Dscam gene triplication causes neocortical overinhibition in Down syndrome

A growing number of molecules have been identified as regulators of inhibitory synapse development, but whether dysregulated expression of these molecules contribute to brain disorders is poorly understood. Here we show that Down syndrome cell adhesion molecule () regulates the inhibition of neocortical pyramidal neurons (PyNs) in a level-dependent fashion. Loss of impairs inhibitory neuron development and function. In the Ts65Dn mouse model for Down syndrome, where is overexpressed, GABAergic innervation of cortical PyNs by chandelier and basket cells is increased. Genetic normalization of expression rescues the excessive GABAergic innervation and the increased inhibition of PyNs. These findings demonstrate excessive GABAergic innervation and inhibition in the neocortex of Down syndrome mouse model and identify overexpression as the cause. They also implicate dysregulated levels as a potential pathogenic driver in related neurological disorders.