Boss Isaac W, Renne Rolf
Department of Molecular Genetics and Microbiology, University of Florida, Gainsville, FL, USA.
Biochim Biophys Acta. 2011 Nov-Dec;1809(11-12):708-14. doi: 10.1016/j.bbagrm.2011.06.012. Epub 2011 Jul 5.
Viral miRNAs, ~22nt RNA molecules which post-transcriptionally regulate gene expression, are emerging as important tools in immune evasion. Viral infection is a complex process that requires immune evasion in order to establish persistent life-long infection of the host. During this process viruses express both protein-coding and non-coding genes, which help to modulate the cellular environment making it more favorable for infection. In the last decade, it was uncovered that DNA viruses express a diverse and abundant pool of small non-coding RNA molecules, called microRNAs (miRNAs). These virally encoded miRNAs are non-immunogenic and therefore are important tools used to evade both innate and adaptive immune responses. This review aims to summarize our current knowledge of herpesvirus- and polyomavirus-encoded miRNAs, and how they contribute to immune evasion by targeting viral and/or host cellular genes. This article is part of a Special Issue entitled: MicroRNAs in viral gene regulation.
病毒微小RNA(miRNA)是一类约22个核苷酸的RNA分子,可在转录后水平调节基因表达,正逐渐成为免疫逃逸中的重要工具。病毒感染是一个复杂的过程,为了在宿主体内建立终身持续性感染,需要进行免疫逃逸。在此过程中,病毒会表达蛋白质编码基因和非编码基因,这些基因有助于调节细胞环境,使其更有利于感染。在过去十年中,人们发现DNA病毒会表达多种多样且丰富的小非编码RNA分子,即微小RNA(miRNA)。这些病毒编码的miRNA具有非免疫原性,因此是用于逃避固有免疫和适应性免疫反应的重要工具。本综述旨在总结我们目前对疱疹病毒和多瘤病毒编码的miRNA的了解,以及它们如何通过靶向病毒和/或宿主细胞基因来促进免疫逃逸。本文是名为“病毒基因调控中的微小RNA”的特刊的一部分。