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Loop-miRs: active microRNAs generated from single-stranded loop regions

机译:Loop-miR:从单链环区产生的活性microRNA

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摘要

MicroRNAs (miRNAs) are key mediators of post-transcriptional gene regulation. The miRNA precursors are processed by the endonucleases Drosha and Dicer into a duplex, bound to an Argonaute protein and unwound into two single-stranded miRNAs. Although alternative ways to generate miRNAs have been discovered, e.g. pre-miRNA cleavage by Ago2 or cleavage products of snoRNAs or tRNAs, all known pathways converge on a double-stranded RNA duplex. Exogenous single-stranded siRNAs (ss-siRNAs) can elicit an effective RNA interference reaction; recent studies have identified chemical modifications increasing their stability and activity. Here, we provide first evidence that endogenous, unmodified, single-stranded RNA sequences are generated from single-stranded loop regions of human pre-miRNA hairpins, the so called loop-miRs. Luciferase assays and immunoprecipitation validate loop-miR activity and incorporation into RNA-induced silencing complexes. This study identifies endogenous miRNAs that are generated from single-stranded regions; hence, it provides evidence that precursor-miRNAs can give rise to three distinct endogenous miRNAs: the guide strand, the passenger strand and the loop-miR.
机译:MicroRNA(miRNA)是转录后基因调控的关键介体。 miRNA前体被核酸内切酶Drosha和Dicer加工成双链体,与Argonaute蛋白结合并解链成两个单链miRNA。尽管已经发现了产生miRNA的其他方法,例如Ago2切割pre-miRNA或snoRNA或tRNA的切割产物,所有已知途径都汇聚在双链RNA双链体上。外源单链siRNA(ss-siRNA)可以引发有效的RNA干扰反应。最近的研究已经发现化学修饰可以增加其稳定性和活性。在这里,我们提供了第一个证据,即从人类pre-miRNA发夹的单链环区域(即所谓的loop-miRs)产生了内源性,未修饰的单链RNA序列。萤光素酶测定法和免疫沉淀法可验证loop-miR活性并将其掺入RNA诱导的沉默复合物中。这项研究鉴定了从单链区域产生的内源性miRNA。因此,它提供了证据,即前体miRNA可以产生三种不同的内源性miRNA:引导链,过客链和loop-miR。

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