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Noncanonical cytoplasmic processing of viral microRNAs

机译:病毒microRNA的非规范细胞质加工

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摘要

Cellular utilization of RNA interference (RNAi) as a mechanism to combat virus infection is thought to be restricted to plants and invertebrates. In vertebrates, antiviral defenses are largely dependent on interferons (IFNs), with the use of small RNAs restricted to microRNA (miRNA)–mediated targeting of host transcripts. Here we demonstrate that incorporation of a primary miRNA into a cytoplasmic virus results in the formation of a Dicer-dependent, DGCR8-independent, mature miRNA capable of conferring RNAi-like activity. Processing of the viral mirtron-like product (virtron) is indistinguishable from endogenous miRNA maturation and elicits post-transcriptional gene silencing, albeit at a reduced level. Furthermore, virtrons impose Dicer-dependent, microprocessor-independent, and IFN-independent interference on virus replication in a sequence-specific manner. Taken together, these results suggest the existence of a noncanonical, small-RNA-based activity capable of processing cytoplasmic hairpins and perhaps contributing to the cell's antiviral arsenal.
机译:RNA干扰(RNAi)作为对抗病毒感染的机制在细胞中的利用被认为仅限于植物和无脊椎动物。在脊椎动物中,抗病毒防御很大程度上取决于干扰素(IFN),并使用仅限于microRNA(miRNA)介导的宿主转录物的小RNA。在这里,我们证明了将原始miRNA掺入细胞质病毒会导致Dicer依赖,DGCR8独立,能够赋予RNAi活性的成熟miRNA形成。病毒性mirtron样产物(virtron)的加工与内源性miRNA成熟没有区别,并引起转录后基因沉默,尽管水平较低。此外,virtrons以序列特异性方式对病毒复制施加Dicer依赖性,微处理器依赖性和IFN依赖性干扰。综上所述,这些结果表明存在一种非典型的,基于小RNA的活性,该活性能够处理细胞质发夹,并可能有助于细胞的抗病毒药库。

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