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

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:EMBO reports 2021-06, Vol.22 (6), p.e50958-n/a
Hauptverfasser: Jamadagni, Priyanka, Breuer, Maximilian, Schmeisser, Kathrin, Cardinal, Tatiana, Kassa, Betelhem, Parker, J Alex, Pilon, Nicolas, Samarut, Eric, Patten, Shunmoogum A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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 −/− model. chd7 −/− mutants have less GABAergic neurons and exhibit a hyperactivity behavioural phenotype. The GABAergic neuron defect is at least in part due to downregulation of the CHD7 direct target gene paqr3b , and subsequent upregulation of MAPK/ERK signalling, which is also dysregulated in CHD7 mutant human cells. Through a phenotype-based screen in chd7 −/− zebrafish and Caenorhabditis elegans , we show that the small molecule ephedrine restores normal levels of MAPK/ERK signalling and improves both GABAergic defects and behavioural anomalies. We conclude that chd7 promotes paqr3b expression and that this is required for normal GABAergic network development. This work provides insight into the neuropathogenesis associated with CHD7 deficiency and identifies a promising compound for further preclinical studies. SYNOPSIS Loss-of-function of chd7 causes defects in GABAergic neuron development and behavioural anomalies reminiscent of CHARGE syndrome, which are rescued by genetic and pharmacological interventions in zebrafish. Zebrafish chd7 −/− larvae display aberrant GABAergic network development and hyperactivity behavioral phenotypes. Downregulation of paqr3b expression contributes to the GABAergic neuron defects in zebrafish chd7 −/− larval brains. Ephedrine rescues the GABAergic neuron and behavioral defects. Graphical Abstract Loss-of-function of chd7 causes defects in GABAergic neuron development and behavioural anomalies reminiscent of CHARGE syndrome, which are rescued by genetic and pharmacological interventions in zebrafish.
ISSN:1469-221X
1469-3178
DOI:10.15252/embr.202050958