TY - JOUR T1 - Haploinsufficiency of autism candidate gene NUAK1 impairs cortical development and behavior JF - bioRxiv DO - 10.1101/262725 SP - 262725 AU - Virginie Courchet AU - Amanda J Roberts AU - Peggy Del Carmine AU - Tommy L. Lewis, Jr AU - Franck Polleux AU - Julien Courchet Y1 - 2018/01/01 UR - http://biorxiv.org/content/early/2018/02/09/262725.abstract N2 - Recently, numerous rare de novo mutations have been identified in children diagnosed with autism spectrum disorders (ASD). However, despite the predicted loss-of-function nature of some of these de novo mutations, the affected individuals are heterozygous carriers, which would suggest that most of these candidate genes are haploinsufficient and/or that these mutations lead to expression of dominant-negative forms of the protein. Here, we tested this hypothesis with the gene Nuak1, recently identified as a candidate ASD gene and that we previously identified for its role in the development of cortical connectivity. We report that Nuak1 is happloinsufficient in mice in regard to its function in cortical axon branching in vitro and in vivo. Nuak1+/− mice show a combination of abnormal behavioral traits ranging from defective memory consolidation in a spatial learning task, defects in social novelty (but not social preference) and abnormal sensorimotor gating and prepulse inhibition of the startle response. Overall, our results demonstrate that Nuak1 haploinsufficiency leads to defects in the development of cortical connectivity and a complex array of behavorial deficits compatible with ASD, intellectual disability and schizophrenia. ER -