Connecting Genotype with Behavioral Phenotype in Mouse Models of Autism Associated with PTEN Mutations

Cold Spring Harb Perspect Med. 2020 Sep 1;10(9):a037010. doi: 10.1101/cshperspect.a037010.

Abstract

A subset of individuals with autism spectrum disorder (ASD) and macrocephaly carry mutations in the gene PTEN. Animal models, particularly mice, have been helpful in establishing a causal role for Pten mutations in autism-relevant behavioral deficits. These models are a useful tool for investigating neurobiological mechanisms of these behavioral phenotypes and developing potential therapeutic interventions. Here we provide an overview of various genetic mouse models that have been used to characterize behavioral phenotypes caused by perturbation of Pten We discuss convergent and divergent phenotypes across models with the aim of highlighting a set of behavioral domains that are sensitive to the effects of Pten mutation and that may provide useful readouts for translational and basic neuroscience research.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Autism Spectrum Disorder / genetics*
  • Behavior*
  • Disease Models, Animal
  • Genotype
  • Humans
  • Megalencephaly / genetics
  • Mice
  • Mutation
  • PTEN Phosphohydrolase / genetics*
  • Phenotype

Substances

  • PTEN Phosphohydrolase
  • PTEN protein, human