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The Use of a Comprehensive Behavioral Test Battery on Genetically Engineered Mice
a Horizontal Medical Research Organization, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan b Institute for Bioinformatics Research and Development (BIRD), JST, Japan
Key Words: comprehensive behavioral test battery • psychiatric diseases • genetically engineered mice • animal model of schizophrenia • calcineurin
Address for correspondence: Tsuyoshi Miyakawa, Ph.D., Horizontal Medical Research Organization, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Kyoto 606-8501, Japan. Voice: +81-75-753-9325; fax: +81-75-753-9281. e-mail: miyakawa{at}hmro.med.kyoto-u.ac.jp
We have been investigating the relationships between genes and behaviors by conducting a systematic and well-defined behavioral test battery with mice that have a mutation on a gene of interest. The behavioral test battery covers a relatively broad range of various behavioral domains such as learning and memory, sensory-motor functions, emotion, motivation, and drug sensitivity/preference. Recently, we subjected mice lacking calcineurin (CN), a calcium/calmodulin protein phosphatase, to the comprehensive behavioral test battery. The mutant mice had a severe working memory deficit, increased locomotor activity, decreased social interaction, and impairments in prepulse and latent inhibition. The abnormalities of CN mutant mice were strikingly similar to those described for schizophrenic patients. Consistent with these findings, human genetics studies in a large sample of affected families detected a significant association of the PPP3CC gene, which encodes the CN gamma catalytic subunit with schizophrenia. The idea that abnormalities in the CN signaling pathway are involved in schizophrenia pathogenesis is consistent with traditional theories of schizophrenia and with many facts known about schizophrenia. A tremendous amount of knowledge about CN has accumulated and, by utilizing this information, the studies on the pathogenesis/pathophysiology of schizophrenia and its related mental disorders will be potentially accelerated. We discuss the potential impact of a large-scale mouse phenotyping project on the study of psychiatric disorders.
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