Umeda-Yano Satomi, Hashimoto Ryota, Yamamori Hidenaga, Weickert Cynthia Shannon, Yasuda Yuka, Ohi Kazutaka, Fujimoto Michiko, Ito Akira, Takeda Masatoshi
Department of Molecular Neuropsychiatry, Osaka University Graduate School of Medicine, Suita, Osaka 5650871, Japan.
Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka 5650871, Japan; Molecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University, Suita, Osaka 5650871, Japan.
Neurosci Lett. 2014 May 7;568:12-6. doi: 10.1016/j.neulet.2014.03.031. Epub 2014 Mar 28.
Many gene expression studies have examined postmortem brain tissues of patients with schizophrenia. However, only a few expression studies of the genes identified in genome-wide association study (GWAS) have been published to date. We measured the expression levels of the genes identified in GWAS (ZNF804A, OPCML, RPGRIP1L, NRGN, and TCF4) of the postmortem brain tissues of patients with schizophrenia and controls from two separate sample sets (i.e., the Australian Tissue Resource Center and Stanley Medical Research Institute). We also determined whether the single-nucleotide polymorphisms (SNPs) identified in the GWAS were related to the gene expression changes in the prefrontal cortex. No difference was observed between the patients with schizophrenia and controls from the Australian Tissue Resource Center samples in the mRNA levels of ZNF804A, OPCML, RPGRIP1L, NRGN, or TCF4. The lack of mRNA change for these five transcripts was also found in the brain samples from the Stanley Medical Research Institute. In addition, no relationship between the schizophrenia-associated SNPs identified in the GWAS and the corresponding gene expression was observed in either sample set. Our results suggest that major changes in the transcript levels of the five candidate genes identified in the GWAS may not occur in adult patients with schizophrenia. The lack of linkage between the risk gene polymorphisms and the expression levels of their major transcripts suggests that the control of pan mRNA levels may not be a prominent mechanism by which the genes identified in the GWAS contribute to the pathophysiology of schizophrenia. Further studies are needed to examine how the genes identified in the GWAS contribute to the pathophysiology of schizophrenia.
许多基因表达研究都对精神分裂症患者的死后脑组织进行了检测。然而,迄今为止,在全基因组关联研究(GWAS)中鉴定出的基因,仅有少数表达研究得以发表。我们测量了来自两个独立样本集(即澳大利亚组织资源中心和斯坦利医学研究所)的精神分裂症患者及对照者死后脑组织中GWAS鉴定出的基因(ZNF804A、OPCML、RPGRIP1L、NRGN和TCF4)的表达水平。我们还确定了GWAS中鉴定出的单核苷酸多态性(SNP)是否与前额叶皮质中的基因表达变化相关。在澳大利亚组织资源中心样本中,精神分裂症患者与对照者在ZNF804A、OPCML、RPGRIP1L、NRGN或TCF4的mRNA水平上未观察到差异。在斯坦利医学研究所的脑样本中也发现这五个转录本缺乏mRNA变化。此外,在任一样本集中均未观察到GWAS中鉴定出的与精神分裂症相关的SNP与相应基因表达之间存在关联。我们的结果表明,GWAS中鉴定出的五个候选基因的转录水平在成年精神分裂症患者中可能不会发生重大变化。风险基因多态性与其主要转录本的表达水平之间缺乏联系,这表明控制泛mRNA水平可能不是GWAS中鉴定出的基因促成精神分裂症病理生理学的突出机制。需要进一步研究来探讨GWAS中鉴定出的基因如何促成精神分裂症的病理生理学。