Evidence map›Paper›PMID 24991805›Full record

ArticlePloS one2014

Basolateral junction proteins regulate competition for the follicle stem cell niche in the Drosophila ovary.

Maria R Kronen, Kevin P Schoenfelder, Allon M Klein, Todd G Nystul

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Starve-Feed Cycles Direct Quiescence to Proliferation Transitions inbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Tracing the Dynamics of Stem Cell Fate.Cold Spring Harbor perspectives in biology · 2020
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Division-independent differentiation mandates proliferative competition among stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Review
  15. Neutral Competition forGenetics · 2017
    Article
  16. Article
  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

4 authors at 2 institutions in 1 country.

Maria R KronenUniversity of California, San Francisco, Center for Reproductive Sciences, Departments of Anatomy and OB/GYN-RS, San Francisco, California, United States of America.
Kevin P SchoenfelderUniversity of California, San Francisco, Center for Reproductive Sciences, Departments of Anatomy and OB/GYN-RS, San Francisco, California, United States of America.
Allon M KleinDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States of America.
Todd G NystulUniversity of California, San Francisco, Center for Reproductive Sciences, Departments of Anatomy and OB/GYN-RS, San Francisco, California, United States of America.
University of California, San Francisco · USCenter for Systems Biology · US

Funding

Modeling epithelial stem cell competition in a dynamic Drosophila ovarian nicheR01GM097158 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI NYSTUL, TODD · 2011 to 2019
$3.1M
Spinning disk confocal / FRAP microscope for quantitative live cell imagingS10RR026758 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTMANN, TORSTEN · 2010 to 2010
$500k
NCRR NIH HHS S10 RR026758NIGMS NIH HHS R01 GM097158NIGMS NIH HHS R01GM097158
6 · The paper itself

Abstract

Epithelial stem cells are routinely lost or damaged during adult life and must therefore be replaced to maintain homeostasis. Recent studies indicate that stem cell replacement occurs through neutral competition in many types of epithelial tissues, but little is known about the factors that determine competitive outcome. The epithelial follicle stem cells (FSCs) in the Drosophila ovary are regularly lost and replaced during normal homeostasis, and we show that FSC replacement conforms to a model of neutral competition. In addition, we found that FSCs mutant for the basolateral junction genes, lethal giant larvae (lgl) or discs large (dlg), undergo a biased competition for niche occupancy characterized by increased invasion of neighboring FSCs and reduced loss. Interestingly, FSCs mutant for a third basolateral junction gene, scribble (scrib), do not exhibit biased competition, suggesting that Lgl and Dlg regulate niche competition through a Scrib-independent process. Lastly, we found that FSCs have a unique cell polarity characterized by broadly distributed adherens junctions and the lack of a mature apical domain. Collectively, these observations indicate that Lgl and Dlg promote the differentiation of FSC progeny to a state in which they are less prone to invade the neighboring niche. In addition, we demonstrate that the neutral drift model can be adapted to quantify non-neutral behavior of mutant clones.

Indexed as

Stem Cell NicheAdult Stem CellsAnimalsCell DifferentiationCell PolarityDrosophilaDrosophila ProteinsFemaleMutationNerve Growth FactorsOvarian FollicleTumor Suppressor Proteinsdlg1 protein, DrosophilaDrosophila Proteinsl(2)gl protein, DrosophilaNerve Growth Factorssbb protein, DrosophilaTumor Suppressor Proteins

Identifiers

PMID24991805
PMCPMC4084627
OpenAlexW2059599142

What OpenQuestion holds

Textmetadata
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.