Tang Ruqi, Zhao Xinzhi, Fang Chao, Tang Wei, Huang Ke, Wang Lei, Li Huafang, Feng Guoyin, Zhu Shaomin, Liu Huijun, He Lin, Shi Yongyong
Bio-X Center, Shanghai Jiao Tong University, Shanghai, China.
Neurosci Lett. 2008 May 23;437(1):42-4. doi: 10.1016/j.neulet.2008.03.043. Epub 2008 Mar 21.
The PIK3C3 gene has been implicated as a candidate gene for schizophrenia by functional evidence and genetic association studies. A series of previous studies have found susceptibility SNPs in promoter region. To further verify its susceptibility to schizophrenia in the Chinese population and the function of the polymorphisms, we performed a case control study in 556 unrelated schizophrenia patients and 563 normal controls as well as an in vitro functional analysis. In our association analysis of-432C-/T, we discovered obvious differences in allele frequency between patients and controls (P=0.017). A T/C haplotype constructed by -432C-/T and -86insC, which are tightly linked with each other (r(2)=1) can significantly weaken promoter's transcriptional activity by 20% (p=0.002 by t-test). Though we cannot exclude the possibility that susceptibility of -432C-/T is caused by its linkage disequilibrium with other causal variants, our results do support PIK3C3 play a significant role in the etiology of schizophrenia.
通过功能证据和基因关联研究,PIK3C3基因被认为是精神分裂症的候选基因。此前一系列研究已在启动子区域发现了易感单核苷酸多态性(SNP)。为进一步验证其在中国人群中对精神分裂症的易感性及多态性的功能,我们对556名无亲缘关系的精神分裂症患者和563名正常对照进行了病例对照研究,并进行了体外功能分析。在我们对-432C/T的关联分析中,我们发现患者和对照之间的等位基因频率存在明显差异(P=0.017)。由-432C/T和-86insC构建的T/C单倍型,它们彼此紧密连锁(r²=1),可使启动子的转录活性显著降低20%(t检验,p=0.002)。尽管我们不能排除-432C/T的易感性是由其与其他致病变异的连锁不平衡所导致的可能性,但我们的结果确实支持PIK3C3在精神分裂症病因学中起重要作用。