Evidence map›Paper›PMID 29093440›Full record

ArticleNature communications2017

Quantitative microscopy of the Drosophila ovary shows multiple niche signals specify progenitor cell fate.

Wei Dai, Amy Peterson, Thomas Kenney, Haley Burrous, Denise J Montell

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  5. Starve-Feed Cycles Direct Quiescence to Proliferation Transitions inbioRxiv : the preprint server for biology · 2026
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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

5 authors at 1 institution in 1 country.

Wei DaiMCDB Department, University of California, Santa Barbara, CA, 93106, USA.
Amy PetersonMCDB Department, University of California, Santa Barbara, CA, 93106, USA.
Thomas KenneyMCDB Department, University of California, Santa Barbara, CA, 93106, USA.
Haley BurrousMCDB Department, University of California, Santa Barbara, CA, 93106, USA.
Denise J MontellMCDB Department, University of California, Santa Barbara, CA, 93106, USA. denise.montell@lifesci.ucsb.edu.ORCID http://orcid.org/0000-0001-8924-5925
University of California, Santa Barbara · US

Funding

Spatiotemporal regulation of collective cell behaviors in Drosophila: Diversity Supplement for Predoctoral TrainingR01GM046425 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MONTELL, DENISE J. · 1996 to 2025
$11.7M
Spectral Laser Scanning Biological MicroscopeS10OD010610 · OD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI RAVEN, MARY A · 2012 to 2012
$429k
NIGMS NIH HHS R01 GM046425NIH HHS S10 OD010610
6 · The paper itself

Abstract

Adult stem cells commonly give rise to transit-amplifying progenitors, whose progeny differentiate into distinct cell types. It is unclear if stem cell niche signals coordinate fate decisions within the progenitor pool. Here we use quantitative analysis of Wnt, Hh, and Notch signalling reporters and the cell fate markers Eyes Absent (Eya) and Castor (Cas) to study the effects of hyper-activation and loss of niche signals on progenitor development in the Drosophila ovary. Follicle stem cell (FSC) progeny adopt distinct polar, stalk, and main body cell fates. We show that Wnt signalling transiently inhibits expression of the main body cell fate determinant Eya, and Wnt hyperactivity strongly biases cells towards polar and stalk fates. Hh signalling independently controls the proliferation to differentiation transition. Notch is permissive but not instructive for differentiation of multiple cell types. These findings reveal that multiple niche signals coordinate cell fates and differentiation of progenitor cells.

Indexed as

Stem Cell NicheAdult Stem CellsAnimalsCell DifferentiationDNA-Binding ProteinsDrosophilaDrosophila ProteinsEye ProteinsFemaleHedgehog ProteinsMicroscopyOvarian FollicleOvaryReceptors, NotchWnt ProteinsWnt Signaling Pathwaycas protein, DrosophilaDNA-Binding ProteinsDrosophila Proteinseya protein, DrosophilaEye ProteinsHedgehog Proteinshh protein, DrosophilaN protein, DrosophilaReceptors, NotchWnt Proteins

Identifiers

PMID29093440
PMCPMC5665863
OpenAlexW2766754462

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.