Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice

• Published in: Scientific reports 2016-01, Vol.6 (1), p.18748-18748, Article 18748
• Main Authors: Dachtler, James, Elliott, Christina, Rodgers, R. John, Baillie, George S., Clapcote, Steven J.
• Format: Article
• Language: English
• Subjects: 45/23; 45/70; 631/208/1515; 631/378/1689/1761; 64; 64/60; 692/4017; 82; 82/1; 82/80; Amino Acid Sequence; Animals; Anxiety - genetics; Avoidance Learning; Behavior, Animal; DNA Mutational Analysis; Female; Glycogen Synthase Kinase 3 beta - metabolism; Humanities and Social Sciences; Hyperkinesis - genetics; Male; Mice; Models, Biological; Motor Activity - genetics; multidisciplinary; Mutation, Missense; Nerve Tissue Proteins - chemistry; Nerve Tissue Proteins - genetics; Nerve Tissue Proteins - metabolism; Phenotype; Protein Interaction Domains and Motifs - genetics; Science; Sex Factors; Signal Transduction; Social Behavior
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep18748

Disrupted-in-Schizophrenia 1 ( DISC1 ) is a risk factor for schizophrenia and affective disorders. The full-length DISC1 protein consists of an N-terminal ‘head’ domain and a C-terminal tail domain that contains several predicted coiled-coils, structural motifs involved in protein-protein interactions. To probe the in vivo effects of missense mutation of DISC1’s C-terminal tail, we tested mice carrying mutation D453G within a predicted α-helical coiled-coil region. We report that, relative to wild-type littermates, female DISC1 D453G mice exhibited novelty-induced hyperlocomotion, an anxiogenic profile in the elevated plus-maze and open field tests and reduced social exploration of unfamiliar mice. Male DISC1 D453G mice displayed a deficit in passive avoidance, while neither males nor females exhibited any impairment in startle reactivity or prepulse inhibition. Whole brain homogenates showed normal levels of DISC1 protein, but decreased binding of DISC1 to GSK3β, decreased phospho-inhibition of GSK3β at serine 9 and decreased levels of β-catenin in DISC1 D453G mice of either sex. Interrupted GSK3β signaling may thus be part of the mechanism underlying the behavioral phenotype associated with D453G, in common with the previously described N-terminal domain mutations Q31L and L100P in mice and the schizophrenia risk-conferring variant R264Q in humans.