Evidence map›Paper›PMID 26092848›Full record

ArticleDevelopment (Cambridge, England)2015

Traffic jam functions in a branched pathway from Notch activation to niche cell fate.

Lindsey Wingert, Stephen DiNardo

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Lin28 Represses Hub Cell microRNAs to MaintainDevelopment & reproduction · 2026
    Review
  2. Article
  3. Article
  4. Notch signaling sculpts the stem cell niche.Frontiers in cell and developmental biology · 2022
    Review
  5. 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

2 authors.

Lindsey WingertDepartment of Cell & Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Stephen DiNardoDepartment of Cell & Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA sdinardo@mail.med.upenn.edu.

Funding

Stem Cell Renewal And Differentiation in SpermatogenesisR01GM060804 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DINARDO, STEPHEN FRANCIS · 1999 to 2019
$6.7M
TRAINING PROGRAM IN DEVELOPMENTAL BIOLOGYT32HD007516 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI RAPER, JONATHAN A · 1998 to 2012
$5.6M
NICHD NIH HHS T32 HD007516NICHD NIH HHS T32HD007516NIGMS NIH HHS R01 GM060804NIGMS NIH HHS R01 GM60804
6 · The paper itself

Abstract

The niche directs key behaviors of its resident stem cells, and is thus crucial for tissue maintenance, repair and longevity. However, little is known about the genetic pathways that guide niche specification and development. The male germline stem cell niche in Drosophila houses two stem cell populations and is specified within the embryonic gonad, thus making it an excellent model for studying niche development. The hub cells that form the niche are specified early by Notch activation. Over the next few hours, these individual cells then cluster together and take up a defined position before expressing markers of hub cell differentiation. This timing suggests that there are other factors for niche development yet to be defined. Here, we have identified a role for the large Maf transcription factor Traffic jam (Tj) in hub cell specification downstream of Notch. Tj downregulation is the first detectable effect of Notch activation in hub cells. Furthermore, Tj depletion is sufficient to generate ectopic hub cells that can recruit stem cells. Surprisingly, ectopic niche cells in tj mutants remain dispersed in the absence of Notch activation. This led us to uncover a branched pathway downstream of Notch in which Bowl functions to direct hub cell assembly in parallel to Tj downregulation.

Indexed as

Cell LineageStem Cell NicheAnimalsCell DifferentiationDown-RegulationDrosophila melanogasterDrosophila ProteinsGerm CellsGonadsMaf Transcription Factors, LargeMaleModels, BiologicalMutationProto-Oncogene ProteinsReceptors, NotchSignal TransductionDrosophila ProteinsMaf Transcription Factors, LargeN protein, DrosophilaProto-Oncogene ProteinsReceptors, Notchtj protein, DrosophilaDrosophilaGonadogenesisNotchStem cell nicheTraffic jam

Identifiers

PMID26092848
PMCPMC4510594

What OpenQuestion holds

Textmetadata
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.