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Regulation of Huntingtin Gene Expression by miRNA-137, -214, -148a, and Their Respective isomiRs

机译:miRNA-137,-214,-148a及其各自的isoomiR对Huntingtin基因表达的调控

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With the advent of deep sequencing technology, a variety of miRNA length and sequence variants, termed isomiRNAs (isomiRs), have been discovered. However, the functional roles of these commonly detected isomiRs remain unknown. In this paper, we demonstrated that miRNAs regulate the expression of the HTT gene, whose mutation leads to Huntington’s disease (HD), a hereditary degenerative disorder. Specifically, we validated the interactions of canonical miRNAs, miR-137, miR-214, and miR-148a, with the HTT 3′UTR using a luciferase assay. Moreover, we applied synthetic miRNA mimics to examine whether a slight shifting of miRNA seed regions might alter the regulation of the HTT transcript. We also examined miR-137, miR-214, and miR-148a isomiRs and showed the activity of these isoforms on reporter constructs bearing appropriate sequences from the HTT 3′UTR. Hence, we demonstrated that certain 5′-end variants of miRNAs might be functional for the regulation of the same targets as canonical miRNAs.
机译:随着深度测序技术的出现,人们发现了多种称为isomiRNA(isomiR)的miRNA长度和序列变体。但是,这些通常检测到的isomiR的功能角色仍然未知。在本文中,我们证明了miRNA调节HTT基因的表达,该基因的突变会导致亨廷顿舞蹈病(HD),一种遗传性变性疾病。具体来说,我们使用萤光素酶测定法验证了规范性miRNA,miR-137,miR-214和miR-148a与HTT 3'UTR的相互作用。此外,我们应用合成的miRNA模拟物来检查miRNA种子区域的轻微移动是否会改变HTT转录物的调控。我们还检查了miR-137,miR-214和miR-148a isomiRs,并显示了这些同工型在带有来自HTT 3'UTR的适当序列的报告基因构建体上的活性。因此,我们证明了miRNA的某些5'端变体可能具有与规范miRNA相同的靶标调控功能。

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