Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression.
CHD7
GABA
behaviour
neurodevelopment
zebrafish
Journal
EMBO reports
ISSN: 1469-3178
Titre abrégé: EMBO Rep
Pays: England
ID NLM: 100963049
Informations de publication
Date de publication:
04 06 2021
04 06 2021
Historique:
revised:
07
03
2021
received:
25
05
2020
accepted:
15
03
2021
pubmed:
27
4
2021
medline:
29
6
2021
entrez:
26
4
2021
Statut:
ppublish
Résumé
Mutations in the chromatin remodeller-coding gene CHD7 cause CHARGE syndrome (CS). CS features include moderate to severe neurological and behavioural problems, clinically characterized by intellectual disability, attention-deficit/hyperactivity disorder and autism spectrum disorder. To investigate the poorly characterized neurobiological role of CHD7, we here generate a zebrafish chd7
Identifiants
pubmed: 33900016
doi: 10.15252/embr.202050958
pmc: PMC8183419
doi:
Substances chimiques
Chromatin
0
DNA-Binding Proteins
0
Intracellular Signaling Peptides and Proteins
0
Membrane Proteins
0
PAQR3 protein, human
0
DNA Helicases
EC 3.6.4.-
CHD7 protein, human
EC 3.6.4.12
Banques de données
GEO
['GSE139623']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e50958Subventions
Organisme : CHARGE Syndrome Foundation
Organisme : Canada Foundation for Innovation (CFI)
Organisme : Rare Disease Foundation (RDF)
Organisme : Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (NSERC)
Organisme : Fonds de Recherche du Québec - Santé (FRQS)
Organisme : CIHR
Pays : Canada
Informations de copyright
© 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license.
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