Evidence map›Paper›PMID 8816493›Full record

ArticleMolecular and cellular biology1996

NeuroD2 and neuroD3: distinct expression patterns and transcriptional activation potentials within the neuroD gene family.

M B McCormick, R M Tamimi, L Snider, A Asakura, D Bergstrom, S J Tapscott

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
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  8. T-cell TGF-β signaling abrogation restricts medulloblastoma progression.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  9. Skeletal muscle programming and re-programming.Current opinion in genetics & development · 2013
    Review
  10. NeuroD modulates opioid agonist-selective regulation of adult neurogenesis and contextual memory extinction.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Article
  11. Article
  12. Article
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  15. Transcriptional regulatory regions of gap43 needed in developing and regenerating retinal ganglion cells.Developmental dynamics : an official publication of the American Association of Anatomists · 2010
    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

6 authors at 2 institutions in 1 country.

M B McCormickFred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.
R M Tamimi
L Snider
A Asakura
D Bergstrom
S J Tapscott
Fred Hutch Cancer Center · USUniversity of Washington Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have identified two new genes, neuroD2 and neuroD3, on the basis of their similarity to the neurogenic basic-helix-loop-helix (bHLH) gene neuroD. The predicted amino acid sequence of neuroD2 shows a high degree of homology to neuroD and MATH-2/NEX-1 in the bHLH region, whereas neuroD3 is a more distantly related family member. neuroD3 is expressed transiently during embryonic development, with the highest levels of expression between days 10 and 12. neuroD2 is initially expressed at embryonic day 11, with persistent expression in the adult nervous system. In situ and Northern (RNA) analyses demonstrate that different regions of the adult nervous system have different relative amounts of neuroD and neuroD2 RNA. Similar to neuroD, expression of neuroD2 in developing Xenopus laevis embryos results in ectopic neurogenesis, indicating that neuroD2 mediates neuronal differentiation. Transfection of vectors expressing neuroD and neuroD2 into P19 cells shows that both can activate expression through simple E-box-driven reporter constructs and can activate a reporter driven by the neuroD2 promoter region, but the GAP-43 promoter is preferentially activated by neuroD2. The noncongruent expression pattern and target gene specificity of these highly related neurogenic bHLH proteins make them candidates for conferring specific aspects of the neuronal phenotype.

Indexed as

Gene Expression Regulation, DevelopmentalMultigene FamilyTranscriptional ActivationAdultAmino Acid SequenceAnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsBrainCell LineDrosophila melanogasterEmbryo, MammalianEmbryonic and Fetal DevelopmentEmbryo, NonmammalianFetusFibroblastsBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNEUROD2 protein, humanNeurod2 protein, mouseNEUROG1 protein, humanNeurog1 protein, mouseNeurogenic differentiation factor 1NeuropeptidesRecombinant ProteinsTranscription Factors

Identifiers

PMID8816493
PMCPMC231580
OpenAlexW2123164631

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.