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Impact of KDM6B mosaic brain knockout on synaptic function and behavior.
- Source :
-
Scientific reports [Sci Rep] 2024 Sep 02; Vol. 14 (1), pp. 20416. Date of Electronic Publication: 2024 Sep 02. - Publication Year :
- 2024
-
Abstract
- Autism spectrum disorders (ASD) are complex neurodevelopmental conditions characterized by impairments in social communication, repetitive behaviors, and restricted interests. Epigenetic modifications serve as critical regulators of gene expression playing a crucial role in controlling brain function and behavior. Lysine (K)-specific demethylase 6B (KDM6B), a stress-inducible H3K27me3 demethylase, has emerged as one of the highest ASD risk genes, but the precise effects of KDM6B mutations on neuronal activity and behavioral function remain elusive. Here we show the impact of KDM6B mosaic brain knockout on the manifestation of different autistic-like phenotypes including repetitive behaviors, social interaction, and significant cognitive deficits. Moreover, KDM6B mosaic knockout display abnormalities in hippocampal excitatory synaptic transmission decreasing NMDA receptor mediated synaptic transmission and plasticity. Understanding the intricate interplay between epigenetic modifications and neuronal function may provide novel insights into the pathophysiology of ASD and potentially inform the development of targeted therapeutic interventions.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Mice
Brain metabolism
Neuronal Plasticity genetics
Behavior, Animal
Hippocampus metabolism
Epigenesis, Genetic
Male
Synapses metabolism
Jumonji Domain-Containing Histone Demethylases genetics
Jumonji Domain-Containing Histone Demethylases metabolism
Mice, Knockout
Synaptic Transmission genetics
Autism Spectrum Disorder genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 14
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 39223259
- Full Text :
- https://doi.org/10.1038/s41598-024-70728-5