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本文引用的文献

1
An Epstein-Barr virus-encoded microRNA targets PUMA to promote host cell survival.一种爱泼斯坦-巴尔病毒编码的微小RNA靶向PUMA以促进宿主细胞存活。
J Exp Med. 2008 Oct 27;205(11):2551-60. doi: 10.1084/jem.20072581. Epub 2008 Oct 6.
2
The HIV-2 TAR RNA domain as a potential source of viral-encoded miRNA. A reconnaissance study.作为病毒编码微小RNA潜在来源的HIV-2 TAR RNA结构域:一项初步研究。
Nucleic Acids Symp Ser (Oxf). 2008(52):511-2. doi: 10.1093/nass/nrn259.
3
miR-122 targets an anti-apoptotic gene, Bcl-w, in human hepatocellular carcinoma cell lines.在人肝癌细胞系中,miR-122靶向一个抗凋亡基因Bcl-w。
Biochem Biophys Res Commun. 2008 Oct 24;375(3):315-20. doi: 10.1016/j.bbrc.2008.07.154. Epub 2008 Aug 8.
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Evolutionarily conserved function of a viral microRNA.病毒微小RNA的进化保守功能
J Virol. 2008 Oct;82(20):9823-8. doi: 10.1128/JVI.01144-08. Epub 2008 Aug 6.
5
An acutely and latently expressed herpes simplex virus 2 viral microRNA inhibits expression of ICP34.5, a viral neurovirulence factor.一种急性和潜伏表达的单纯疱疹病毒2型病毒微小RNA抑制病毒神经毒力因子ICP34.5的表达。
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Manifestations of human cytomegalovirus infection: proposed mechanisms of acute and chronic disease.人类巨细胞病毒感染的表现:急性和慢性疾病的潜在机制
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Aspects of human cytomegalovirus latency and reactivation.人类巨细胞病毒潜伏与再激活的各个方面。
Curr Top Microbiol Immunol. 2008;325:297-313. doi: 10.1007/978-3-540-77349-8_17.
8
Epstein-Barr virus BART microRNAs are produced from a large intron prior to splicing.爱泼斯坦-巴尔病毒BART微小RNA是在剪接之前从一个大内含子产生的。
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9
MicroRNAs expressed by herpes simplex virus 1 during latent infection regulate viral mRNAs.单纯疱疹病毒1型在潜伏感染期间表达的微小RNA可调控病毒mRNA。
Nature. 2008 Aug 7;454(7205):780-3. doi: 10.1038/nature07103. Epub 2008 Jul 2.
10
Capped small RNAs and MOV10 in human hepatitis delta virus replication.人丁型肝炎病毒复制中的帽状小RNA与MOV10
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病毒感染细胞中微小RNA和非编码RNA的当前知识。

Current knowledge of MicroRNAs and noncoding RNAs in virus-infected cells.

作者信息

Ouellet Dominique L, Provost Patrick

机构信息

Centre de Recherche en Rhumatologie et Immunologie, CHUL Research Center/CHUQ, Quebec, QC, Canada.

出版信息

Methods Mol Biol. 2010;623:35-65. doi: 10.1007/978-1-60761-588-0_3.

DOI:10.1007/978-1-60761-588-0_3
PMID:20217543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2906133/
Abstract

Within the past few years, microRNAs (miRNAs) and other noncoding RNAs (ncRNAs) have emerged as elements with critically high importance in posttranscriptional control of cellular and, more recently, viral processes. Endogenously produced by a component of the miRNA-guided RNA silencing machinery known as Dicer, miRNAs are known to control messenger RNA (mRNA) translation through recognition of specific binding sites usually located in their 3' untranslated region. Recent evidences indicate that the host miRNA pathway may represent an adapted antiviral defense mechanism that can act either by direct miRNA-mediated modulation of viral gene expression or through recognition and inactivation of structured viral RNA species by the protein components of the RNA silencing machinery such as Dicer. This latter process, however, is a double-edge sword, as it may yield viral miRNAs exerting gene regulatory properties on both host and viral mRNAs. Our knowledge of the interaction between viruses and host RNA silencing machineries, and how this influences the course of infection, is becoming increasingly complex. This chapter aims to summarize our current knowledge about viral miRNAs/ncRNAs and their targets, as well as cellular miRNAs that are modulated by viruses upon infection.

摘要

在过去几年中,微小RNA(miRNA)和其他非编码RNA(ncRNA)已成为在细胞转录后调控以及最近在病毒过程中具有至关重要意义的元素。miRNA由一种称为Dicer的miRNA引导的RNA沉默机制的成分内源性产生,已知其通过识别通常位于其3'非翻译区的特定结合位点来控制信使RNA(mRNA)的翻译。最近的证据表明,宿主miRNA途径可能代表一种适应性抗病毒防御机制,其可以通过直接的miRNA介导的病毒基因表达调节或通过RNA沉默机制(如Dicer)的蛋白质成分识别和灭活结构化病毒RNA种类来发挥作用。然而,后一种过程是一把双刃剑,因为它可能产生对宿主和病毒mRNA都具有基因调控特性的病毒miRNA。我们对病毒与宿主RNA沉默机制之间相互作用以及这如何影响感染过程的了解正变得越来越复杂。本章旨在总结我们目前关于病毒miRNA/ncRNA及其靶标的知识,以及感染后受病毒调节的细胞miRNA。