATION BY PHOSPHORYLATIONR01CA080100 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HUNTER, TONY R. · 1999 to 2018
$13.1M
Regulation of Stem Cell Self-Renewal and DifferentiationR01GM080501 · NIGMS · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2007 to 2019
$3.8M
Characterization of Age-Related Changes in Stem Cell BehaviorR01AG028092 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE · 2007 to 2016
$3.6M
Metabolic regulation of stem cell behavior and longevityR01AG040288 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE, WALKER, DAVID W · 2012 to 2016
$3.0M
NCI NIH HHS CA14915NCI NIH HHS CA80100NCI NIH HHS R01 CA080100NCRR NIH HHS 5P41RR011823-17NCRR NIH HHS P41 RR011823NIA NIH HHS R01 AG028092NIA NIH HHS R01 AG040288NIGMS NIH HHS 8P41GM103533-17NIGMS NIH HHS GM080501NIGMS NIH HHS P41 GM103533NIGMS NIH HHS R01 GM080501NIGMS NIH HHS T32 GM007198
6 · The paper itself

Abstract

Stem cells reside within specialized microenvironments, or niches, that control many aspects of stem cell behavior. Somatic hub cells in the Drosophila testis regulate the behavior of cyst stem cells (CySCs) and germline stem cells (GSCs) and are a primary component of the testis stem cell niche. The shutoff (shof) mutation, characterized by premature loss of GSCs and CySCs, was mapped to a locus encoding the evolutionarily conserved transcription factor Escargot (Esg). Hub cells depleted of Esg acquire CySC characteristics and differentiate as cyst cells, resulting in complete loss of hub cells and eventually CySCs and GSCs, similar to the shof mutant phenotype. We identified Esg-interacting proteins and demonstrate an interaction between Esg and the corepressor C-terminal binding protein (CtBP), which was also required for maintenance of hub cell fate. Our results indicate that niche cells can acquire stem cell properties upon removal of a single transcription factor in vivo.

Indexed as

Stem Cell NicheAllelesAnimalsCell LineageDrosophilaDrosophila ProteinsGerm CellsMaleStem CellsTestisTranscription FactorsDrosophila Proteinsesg protein, DrosophilaTranscription Factors

Identifiers

PMID24794442
PMCPMC4128242

What OpenQuestion holds

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Registered trials

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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.