Chen Zhang1, Zhiguo Wu2, Wu Hong2, Daihui Peng2, Yiru Fang3. 1. Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. Electronic address: zhangchen645@gmail.com. 2. Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. 3. Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. Electronic address: yirufang@aliyun.com.
Abstract
BACKGROUND: Previous studies have shown that the genes involved in synaptic density and plasticity were downregulated in bipolar disorder (BD) postmortem brains. The SHANK3 (SH3 and multiple ankyrin repeat domain 3) protein is a scaffold protein enriched in the postsynaptic density of excitatory synapses, and recent findings were suggestive of a possible role of SHANK3 in the development of BD. In this study, we aimed to evaluate the genetic association between the gene encoding SHANK3 (SHANK3) and BD in Han Chinese. METHODS: Ten variants in SHANK3 were genotyped among 1482 individuals with or without BD. We measured the mRNA expression level of SHANK3 in patients with BD and controls. We then performed an eQTL analysis. RESULTS: In our sample set, there were no significant differences in allele, genotype and haplotype frequencies between the BD and control groups. Our results showed no significant difference in the level of peripheral SHANK3 expression between the BD patients and healthy controls. Further eQTL analysis showed that rs9616915 has functional effect on SHANK3 expression in the hippocampus. CONCLUSION: This study does not provide evidence for a major role of SHANK3 in the pathogenesis of BD.
BACKGROUND: Previous studies have shown that the genes involved in synaptic density and plasticity were downregulated in bipolar disorder (BD) postmortem brains. The SHANK3 (SH3 and multiple ankyrin repeat domain 3) protein is a scaffold protein enriched in the postsynaptic density of excitatory synapses, and recent findings were suggestive of a possible role of SHANK3 in the development of BD. In this study, we aimed to evaluate the genetic association between the gene encoding SHANK3 (SHANK3) and BD in Han Chinese. METHODS: Ten variants in SHANK3 were genotyped among 1482 individuals with or without BD. We measured the mRNA expression level of SHANK3 in patients with BD and controls. We then performed an eQTL analysis. RESULTS: In our sample set, there were no significant differences in allele, genotype and haplotype frequencies between the BD and control groups. Our results showed no significant difference in the level of peripheral SHANK3 expression between the BD patients and healthy controls. Further eQTL analysis showed that rs9616915 has functional effect on SHANK3 expression in the hippocampus. CONCLUSION: This study does not provide evidence for a major role of SHANK3 in the pathogenesis of BD.