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禽疱疹病毒微小RNA在感染、潜伏和肿瘤发生中的作用。

Roles of avian herpesvirus microRNAs in infection, latency, and oncogenesis.

作者信息

Morgan Robin W, Burnside Joan

机构信息

Department of Animal and Food Sciences, University of Delaware, Newark, DE, USA.

出版信息

Biochim Biophys Acta. 2011 Nov-Dec;1809(11-12):654-9. doi: 10.1016/j.bbagrm.2011.06.001. Epub 2011 Jun 13.

DOI:10.1016/j.bbagrm.2011.06.001
PMID:21683170
Abstract

MicroRNAs have been reported for the avian herpesviruses Marek's disease virus 1 (MDV1; oncogenic), Marek's disease virus 2 (MDV2; non-oncogenic), herpesvirus of turkeys (HVT), and infectious laryngotracheitis virus (ILTV). No obvious phylogenetic relationships exist among the avian herpesvirus microRNAs, but the general genomic locations of microRNA clusters are conserved, with microRNAs being located in the repeat regions of the genomes. In some cases, microRNAs are antisense to open reading frames. Among MDV1 field isolates with different virulence properties, microRNAs are highly conserved, and variations that have been observed lie in putative promoter regions. One cluster of MDV1 microRNAs lies upstream of the meq gene, and this cluster is more highly expressed in tumors caused by an extremely virulent MDV1 isolate compared to tumors caused by a less virulent isolate. Several of the avian herpesvirus microRNAs are orthologs of microRNAs in other species. For example, mdv1-miR-M4 shares a seed sequence with gga-miR-155 (also shared with Kaposi sarcoma herpesvirus (KSHV) kshv-miR-K12), mdv2-miR-M21 shares a seed with miR-29b, and hvt-miR-H14 shares a seed sequence with miR-221. Functional analyses of avian herpesvirus microRNAs include a variety of in vitro assays to demonstrate potential function as well as the use of mutants that can exploit the ability to assess phenotypes experimentally in the natural host. This article is part of a Special Issue entitled:MicroRNA's in viral gene regulation.

摘要

已有报道称,在禽疱疹病毒中发现了微小RNA,包括马立克氏病病毒1型(MDV1;致癌性)、马立克氏病病毒2型(MDV2;非致癌性)、火鸡疱疹病毒(HVT)和传染性喉气管炎病毒(ILTV)。禽疱疹病毒微小RNA之间不存在明显的系统发育关系,但微小RNA簇的一般基因组位置是保守的,微小RNA位于基因组的重复区域。在某些情况下,微小RNA与开放阅读框呈反义关系。在具有不同毒力特性的MDV1田间分离株中,微小RNA高度保守,观察到的变异位于假定的启动子区域。MDV1微小RNA的一个簇位于meq基因上游,与由低毒力分离株引起的肿瘤相比,该簇在由极毒力MDV1分离株引起的肿瘤中表达更高。几种禽疱疹病毒微小RNA是其他物种微小RNA的直系同源物。例如,mdv1-miR-M4与gga-miR-155共享种子序列(也与卡波西肉瘤疱疹病毒(KSHV)的kshv-miR-K12共享),mdv2-miR-M21与miR-29b共享种子序列,hvt-miR-H14与miR-221共享种子序列。禽疱疹病毒微小RNA的功能分析包括各种体外试验以证明其潜在功能,以及使用能够利用在天然宿主中通过实验评估表型的能力的突变体。本文是名为《病毒基因调控中的微小RNA》特刊的一部分。

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