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精神分裂症风险相关 SNP 影响 microRNA 137 宿主基因的表达:一项尸检研究。

Schizophrenia risk-associated SNPs affect expression of microRNA 137 host gene: a postmortem study.

机构信息

Human Brain Collection Core, National Institute of Mental Health, Intramural Research Program, National Institutes of Health, 10 Center Drive, Bldg 10, room 4N218, Bethesda, MD 20892, United States.

Scientific and Statistical Computing Core, National Institute of Mental Health, Intramural Research Program, National Institutes of Health, 10 Center Drive, bldg 10, room 1D73, Bethesda, MD 20892, United States.

出版信息

Hum Mol Genet. 2024 Nov 8;33(22):1939-1947. doi: 10.1093/hmg/ddae130.

Abstract

Common variants in the MicroRNA 137 host gene MIR137HG and its adjacent gene DPYD have been associated with schizophrenia risk and the latest Psychiatric Genomics Consortium (PGC). Genome-Wide Association Study on schizophrenia has confirmed and extended these findings. To elucidate the association of schizophrenia risk-associated SNPs in this genomic region, we examined the expression of both mature and immature transcripts of the miR-137 host gene (MIR137HG) in the dorsolateral prefrontal cortex (DLPFC) and subgenual anterior cingulate cortex (sgACC) of postmortem brain samples of donors with schizophrenia and psychiatrically-unaffected controls using qPCR and RNA-Seq approaches. No differential expression of miR-137, MIR137HG, or its transcripts was observed. Two schizophrenia risk-associated SNPs identified in the PGC study, rs11165917 (DLPFC: P = 2.0e-16; sgACC: P = 6.4e-10) and rs4274102 (DLPFC: P = 0.036; sgACC: P = 0.002), were associated with expression of the MIR137HG long non-coding RNA transcript MIR137HG-203 (ENST00000602672.2) in individuals of European ancestry. Carriers of the minor (risk) allele of rs11165917 had significantly lower expression of MIR137HG-203 compared with those carrying the major allele. However, we were unable to validate this result by short-read sequencing of RNA extracted from DLPFC or sgACC tissue. This finding suggests that immature transcripts of MIR137HG may contribute to genetic risk for schizophrenia.

摘要

常见的 MicroRNA 137 宿主基因 MIR137HG 及其相邻基因 DPYD 的变体与精神分裂症风险有关,最新的精神疾病基因组联合会 (PGC) 全基因组关联研究已经证实并扩展了这些发现。为了阐明该基因组区域中与精神分裂症风险相关的 SNP 的关联,我们使用 qPCR 和 RNA-Seq 方法检查了死后大脑样本中外侧前额叶皮层 (DLPFC) 和前扣带皮层下亚区 (sgACC) 中 miR-137 宿主基因 (MIR137HG) 的成熟和不成熟转录物的表达。未观察到 miR-137、MIR137HG 或其转录物的差异表达。在 PGC 研究中鉴定出的两个与精神分裂症相关的风险 SNP,rs11165917 (DLPFC: P = 2.0e-16; sgACC: P = 6.4e-10) 和 rs4274102 (DLPFC: P = 0.036; sgACC: P = 0.002),与欧洲血统个体中 MIR137HG 长非编码 RNA 转录物 MIR137HG-203 (ENST00000602672.2) 的表达相关。与携带主要等位基因的个体相比,rs11165917 的次要(风险)等位基因的携带者的 MIR137HG-203 表达明显降低。然而,我们无法通过从 DLPFC 或 sgACC 组织中提取的 RNA 的短读测序来验证这一结果。这一发现表明,MIR137HG 的不成熟转录物可能导致精神分裂症的遗传风险。

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