1. Disc1Point Mutations in Mice Affect Development of the Cerebral Cortex
- Author
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John C. Roder, Frankie H. F. Lee, David Price, Sabine P. Cordes, Kate Preston-Maher, Steven J. Clapcote, Albert H.C. Wong, and Marc P. Fadel
- Subjects
Candidate gene ,Time Factors ,NEURAL TUBE ,MOUSE ,Mice ,chemistry.chemical_compound ,Pregnancy ,genetics ,genes ,Neurotransmitter ,Cerebral Cortex ,Mice, Knockout ,Neurons ,biology ,General Neuroscience ,Neurogenesis ,Brain ,Articles ,Growth Inhibitors ,medicine.anatomical_structure ,Embryo ,Cerebral cortex ,Schizophrenia ,Female ,EXPRESSION ,Neurite ,Neuroscience(all) ,Mice, Transgenic ,Nerve Tissue Proteins ,Research Support ,Polymorphism, Single Nucleotide ,DISC1 ,Glypicans ,embryology ,medicine ,Point Mutation ,Animals ,development ,Body Patterning ,Research ,medicine.disease ,GENE ,Mice, Inbred C57BL ,Amino Acid Substitution ,chemistry ,Gene Expression Regulation,Developmental ,biology.protein ,Neuron ,Head ,metabolism ,Neuroscience - Abstract
Disrupted-in-Schizophrenia 1 (DISC1) is a strong candidate gene for schizophrenia and other mental disorders. DISC1 regulates neurodevelopmental processes including neurogenesis, neuronal migration, neurite outgrowth, and neurotransmitter signaling. Abnormal neuronal morphology and cortical architecture are seen in human postmortem brain from patients with schizophrenia. However, the etiology and development of these histological abnormalities remain unclear. We analyzed the histology of twoDisc1mutant mice with point mutations (Q31L and L100P) and found a relative reduction in neuron number, decreased neurogenesis, and altered neuron distribution compared to wild-type littermates. Frontal cortical neurons have shorter dendrites and decreased surface area and spine density. Overall, the histology ofDisc1mutant mouse cortex is reminiscent of the findings in schizophrenia. These results provide further evidence thatDisc1participates in cortical development, including neurogenesis and neuron migration.
- Published
- 2011
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