Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression.


Journal

EMBO reports
ISSN: 1469-3178
Titre abrégé: EMBO Rep
Pays: England
ID NLM: 100963049

Informations de publication

Date de publication:
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

e50958

Subventions

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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Auteurs

Priyanka Jamadagni (P)

INRS- Centre Armand-Frappier Santé Biotechnologie, Laval, QC, Canada.

Maximilian Breuer (M)

INRS- Centre Armand-Frappier Santé Biotechnologie, Laval, QC, Canada.

Kathrin Schmeisser (K)

Centre de recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC, Canada.

Tatiana Cardinal (T)

Centre d'Excellence en Recherche sur les Maladies Orphelines - Fondation Courtois (CERMO-FC), Université du Québec à Montréal (UQAM), Montréal, QC, Canada.

Betelhem Kassa (B)

INRS- Centre Armand-Frappier Santé Biotechnologie, Laval, QC, Canada.

J Alex Parker (JA)

Centre de recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC, Canada.
Modelis inc., Montréal, QC, Canada.

Nicolas Pilon (N)

Centre d'Excellence en Recherche sur les Maladies Orphelines - Fondation Courtois (CERMO-FC), Université du Québec à Montréal (UQAM), Montréal, QC, Canada.
Département des sciences biologiques, Université du Québec à Montréal (UQAM), Montréal, QC, Canada.
Département de pédiatrie, Université de Montréal, Montréal, QC, Canada.

Eric Samarut (E)

Centre de recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC, Canada.
Modelis inc., Montréal, QC, Canada.

Shunmoogum A Patten (SA)

INRS- Centre Armand-Frappier Santé Biotechnologie, Laval, QC, Canada.
Centre d'Excellence en Recherche sur les Maladies Orphelines - Fondation Courtois (CERMO-FC), Université du Québec à Montréal (UQAM), Montréal, QC, Canada.

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Classifications MeSH