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RNA介导的微小RNA降解:一种广泛存在的病毒策略?

RNA-mediated degradation of microRNAs: A widespread viral strategy?

作者信息

McCaskill Jana, Praihirunkit Pairoa, Sharp Paul M, Buck Amy H

机构信息

a Institute of Immunology and Infection Research; School of Biological Sciences; University of Edinburgh ; Edinburgh , UK.

出版信息

RNA Biol. 2015;12(6):579-85. doi: 10.1080/15476286.2015.1034912.

Abstract

Regulation of small RNAs by other non-coding RNAs is a ubiquitous feature of gene regulatory systems that can be exploited by viruses. Examples of this have been described in 3 different herpesviruses, where viral non-coding RNAs bind to highly abundant cellular (miRNAs), mediating their degradation: miR-27 is targeted by both murine cytomegalovirus and herpesvirus saimiri, while the miR-17 family is targeted by human cytomegalovirus. We review what is known about RNA-mediated regulation of miRNA stability and propose 3 potential roles that viral non-coding RNAs might assume to initiate the destruction of a miRNA, acting as "recruiters," "localizers" or "exposers." Whereas the miRNAs (miR-17 and miR-27) appear to be ancient and pre-date the common ancestor of all mammalian herpesviruses, comparative analyses of herpesvirus genomes indicate that the 3 known viral regulators of miRNA each evolved independently, and much more recently. Noting that the anti-viral activity of miRNAs might be countered by a variety of mechanisms, we propose that (i) there has been continual turnover of these mechanisms during herpesvirus evolution, and (ii) there may be many other, as yet undescribed, anti-miRNA activities encoded by other herpesviruses and indeed by viruses from other families.

摘要

其他非编码RNA对小RNA的调控是基因调控系统中普遍存在的一个特征,病毒也可以利用这一特征。在3种不同的疱疹病毒中已有相关例子的描述,其中病毒非编码RNA与高度丰富的细胞(微小RNA)结合,介导其降解:小鼠巨细胞病毒和赛米利疱疹病毒均靶向miR-27,而人巨细胞病毒靶向miR-17家族。我们综述了关于RNA介导的微小RNA稳定性调控的已知信息,并提出病毒非编码RNA可能发挥的3种潜在作用,即作为“招募者”“定位者”或“暴露者”来启动微小RNA的破坏。虽然微小RNA(miR-17和miR-27)似乎较为古老,早于所有哺乳动物疱疹病毒的共同祖先,但疱疹病毒基因组的比较分析表明,已知的3种微小RNA病毒调节因子均是独立进化的,且时间更近。鉴于微小RNA的抗病毒活性可能会被多种机制抵消,我们提出:(i)在疱疹病毒进化过程中,这些机制一直在不断更新;(ii)可能还有许多其他尚未描述的抗微小RNA活性,由其他疱疹病毒乃至其他病毒家族的病毒编码。

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