Evidence map›Paper›PMID 42118999›Full record

ArticleGenetics2026

Regulation of somatic stem cell development through positional and proliferative signals during Drosophila melanogaster pupal ovary development resembles the framework governing adult stem cell behavior.

Rachel Misner, Amy Reilein, Helen V Kogan, Daniel Kalderon

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rachel MisnerDepartment of Biological Sciences, Columbia University, 1212 Amsterdam Avenue, NewYork, NY 10027, United States.
Amy ReileinDepartment of Biological Sciences, Columbia University, 1212 Amsterdam Avenue, NewYork, NY 10027, United States.
Helen V KoganDepartment of Biological Sciences, Columbia University, 1212 Amsterdam Avenue, NewYork, NY 10027, United States.
Daniel KalderonDepartment of Biological Sciences, Columbia University, 1212 Amsterdam Avenue, NewYork, NY 10027, United States.ORCID 0000-0002-2149-0673

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
NIH HHS P40 OD018537NIH HHS RO1 GM079351
6 · The paper itself

Abstract

Follicle stem cells (FSCs) in the Drosophila melanogaster ovary are maintained through independent regulation of division and differentiation to become proliferative follicle cells (FCs) to their posterior or quiescent escort cells (ECs) to their anterior. These behaviors are guided by graded extracellular Hedgehog (Hh) and Wnt signals emanating from cells anterior to FSCs and an inverse gradient of JAK-STAT pathway activity. Here, we used lineage analyses to investigate regulation of the development of ECs, FSCs, and FCs from a common set of precursors during pupation. Previous studies found that the most anterior precursors divide slowest, with quiescence spreading from the anterior over time to include all ECs, that FSCs are specified simply by their location at eclosion, and that the first FCs derive from cells that accumulate posterior to the developing germline over the first 48 h of pupation. We found that Wnt pathway activity favored conversion of precursors to more anterior adult derivatives (ECs rather than FCs), while JAK-STAT pathway activity favored posterior outcomes. Faster division, explored by altering Cyclin E activity, favored a precursor becoming an FSC. Both JAK-STAT and Hh signaling could increase precursor division rate. All of these characteristics resemble regulation of adult FSC behavior. We suggest that the regulation of both stem cell specification and maintenance by a similar set of extracellular signals, by directly influencing cell location and cell division rate, may be general features for stem cells that are specified in parallel with tissue development and that exhibit division-independent differentiation.

Indexed as

Adult Stem CellsDrosophila melanogasterOvaryStem CellsAnimalsCell DifferentiationCell LineageCell ProliferationCyclin EDrosophila ProteinsFemaleHedgehog ProteinsJanus KinasesOvarian FolliclePupaSignal TransductionCyclin EDrosophila ProteinsHedgehog ProteinsJanus KinasesSTAT Transcription Factors

Identifiers

PMID42118999
PMCPMC13291918

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.