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Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling
被引:217
作者:
Hashimoto, Ryota
Numakawa, Tadahiro
Ohnishi, Takashi
Kumamaru, Emi
Yagasaki, Yuki
Ishimoto, Tetsuya
Mori, Takeyuki
Nemoto, Kiyotaka
Adachi, Naoki
Izumi, Aiko
Chiba, Sachie
Noguchi, Hiroko
Suzuki, Tatsuyo
Iwata, Nakao
Ozaki, Norio
Taguchi, Takahisa
Kamiya, Atsushi
Kosuga, Asako
Tatsumi, Masahiko
Kamijima, Kunitoshi
Weinberger, Daniel R.
Sawa, Akira
Kunugi, Hiroshi
机构:
[1] Osaka Univ, Osaka Hamamtsu Joint Res Ctr Child Mental Dev, Grad Sch Med, Osaka 5650871, Japan
[2] Osaka Univ, Dept Psychiat, Grad Sch Med, Osaka 5650871, Japan
[3] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Mental Disorder Res, Kodaira, Tokyo 187, Japan
[4] Natl Ctr Neurol & Psychiat, Natl Ctr Hosp Mental Nervous & Muscular Disorders, Dept Radiol, Kodaira, Tokyo 187, Japan
[5] Natl Inst Adv Ind Sci & Technol, Neuron RG Special Div Human Life Technol, Ikeda, Osaka, Japan
[6] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, Koganei, Tokyo, Japan
[7] Fujita Hlth Univ, Sch Med, Dept Psychiat, Toyoake, Aichi 47011, Japan
[8] Nagoya Univ, Dept Psychiat, Grad Sch Med, Nagoya, Aichi, Japan
[9] Johns Hopkins Univ, Dept Psychiat, Baltimore, MD 21205 USA
[10] Showa Univ, Sch Med, Dept Psychiat, Tokyo 142, Japan
[11] NIMH, Genes Cognit & Psychosis Program, Clin Brain Disorders Branch, NIH, Bethesda, MD 20892 USA
[12] Johns Hopkins Univ, Sch Med, Program Cellular Mol Med, Dept Neurosci, Baltimore, MD USA
[13] Johns Hopkins Univ, Sch Med, Program Cellular Mol Med, Dept Psychiat, Baltimore, MD USA
关键词:
D O I:
10.1093/hmg/ddl244
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Disrupted-in-schizophrenia 1 (DISC1), identified in a pedigree with a familial psychosis with the chromosome translocation (1:11), is a putative susceptibility gene for psychoses such as schizophrenia and bipolar disorder. Although there are a number of patients with major depressive disorder (MDD) in the family members with the chromosome translocation, the possible association with MDD has not yet been studied. We therefore performed an association study of the DISC1 gene with MDD and schizophrenia. We found that Cys704 allele of the Ser704Cys single-nucleotide polymorphism (SNP) was associated with an increased risk of developing MDD (P=0.005, odds ratio=1.46) and stronger evidence for association in a multi-marker haplotype analysis containing this SNP (P=0.002). We also explored possible impact of Ser704Cys on brain morphology in healthy volunteers using MR imaging. We found a reduction in gray matter volume in cingulate cortex and a decreased fractional anisotropy in prefrontal white matter of individuals carrying the Cys704 allele compared with Ser/Ser704 subjects. In primary neuronal culture, knockdown of endogenous DISC1 protein by small interfering RNA resulted in the suppression of phosphorylation of ERK and Akt, whose signaling pathways are implicated in MDD. When effects of sDISC1 (Ser704) and cDISC1 (Cys704) proteins were examined separately, phosphorylation of ERK was greater in sDISC1 compared with cDISC1. A possible biological mechanism of MDD might be implicated by these convergent data that Cys704 DISC1 is associated with the lower biological activity on ERK signaling, reduced brain gray matter volume and an increased risk for MDD.
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页码:3024 / 3033
页数:10
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