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痘病毒多聚(A)聚合酶降解宿主 microRNAs 揭示了末端 RNA 甲基化作为一种保护性抗病毒机制。

Degradation of host microRNAs by poxvirus poly(A) polymerase reveals terminal RNA methylation as a protective antiviral mechanism.

机构信息

Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Cell Host Microbe. 2012 Aug 16;12(2):200-10. doi: 10.1016/j.chom.2012.05.019.

Abstract

The life cycle of several viruses involves host or virally encoded small noncoding RNAs, which play important roles in posttranscriptional regulation. Small noncoding RNAs include microRNAs (miRNAs), which modulate the transcriptome, and small interfering RNAs (siRNAs), which are involved in pathogen defense in plants, worms, and insects. We show that insect and mammalian poxviruses induce the degradation of host miRNAs. The virally encoded poly(A) polymerase, which polyadenylates viral transcripts, also mediates 3' polyadenylation of host miRNAs, resulting in their degradation by the host machinery. In contrast, siRNAs, which are protected by 2'O-methylation (2'OMe), were not targeted by poxviruses. These findings suggest that poxviruses may degrade host miRNAs to promote replication and that virus-mediated small RNA degradation likely contributed to 2'OMe evolution.

摘要

几种病毒的生命周期涉及宿主或病毒编码的小型非编码 RNA,它们在后转录调控中发挥重要作用。小型非编码 RNA 包括 microRNAs(miRNAs),其调节转录组,以及 small interfering RNAs(siRNAs),其参与植物、蠕虫和昆虫中的病原体防御。我们表明,昆虫和哺乳动物痘病毒诱导宿主 miRNAs 的降解。病毒编码的 poly(A) 聚合酶,其对病毒转录物进行 poly(A) 加尾,也介导宿主 miRNAs 的 3' poly(A) 加尾,导致它们被宿主机制降解。相比之下,受 2'O-甲基化(2'OMe)保护的 siRNAs 不受痘病毒的靶向。这些发现表明,痘病毒可能会降解宿主 miRNAs 以促进复制,并且病毒介导的小 RNA 降解可能有助于 2'OMe 的进化。

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