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• W3037263485 abstract "Abstract Background Alpha-thalassemia/mental retardation, X-linked, or ATRX , is an autism susceptibility gene that encodes a chromatin remodeler. Mutations of ATRX result in the ATR-X intellectual disability syndrome and have been identified in autism spectrum disorder (ASD) patients. The mechanisms by which ATRX mutations lead to autism and autistic-like behaviours are not yet known. To address this question, we generated mice with postnatal Atrx inactivation in excitatory neurons of the forebrain and performed a battery of behavioural assays that assess autistic-like behaviours. Methods Male and female mice with a postnatal conditional ablation of ATRX were generated using the Cre/lox system under the control of the αCaMKII gene promoter. These mice were tested in a battery of behavioural tests that assess autistic-like features. We utilized paradigms that measure social behaviour, repetitive, and stereotyped behaviours, as well as sensory gating. Statistics were calculated by two-way repeated measures ANOVA with Sidak’s multiple comparison test or unpaired Student’s t tests as indicated. Results The behaviour tests revealed no significant differences between Atrx -cKO and control mice. We identified sexually dimorphic changes in odor habituation and discrimination; however, these changes did not correlate with social deficits. Conclusion The postnatal knockout of Atrx in forebrain excitatory neurons does not lead to autism-related behaviours in male or female mice." @default.
• W3037263485 created "2020-07-02" @default.
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• W3037263485 date "2020-06-24" @default.
• W3037263485 modified "2023-10-17" @default.
• W3037263485 title "Effects of a postnatal Atrx conditional knockout in neurons on autism-like behaviours in male and female mice" @default.
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• W3037263485 doi "https://doi.org/10.1186/s11689-020-09319-0" @default.
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