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Association analysis of the DISC1 gene with schizophrenia in the Japanese population and DISC1 immunoreactivity in the postmortem brain
Authors:Woraphat Ratta-apha  Akitoyo Hishimoto  Kentaro Mouri  Kyoichi Shiroiwa  Toru Sasada  Masakuni Yoshida  Irwan Supriyanto  Yasuhiro Ueno  Migiwa Asano  Osamu Shirakawa  Hideru Togashi  Yoshimi Takai  Ichiro Sora
Affiliation:1. Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan;2. Department of Legal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan;3. Department of Legal Medicine, Ehime University Graduate School of Medicine, Ehime, Japan;4. Department of Neuropsychiatry, Kinki University School of Medicine, Osaka, Japan;5. Division of Molecular and Cellular Biology, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe, Japan
Abstract:
The Disrupted-in-Schizophrenia 1 (DISC1) gene plays a role in the regulation of neural development. Previous evidence from genetic association and biological studies implicates the DISC1 gene as having a role in the pathophysiology of schizophrenia. In the present study, we explored the association between DISC1 missense mutation rs821616 (Ser704Cys) single nucleotide polymorphism (SNP) and four other SNPs (rs1772702, rs1754603, rs821621, rs821624) in the related haplotype block and schizophrenia in the Japanese population. We could not find a significant association of selected SNPs with schizophrenia after correction for multiple testing. We performed a meta-analysis of the Ser704Cys variant in schizophrenia using data from the present study and five previous Japanese population studies, and found no association with schizophrenia. We also examined DISC1 immunoreactivity in postmortem prefrontal cortex specimens of schizophrenia patients compared to control samples. The immunoreactivity revealed a significant decrease of DISC1 protein expression in the schizophrenia samples after ruling out potential confounding factors. However, the Ser704Cys variant did not show effects on DISC1 immunoreactivity. These results provide evidence that this functional genetic variation of DISC1 do not underlie the pathophysiology of schizophrenia in the Japanese population.
Keywords:DISC1, Disrupted-in-Schizophrenia 1   SNP, single nucleotide polymorphism   HWE, Hardy&ndash  Weinberg equilibrium   LD, linkage disequilibrium   DLPFC, dorsolateral prefrontal cortex
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