Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Autism spectrum conditions (ASCs) are heritable conditions characterized by impaired reciprocal social interactions, deficits in language acquisition, and repetitive and restricted behaviors and interests. In addition to more complex genetic susceptibilities, even mutation of a single gene can lead to ASC. Several such monogenic heritable ASC forms are caused by loss-of-function mutations in genes encoding regulators of synapse function in neurons, including NLGN4. We report that mice with a loss-of-function mutation in the murine NLGN4 ortholog Nlgn4, which encodes the synaptic cell adhesion protein Neuroligin-4, exhibit highly selective deficits in reciprocal social interactions and communication that are reminiscent of ASCs in humans. Our findings indicate that a protein network that regulates the maturation and function of synapses in the brain is at the core of a major ASC susceptibility pathway, and establish Neuroligin-4-deficient mice as genetic models for the exploration of the complex neurobiological disorders in ASCs.
Pubmed ID: 18227507 RIS Download
Amino Acid Sequence | Animals | Autistic Disorder | Brain | Carrier Proteins | Cell Adhesion Molecules, Neuronal | Communication | Disease Models, Animal | Membrane Proteins | Memory | Mice | Mice, Knockout | Molecular Sequence Data | Organ Size | Social Behavior | Synapses | Ultrasonics | Vocalization, Animal