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本文引用的文献

1
Architecture and biogenesis of plus-strand RNA virus replication factories.正链RNA病毒复制工厂的结构与生物发生
World J Virol. 2013 May 12;2(2):32-48. doi: 10.5501/wjv.v2.i2.32.
2
"Megavirales", a proposed new order for eukaryotic nucleocytoplasmic large DNA viruses.“巨型病毒目”,一个新提议的真核核质大 DNA 病毒的目。
Arch Virol. 2013 Dec;158(12):2517-21. doi: 10.1007/s00705-013-1768-6. Epub 2013 Jun 29.
3
The interaction of the cellular export adaptor protein Aly/REF with ICP27 contributes to the efficiency of herpes simplex virus 1 mRNA export.细胞输出衔接蛋白 Aly/REF 与 ICP27 的相互作用有助于单纯疱疹病毒 1 mRNA 的输出效率。
J Virol. 2013 Jul;87(13):7210-7. doi: 10.1128/JVI.00738-13. Epub 2013 May 1.
4
African swine fever virus organelle rearrangements.非洲猪瘟病毒细胞器重排。
Virus Res. 2013 Apr;173(1):76-86. doi: 10.1016/j.virusres.2012.12.014. Epub 2013 Jan 3.
5
Virus-induced aggregates in infected cells.病毒感染细胞中诱导产生的聚集物。
Viruses. 2012 Oct 17;4(10):2218-32. doi: 10.3390/v4102218.
6
African swine fever virus controls the host transcription and cellular machinery of protein synthesis.非洲猪瘟病毒控制宿主转录和细胞蛋白质合成机制。
Virus Res. 2013 Apr;173(1):58-75. doi: 10.1016/j.virusres.2012.10.025. Epub 2012 Nov 12.
7
RNAi screening reveals proteasome- and Cullin3-dependent stages in vaccinia virus infection.RNAi 筛选揭示了痘病毒感染过程中依赖于蛋白酶体和 Cullin3 的阶段。
Cell Rep. 2012 Oct 25;2(4):1036-47. doi: 10.1016/j.celrep.2012.09.003. Epub 2012 Oct 19.
8
African swine fever virus morphogenesis.非洲猪瘟病毒形态发生。
Virus Res. 2013 Apr;173(1):29-41. doi: 10.1016/j.virusres.2012.09.016. Epub 2012 Oct 8.
9
Design stars: how small DNA viruses remodel the host nucleus.设计之星:小型DNA病毒如何重塑宿主细胞核
Future Virol. 2012 May 1;7(5):445-459. doi: 10.2217/FVL.12.38.
10
Adenovirus regulates sumoylation of Mre11-Rad50-Nbs1 components through a paralog-specific mechanism.腺病毒通过一种蛋白家族特异性机制调控 Mre11-Rad50-Nbs1 复合物的 SUMO 化修饰。
J Virol. 2012 Sep;86(18):9656-65. doi: 10.1128/JVI.01273-12. Epub 2012 Jun 27.

DNA 病毒复制区室。

DNA virus replication compartments.

机构信息

Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Hamburg, Germany.

出版信息

J Virol. 2014 Feb;88(3):1404-20. doi: 10.1128/JVI.02046-13. Epub 2013 Nov 20.

DOI:10.1128/JVI.02046-13
PMID:24257611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3911613/
Abstract

Viruses employ a variety of strategies to usurp and control cellular activities through the orchestrated recruitment of macromolecules to specific cytoplasmic or nuclear compartments. Formation of such specialized virus-induced cellular microenvironments, which have been termed viroplasms, virus factories, or virus replication centers, complexes, or compartments, depends on molecular interactions between viral and cellular factors that participate in viral genome expression and replication and are in some cases associated with sites of virion assembly. These virus-induced compartments function not only to recruit and concentrate factors required for essential steps of the viral replication cycle but also to control the cellular mechanisms of antiviral defense. In this review, we summarize characteristic features of viral replication compartments from different virus families and discuss similarities in the viral and cellular activities that are associated with their assembly and the functions they facilitate for viral replication.

摘要

病毒采用多种策略,通过将大分子有组织地募集到特定的细胞质或核区室,从而篡夺和控制细胞活动。形成这种专门的病毒诱导的细胞微环境,被称为类病毒体、病毒工厂或病毒复制中心、复合物或区室,取决于参与病毒基因组表达和复制的病毒和细胞因子之间的分子相互作用,在某些情况下,还与病毒体组装的部位相关。这些病毒诱导的区室不仅用于募集和浓缩病毒复制周期必需步骤所需的因子,而且还用于控制抗病毒防御的细胞机制。在这篇综述中,我们总结了不同病毒科的病毒复制区室的特征,并讨论了与它们的组装以及它们为病毒复制提供便利的功能相关的病毒和细胞活动的相似性。