Evidence map›Paper›PMID 35020878›Full record

ArticleDevelopment (Cambridge, England)2021

Distinct roles of Bendless in regulating FSC niche competition and daughter cell differentiation.

Sumitra Tatapudy, Jobelle Peralta, Todd Nystul

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

3 authors.

Sumitra TatapudyDepartment of Anatomy and Department of OB/Gyn-RS, University of California, San Francisco, Center for Reproductive Sciences, Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, 513 Parnassus Avenue, San Francisco, CA, 94143, USA.ORCID 0000-0002-7604-1138
Jobelle PeraltaDepartment of Anatomy and Department of OB/Gyn-RS, University of California, San Francisco, Center for Reproductive Sciences, Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, 513 Parnassus Avenue, San Francisco, CA, 94143, USA.ORCID 0000-0002-9442-1257
Todd NystulDepartment of Anatomy and Department of OB/Gyn-RS, University of California, San Francisco, Center for Reproductive Sciences, Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, 513 Parnassus Avenue, San Francisco, CA, 94143, USA.ORCID 0000-0002-6250-2394

Funding

Cell Fate Decisions in Epithelial Stem Cell LineagesR35GM136348 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 2020 to 2026
$3.9M
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
NIGMS NIH HHS R01 GM097158NIGMS NIH HHS R35 GM136348
6 · The paper itself

Abstract

A major goal in the study of adult stem cells is to understand how cell fates are specified at the proper time and place to facilitate tissue homeostasis. Here, we found that an E2 ubiquitin ligase, Bendless (Ben), has multiple roles in the Drosophila ovarian epithelial follicle stem cell (FSC) lineage. First, Ben is part of the JNK signaling pathway, and we found that it, as well as other JNK pathway genes, are essential for differentiation of FSC daughter cells. Our data suggest that JNK signaling promotes differentiation by suppressing the activation of the EGFR effector, ERK. Also, we found that loss of ben, but not the JNK kinase hemipterous, resulted in an upregulation of hedgehog signaling, increased proliferation and increased niche competition. Lastly, we demonstrate that the hypercompetition phenotype caused by loss of ben is suppressed by decreasing the rate of proliferation or knockdown of the hedgehog pathway effector, Smoothened (Smo). Taken together, our findings reveal a new layer of regulation in which a single gene influences cell signaling at multiple stages of differentiation in the early FSC lineage.

Indexed as

AnimalsCell DifferentiationCell LineageCell ProliferationDrosophila melanogasterDrosophila ProteinsEpithelial CellsErbB ReceptorsFemaleHedgehog ProteinsMAP Kinase Signaling SystemOvarian FollicleReceptors, Invertebrate PeptideSmoothened ReceptorStem Cell NicheStem Cellsben protein, DrosophilaDrosophila ProteinsEgfr protein, DrosophilaErbB ReceptorsHedgehog Proteinshh protein, DrosophilaReceptors, Invertebrate PeptideSmoothened Receptorsmo protein, DrosophilaUbiquitin-Conjugating EnzymesDrosophilaEpithelial stem cellFollicle epitheliumHedgehogJNKNotch

Identifiers

PMID35020878
PMCPMC8645206

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.