Genetic regulation of microRNAs in the older adult brain and their contribution to neuropsychiatric conditions

Selina M Vattathil, Ekaterina S Gerasimov, Se Min Canon, Adriana Lori, Sarah Sze Min Tan, Paul J Kim, Yue Liu, Eric C Lai, David A C. Bennett, Thomas S Wingo, Aliza P Wingo
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Abstract

MicroRNAs are essential post-transcriptional regulators of gene expression and involved in many biological processes; however, our understanding of their genetic regulation and role in brain illnesses is limited. Here, we mapped brain microRNA expression quantitative trait loci (miR-QTLs) using genome-wide small RNA sequencing profiles from dorsolateral prefrontal cortex (dlPFC) samples of 604 older adult donors of European ancestry. miR-QTLs were identified for 224 miRNAs (48% of 470 tested miRNAs) at false discovery rate < 1%. We found that miR-QTLs were enriched in brain promoters and enhancers, and that intragenic miRNAs often did not share QTLs with their host gene. Additionally, we integrated the brain miR-QTLs with results from 16 GWAS of psychiatric and neurodegenerative diseases using multiple independent integration approaches and identified four miRNAs that contribute to the pathogenesis of bipolar disorder, major depression, post-traumatic stress disorder, schizophrenia, and Parkinson's disease. This study provides novel insights into the contribution of miRNAs to the complex biological networks that link genetic variation to disease.
老年人大脑中 microRNA 的遗传调控及其对神经精神疾病的影响
微RNA是基因表达的重要转录后调控因子,参与了许多生物过程;然而,我们对它们的遗传调控及其在脑部疾病中的作用了解有限。在这里,我们利用全基因组小 RNA 测序图谱绘制了脑部 microRNA 表达定量性状位点(miR-QTLs),这些图谱来自 604 名欧洲血统的老年供体的背外侧前额叶皮层(dlPFC)样本。我们发现,miR-QTLs 富集在大脑启动子和增强子中,基因内的 miRNA 通常与其宿主基因不共享 QTLs。此外,我们使用多种独立的整合方法,将脑部 miR-QTL 与 16 种精神疾病和神经退行性疾病的 GWAS 结果进行了整合,发现了四种 miRNA,它们有助于双相情感障碍、重度抑郁症、创伤后应激障碍、精神分裂症和帕金森病的发病机制。这项研究为了解 miRNA 对将遗传变异与疾病联系起来的复杂生物网络的贡献提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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