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动物细胞质RNA病毒与细胞核相互作用以促进复制。

The interaction of animal cytoplasmic RNA viruses with the nucleus to facilitate replication.

作者信息

Hiscox Julian A

机构信息

School of Biochemistry and Molecular Biology, University of Leeds, LS2 9JT Leeds, UK.

出版信息

Virus Res. 2003 Sep;95(1-2):13-22. doi: 10.1016/s0168-1702(03)00160-6.

Abstract

A number of positive and negative strand RNA viruses whose primary site of replication is the cytoplasm use the nucleus and/or nuclear components in order to facilitate their replicative processes and alter host cell function. The nucleus itself is divided into a number of different sub-domains including structures such as the nucleolus. Many of the nuclear proteins that localise to these domains are involved in RNA processing, and because of their limited coding capacity, it may be necessary for RNA viruses to sequester such cellular factors in order to facilitate the replication, transcription and translation of their genomes. Amongst the best-studied examples of this are the picornaviruses, whose infection results in the redistribution of nuclear proteins to the cytoplasm and their interaction with the internal ribosome entry site (IRES) to facilitate translation of the picornavirus polyprotein. Examples can be found of other positive and also negative strand RNA virus proteins that localise to the nucleus and sub-domains (especially the nucleolus) during virus infection, and several localisation motifs have been defined. Apart from sequestering nuclear proteins for a role in replication, such viruses may also target the nucleus to disrupt nuclear functions and to inhibit antiviral responses.

摘要

许多以细胞质为主要复制位点的正链和负链RNA病毒会利用细胞核和/或核成分来促进其复制过程并改变宿主细胞功能。细胞核本身被分为多个不同的亚结构域,包括核仁等结构。许多定位于这些结构域的核蛋白都参与RNA加工,并且由于RNA病毒的编码能力有限,它们可能需要隔离这些细胞因子,以促进其基因组的复制、转录和翻译。其中研究得最透彻的例子是小RNA病毒,其感染会导致核蛋白重新分布到细胞质中,并与内部核糖体进入位点(IRES)相互作用,以促进小RNA病毒多聚蛋白的翻译。在病毒感染期间,其他正链和负链RNA病毒蛋白定位于细胞核和亚结构域(尤其是核仁)的例子也有发现,并且已经确定了几种定位基序。除了隔离核蛋白以参与复制外,这类病毒还可能靶向细胞核以破坏核功能并抑制抗病毒反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b275/7125749/a7ec5b7fe81b/gr1.jpg

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