School of Medicine, Tsinghua University, Hai Dian District, Beijing 100084, PR China.
Schizophr Res. 2010 Jun;119(1-3):219-27. doi: 10.1016/j.schres.2010.02.1070. Epub 2010 Mar 27.
MicroRNAs (miRNAs) are short, non-coding RNAs that regulate the stability and translation of mRNA targets. Increasing evidence suggests that miRNAs could be involved in the initiation and progression of neuropsychiatric disorders. Prior to this study, six miRNAs had been reported to show a significantly abnormal expression level in schizophrenic brains. Also, common single nucleotide polymorphisms within two miRNA transcripts have shown genetic associations with schizophrenia. However, it remains largely unknown whether variants in these miRNA genes and/or in their target sites are associated with schizophrenia. Here, we selected the above eight miRNAs, plus 15 of their experimentally validated target sites, as candidate susceptibility factors for schizophrenia, for mutation screening and further association studies in Chinese case-control samples. We identified a new potentially functional variant ss178077483 located in the pre-mir-30e, which was strongly associated with schizophrenia (allelic P=0.00017; genotypic P=0.00015), with an odds ratio of 4.952 (95% confidence interval: 1.887-12.998). We also demonstrated that this new variant ss178077483, combined with mir-30e rs7556088 and mir-24-MAPK14 rs3804452, showed a weak gene-gene interaction for schizophrenia risk (P=0.001). In addition, analysis of gene expression demonstrated that expression of the mature mir-30e in the peripheral leukocytes was significantly higher in patients' group than in the control group (P=6.79e-7).This is the first study to indicate that mir-30e ss178077483 plays a role in schizophrenia susceptibility. It suggests that the contribution of mir-30e to the processes that lead to schizophrenia should be further investigated.
微小 RNA(miRNAs)是一类短的非编码 RNA,能够调控 mRNA 靶标的稳定性和翻译。越来越多的证据表明,miRNAs 可能参与了神经精神疾病的发生和发展。在此之前,已有 6 种 miRNAs 被报道在精神分裂症患者的大脑中表现出显著的异常表达水平。此外,两个 miRNA 转录本中的常见单核苷酸多态性已显示与精神分裂症存在遗传关联。然而,miRNA 基因及其靶位点的变异是否与精神分裂症有关,在很大程度上仍不清楚。在此,我们选择了上述 8 种 miRNAs 以及它们的 15 个经实验验证的靶位点作为候选易感因素,对中国病例对照样本进行突变筛选和进一步的关联研究。我们发现了一个位于 pre-mir-30e 中的新的潜在功能变体 ss178077483,它与精神分裂症强烈相关(等位基因 P=0.00017;基因型 P=0.00015),优势比为 4.952(95%置信区间:1.887-12.998)。我们还证明,这个新的变体 ss178077483 与 mir-30e rs7556088 和 mir-24-MAPK14 rs3804452 联合,对精神分裂症风险表现出较弱的基因-基因相互作用(P=0.001)。此外,基因表达分析表明,外周血白细胞中成熟 mir-30e 的表达在患者组中明显高于对照组(P=6.79e-7)。这是第一项表明 mir-30e ss178077483 参与精神分裂症易感性的研究。这表明,mir-30e 对导致精神分裂症的过程的贡献应该进一步研究。