精神分裂症风险相关 SNPs 对 microRNA 137 宿主基因表达的影响:一项尸检研究。

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ningping Feng, Ajeet Mandal, Ananya Jambhale, Pranav Narnur, Gang Chen, Nirmala Akula, Robin Kramer, Bhaskar Kolachana, Qing Xu, Francis J McMahon, Barbara K Lipska, Pavan K Auluck, Stefano Marenco
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引用次数: 0

摘要

MicroRNA 137 宿主基因 MIR137HG 及其邻近基因 DPYD 的常见变异与精神分裂症风险有关,而最新的精神疾病基因组学联盟(PGC)精神分裂症全基因组关联研究(Genome-Wide Association Study on schizophrenia)证实并扩展了这些发现。精神分裂症的全基因组关联研究证实并扩展了这些发现。为了阐明精神分裂症风险相关 SNPs 与该基因组区域的关联,我们使用 qPCR 和 RNA-Seq 方法检测了 miR-137 宿主基因(MIR137HG)在精神分裂症供体和未受精神疾病影响的对照组死后大脑样本的背外侧前额叶皮层(DLPFC)和舌下前扣带回皮层(sgACC)中成熟和未成熟转录本的表达。没有观察到 miR-137、MIR137HG 或其转录物的差异表达。在 PGC 研究中发现的两个精神分裂症风险相关 SNPs: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 转录本 MIR137HG-203 (ENST00000602672.2) 的表达相关。与携带主要等位基因的人相比,rs11165917 的次要(风险)等位基因携带者的 MIR137HG-203 表达量明显较低。然而,我们无法通过对从 DLPFC 或 sgACC 组织中提取的 RNA 进行短线程测序来验证这一结果。这一发现表明,MIR137HG的未成熟转录本可能会导致精神分裂症的遗传风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Schizophrenia risk-associated SNPs affect expression of microRNA 137 host gene: a postmortem study.

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.

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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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