AUTS2 regulation of synapses for proper synaptic inputs and social communication

<jats:title>Abstract</jats:title><jats:p>Impairments in synapse development are thought to cause numerous psychiatric disorders.<jats:italic>Autism susceptibility candidate 2</jats:italic>(<jats:italic>AUTS2</jats:italic>) gene has been associated with various psychiatric disorders, such as autism and intellectual disabilities. Although roles for AUTS2 in neuronal migration and neuritogenesis have been reported, its involvement in synapse regulation remains unclear. In this study, we found that excitatory synapses were specifically increased in the<jats:italic>Auts2</jats:italic>-deficient primary cultured neurons as well as<jats:italic>Auts2</jats:italic>mutant forebrains. Electrophysiological recordings and immunostaining showed increases in excitatory synaptic inputs as well as c-fos expression in<jats:italic>Auts2</jats:italic>mutant brains, suggesting that an altered balance of excitatory and inhibitory inputs enhances brain excitability.<jats:italic>Auts2</jats:italic>mutant mice exhibited autistic-like behaviors including impairments in social interaction and altered vocal communication. Together, these findings suggest that AUTS2 regulates excitatory synapse number to coordinate E/I balance in the brain, whose impairment may underlie the pathology of psychiatric disorders in individuals with<jats:italic>AUTS2</jats:italic>mutations.</jats:p>