Evidence map›Paper›PMID 27705795›Full record

ArticleCell reports2016

MyT1 Counteracts the Neural Progenitor Program to Promote Vertebrate Neurogenesis.

Francisca F Vasconcelos, Alessandro Sessa, Cátia Laranjeira, Alexandre A S F Raposo, Vera Teixeira, Daniel W Hagey, Diogo M Tomaz, Jonas Muhr, Vania Broccoli, Diogo S Castro

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Stimulus-Dependent Expression ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  9. Asynchronous microexon splicing ofbioRxiv : the preprint server for biology · 2024
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  16. ESC-sEVs Rejuvenate Aging Hippocampal NSCs by Transferring SMADs to Regulate the MYT1-Egln3-Sirt1 Axis.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  17. Article
  18. MYT1 role in the microtia-craniofacial microsomia spectrum.Molecular genetics & genomic medicine · 2020
    Article
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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

10 authors at 3 institutions in 3 countries.

Francisca F VasconcelosInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Alessandro SessaDivision of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy.
Cátia LaranjeiraInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Alexandre A S F RaposoInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Vera TeixeiraInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Daniel W HageyDepartment of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden.
Diogo M TomazInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Jonas MuhrDepartment of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden.
Vania BroccoliDivision of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy.
Diogo S CastroInstituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal. Electronic address: dscastro@igc.gulbenkian.pt.
Instituto Gulbenkian de Ciência · PTLudwig Cancer Research · SESan Raffaele University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1, Sox2, Id3, and Olig1. Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationDNA-Binding ProteinsGene Expression Regulation, DevelopmentalInhibitor of Differentiation ProteinsMiceNeural Stem CellsNeurogenesisNeuronsReceptor, Notch1SOXB1 Transcription FactorsStem CellsTranscription Factor HES-1Transcription FactorsVertebratesAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsHes1 protein, mouseIdb3 protein, mouseInhibitor of Differentiation ProteinsMyt1 protein, mouseNotch1 protein, mouseOlig1 protein, mouseReceptor, Notch1Sox2 protein, mouseSOXB1 Transcription FactorsTranscription Factor HES-1Transcription FactorsAscl1Hes1MyT1neurogenesisNotch signalingRbpjtranscription

Identifiers

PMID27705795
PMCPMC5067283
OpenAlexW2529622579

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.