The epigenetic regulation of synaptic genes contributes to the etiology of autism

Rev Neurosci. 2021 May 4;32(7):791-802. doi: 10.1515/revneuro-2021-0014. Print 2021 Nov 25.

Abstract

Epigenetic mechanisms greatly affect the developing brain, as well as the maturation of synapses with pervasive, long-lasting consequences on behavior in adults. Substantial evidence exists that implicates dysregulation of epigenetic mechanisms in the etiology of neurodevelopmental disorders. Therefore, this review explains the role of enzymes involved in DNA methylation and demethylation in neurodevelopment by emphasizing changes of synaptic genes and proteins. Epigenetic causes of sex-dependent differences in the brain are analyzed in conjunction with the pathophysiology of autism spectrum disorders. Special attention is devoted to the epigenetic regulation of the melanoma-associated antigen-like gene 2 (MAGEL2) found in Prader-Willi syndrome, which is known to be accompanied by autistic symptoms.

Keywords: autism; epigenetic mechanisms; methylation; synaptic proteins.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Autism Spectrum Disorder* / genetics
  • Autistic Disorder* / genetics
  • Brain
  • DNA Methylation / genetics
  • Epigenesis, Genetic
  • Humans
  • Proteins

Substances

  • MAGEL2 protein, human
  • Proteins