Decreased aggression and increased repetitive behavior in Pten haploinsufficient mice

Genes Brain Behav. 2015 Feb;14(2):145-57. doi: 10.1111/gbb.12192. Epub 2015 Feb 10.

Abstract

Aggression is an aspect of social behavior that can be elevated in some individuals with autism spectrum disorder (ASD) and a concern for peers and caregivers. Mutations in Phosphatase and tensin homolog (PTEN), one of several ASD risk factors encoding negative regulators of the PI3K-Akt-mTOR pathway, have been reported in individuals with ASD and comorbid macrocephaly. We previously showed that a mouse model of Pten germline haploinsufficiency (Pten(+/-) ) has selective deficits, primarily in social behavior, along with broad overgrowth of the brain. Here, we further examine the social behavior of Pten(+/-) male mice in the resident-intruder test of aggression, using a comprehensive behavioral analysis to obtain an overall picture of the agonistic, non-agonistic and non-social behavior patterns of Pten(+/-) mice during a free interaction with a novel conspecific. Pten(+/-) male mice were involved in less aggression than their wild-type littermates. Pten(+/-) mice also performed less social investigation, including anogenital investigation and approaching and/or attending to the intruder, which is consistent with our previous finding of decreased sociability in the social approach test. In contrast to these decreases in social behaviors, Pten(+/-) mice showed increased digging. In summary, we report decreased aggression and increased repetitive behavior in Pten(+/-) mice, thus extending our characterization of this model of an ASD risk factor that features brain overgrowth and social deficits.

Keywords: Aggression; Pten; autism; repetitive behavior; resident-intruder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggression / psychology*
  • Animals
  • Behavior, Animal / physiology*
  • Brain / metabolism*
  • Disease Models, Animal
  • Genotype
  • Haploinsufficiency / genetics
  • Haploinsufficiency / physiology*
  • Male
  • Mice, Inbred C57BL
  • PTEN Phosphohydrolase / genetics*
  • Phosphatidylinositol 3-Kinases / metabolism

Substances

  • Phosphatidylinositol 3-Kinases
  • PTEN Phosphohydrolase
  • Pten protein, mouse