Rastogi Anjali, Zai Clement, Likhodi Olga, Kennedy James L, Wong Albert H
Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, Canada.
Schizophr Res. 2009 Oct;114(1-3):39-49. doi: 10.1016/j.schres.2009.06.019. Epub 2009 Jul 24.
Convergent evidence from genetic linkage, genetic association and biological studies implicates the Disrupted in schizophrenia 1 (DISC1) gene in the etiology and pathophysiology of schizophrenia. We conducted genetic association studies in matched case-control and family sample sets (N=117 families; N=210 case-control pairs), testing polymorphisms across DISC1 and DISC1 interacting genes: LIS1, NUDEL, FEZ1 and PDE4B. We found that DISC1 variants, particularly in the exon 9/intron 9/intron 10 region of the gene, may be associated with risk for schizophrenia in our sample population. There was no strong evidence for association with LIS1, NUDEL, FEZ1 and PDE4B. Gene-gene interaction analyses and mRNA quantification in post-mortem brains from schizophrenia patients and control subjects did not reveal significant differences.
来自基因连锁、基因关联和生物学研究的汇聚证据表明,精神分裂症1号基因(DISC1)与精神分裂症的病因学和病理生理学有关。我们在匹配的病例对照和家系样本组中进行了基因关联研究(N = 117个家系;N = 210对病例对照),检测了DISC1及其相互作用基因LIS1、NUDEL、FEZ1和PDE4B的多态性。我们发现,DISC1变异,尤其是该基因外显子9/内含子9/内含子10区域的变异,可能与我们样本群体中精神分裂症的风险相关。没有强有力的证据表明LIS1、NUDEL、FEZ1和PDE4B与之相关。对精神分裂症患者和对照受试者死后大脑进行的基因-基因相互作用分析和mRNA定量分析未发现显著差异。