Evidence map›Paper›PMID 24643195›Full record

ArticlePloS one2014

Ascl1 as a novel player in the Ptf1a transcriptional network for GABAergic cell specification in the retina.

Nicolas Mazurier, Karine Parain, Damien Parlier, Silvia Pretto, Johanna Hamdache, Philippe Vernier, Morgane Locker, Eric Bellefroid, Muriel Perron

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Development of the Vertebrate Eye and Retina.Progress in molecular biology and translational science · 2015
    Review
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

9 authors at 2 institutions in 1 country.

Nicolas MazurierUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Karine ParainUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Damien ParlierULB-IBMM, Laboratoire d'Embryologie Moléculaire, Gosselies, Belgium.
Silvia PrettoUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Johanna HamdacheUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Philippe VernierUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, Institut A. Fessard, Gif-Sur-Yvette, France.
Morgane LockerUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Eric BellefroidULB-IBMM, Laboratoire d'Embryologie Moléculaire, Gosselies, Belgium.
Muriel PerronUPR Centre national de la recherche scientifique 3294 Neurobiology and Development, University Paris Sud, Orsay, France.
Laboratoire de Neurobiologie Cellulaire et Moléculaire · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In contrast with the wealth of data involving bHLH and homeodomain transcription factors in retinal cell type determination, the molecular bases underlying neurotransmitter subtype specification is far less understood. Using both gain and loss of function analyses in Xenopus, we investigated the putative implication of the bHLH factor Ascl1 in this process. We found that in addition to its previously characterized proneural function, Ascl1 also contributes to the specification of the GABAergic phenotype. We showed that it is necessary for retinal GABAergic cell genesis and sufficient in overexpression experiments to bias a subset of retinal precursor cells towards a GABAergic fate. We also analysed the relationships between Ascl1 and a set of other bHLH factors using an in vivo ectopic neurogenic assay. We demonstrated that Ascl1 has unique features as a GABAergic inducer and is epistatic over factors endowed with glutamatergic potentialities such as Neurog2, NeuroD1 or Atoh7. This functional specificity is conferred by the basic DNA binding domain of Ascl1 and involves a specific genetic network, distinct from that underlying its previously demonstrated effects on catecholaminergic differentiation. Our data show that GABAergic inducing activity of Ascl1 requires the direct transcriptional regulation of Ptf1a, providing therefore a new piece of the network governing neurotransmitter subtype specification during retinogenesis.

Indexed as

Transcription, GeneticAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationEmbryo, Nonmammaliangamma-Aminobutyric AcidGene Expression Regulation, DevelopmentalGene Regulatory NetworksNerve Tissue ProteinsNeuronsReceptors, GABARetinaSignal TransductionXenopus laevisXenopus Proteinsascl1 protein, XenopusBasic Helix-Loop-Helix Proteinsgamma-Aminobutyric AcidNerve Tissue ProteinsPtf1a protein, XenopusReceptors, GABAXenopus Proteins

Identifiers

PMID24643195
PMCPMC3958475
OpenAlexW2078934457

What OpenQuestion holds

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LicenceCC BY
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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.