A mouse model of ATRX deficiency with cognitive deficits and autistic traits

J Neurodev Disord. 2023 Nov 13;15(1):39. doi: 10.1186/s11689-023-09508-7.

Abstract

Background: ATRX is an ATP-dependent chromatin remodeling protein with essential roles in safeguarding genome integrity and modulating gene expression. Deficiencies in this protein cause ATR-X syndrome, a condition characterized by intellectual disability and an array of developmental abnormalities, including features of autism. Previous studies demonstrated that deleting ATRX in mouse forebrain excitatory neurons postnatally resulted in male-specific memory deficits, but no apparent autistic-like behaviours.

Methods: We generated mice with an earlier embryonic deletion of ATRX in forebrain excitatory neurons and characterized their behaviour using a series of memory and autistic-related paradigms.

Results: We found that mutant mice displayed a broader spectrum of impairments, including fear memory, decreased anxiety-like behaviour, hyperactivity, as well as self-injurious and repetitive grooming. Sex-specific alterations were also observed, including male-specific aggression, sensory gating impairments, and decreased social memory.

Conclusions: Collectively, the findings indicate that early developmental abnormalities arising from ATRX deficiency in forebrain excitatory neurons contribute to the presentation of fear memory deficits as well as autistic-like behaviours.

Keywords: ATRX; Autism; Intellectual disability; Mice; Sex differences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autistic Disorder* / complications
  • Autistic Disorder* / genetics
  • Cognition
  • Female
  • Male
  • Memory Disorders / etiology
  • Mice
  • Neurons / physiology

Supplementary concepts

  • ATR-X syndrome