Evidence map›Paper›PMID 33241994›Full record

ArticleeLife2020

Sequential activation of transcriptional repressors promotes progenitor commitment by silencing stem cell identity genes.

Noemi Rives-Quinto, Hideyuki Komori, Cyrina M Ostgaard, Derek H Janssens, Shu Kondo, Qi Dai, Adrian W Moore, Cheng-Yu Lee

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Altering cell size asymmetry inbioRxiv : the preprint server for biology · 2025
    Article
  5. eLife · 2025
    Article
  6. Article
  7. Article
  8. Brain development and bioenergetic changes.Neurobiology of disease · 2024
    Review
  9. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

8 authors at 4 institutions in 3 countries.

Noemi Rives-QuintoLife Sciences Institute, University of Michigan, Ann Arbor, United States.
Hideyuki KomoriLife Sciences Institute, University of Michigan, Ann Arbor, United States.ORCID 0000-0001-9764-5654
Cyrina M OstgaardLife Sciences Institute, University of Michigan, Ann Arbor, United States.
Derek H JanssensLife Sciences Institute, University of Michigan, Ann Arbor, United States.
Shu KondoInvertebrate Genetics Laboratory, National Institute of Genetics, Mishima, Japan.ORCID 0000-0002-4625-8379
Qi DaiDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.
Adrian W MooreRiken Center for Brain Science, Wako, Japan.
Cheng-Yu LeeLife Sciences Institute, University of Michigan, Ann Arbor, United States.ORCID 0000-0003-2291-1297
University of Michigan · USNational Institute of Genetics · JPRIKEN Center for Brain Science · JPStockholm University · SE

Funding

Shared mechanisms regulate transcription-factor activity to control cell fate in neural stem cells and the embryoR01NS111647 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI HARRISON, MELISSA, LEE, CHENG-YU · 2019 to 2023
$1.7M
Multi-layered Control of the Exit from StemnessR01NS107496 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, CHENG-YU · 2019 to 2023
$1.7M
NINDS NIH HHS R01 NS107496NINDS NIH HHS R01 NS111647
6 · The paper itself

Abstract

Stem cells that indirectly generate differentiated cells through intermediate progenitors drives vertebrate brain evolution. Due to a lack of lineage information, how stem cell functionality, including the competency to generate intermediate progenitors, becomes extinguished during progenitor commitment remains unclear. Type II neuroblasts in fly larval brains divide asymmetrically to generate a neuroblast and a progeny that commits to an intermediate progenitor (INP) identity. We identified Tailless (Tll) as a master regulator of type II neuroblast functional identity, including the competency to generate INPs. Successive expression of transcriptional repressors functions through Hdac3 to silence

Indexed as

Gene SilencingNeurogenesisTranscriptional ActivationAnimalsAnimals, Genetically ModifiedBrainCell LineageDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalHistone DeacetylasesLarvaNeural Stem CellsPhenotypeReceptors, NotchRepressor ProteinsDrosophila ProteinsHdac3 protein, DrosophilaHistone DeacetylasesN protein, DrosophilaReceptors, NotchRepressor ProteinsTLL protein, DrosophilaTranscription FactorsD. melanogasterintermediate progenitorsneural stem cellsneuroblastneurogenesisNotch signalingregenerative medicinestem cells

Identifiers

PMID33241994
PMCPMC7728440
OpenAlexW3110265605

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.