Evidence map›Paper›PMID 40187474›Full record

ArticleDevelopmental biology2025

ASCL1 protein domains with distinct functions in neuronal differentiation and subtype specification.

Yuji Nakada, Madison J Martinez, Jane E Johnson

Abstract read
In one paragraph

Article in Developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

3 authors.

Yuji NakadaDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, TX, 75390, USA. Electronic address: nkdyuji@uab.edu.
Madison J MartinezDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, TX, 75390, USA.
Jane E JohnsonDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX, 75390, USA. Electronic address: jane.johnson@utsouthwestern.edu.

Funding

REGULATION OF THE NEURAL DETERMINATION GENE MASH1R01NS032817 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI JOHNSON, JANE E · 1995 to 2016
$5.8M
BHLH TRANSCRIPTION FACTORS IN NEURAL DEVELOPMENTR01HD037932 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI JOHNSON, JANE E · 2000 to 2015
$4.9M
Transcription Factor Control of Neuronal DiversityR37HD091856 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI Jane E Johnson · 2017 to 2026
$4.7M
NICHD NIH HHS R01 HD037932NICHD NIH HHS R37 HD091856NINDS NIH HHS R01 NS032817
6 · The paper itself

Abstract

ASCL1 is a neural basic helix-loop-helix (bHLH) transcription factor that plays essential roles during neural development, including neural differentiation and neuronal subtype specification. bHLH factors are defined by their motifs, including a basic region interacting with DNA and an HLH domain involved in protein-protein interactions. We previously defined specific regions within the bHLH domain of ASCL1 as important for its specific functions directing neuronal differentiation in the chick neural tube. Here, we build upon these findings to show how specific mutations within the basic region block DNA binding but not heterodimer formation with E-protein partners TCF3 (E12/E47) and TCF12 (HEB) yet have differential abilities to show dominant negative phenotypes. Additionally, truncating domains outside the bHLH define a nuclear localization signal, a requirement for the C-terminal acidic residues, and the non-essentiality of the N-terminal glutamine/alanine repeats. This structure/function analysis identifies functional domains for ASCL1 activity.

Indexed as

Basic Helix-Loop-Helix ProteinsCell DifferentiationNeurogenesisNeuronsAnimalsChick EmbryoMutationNeural TubeProtein DomainsBasic Helix-Loop-Helix ProteinsASCL1bHLH transcription factorsNeurogenesisNeuronal specificationSpinal cord development

Identifiers

PMID40187474
PMCPMC12535295

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Registered trials

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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.