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冠状病毒RNA加帽和甲基化的分子机制。

Molecular mechanisms of coronavirus RNA capping and methylation.

作者信息

Chen Yu, Guo Deyin

机构信息

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430070, China.

出版信息

Virol Sin. 2016 Feb;31(1):3-11. doi: 10.1007/s12250-016-3726-4. Epub 2016 Feb 2.

Abstract

The 5'-cap structures of eukaryotic mRNAs are important for RNA stability, pre-mRNA splicing, mRNA export, and protein translation. Many viruses have evolved mechanisms for generating their own cap structures with methylation at the N7 position of the capped guanine and the ribose 2'-Oposition of the first nucleotide, which help viral RNAs escape recognition by the host innate immune system. The RNA genomes of coronavirus were identified to have 5'-caps in the early 1980s. However, for decades the RNA capping mechanisms of coronaviruses remained unknown. Since 2003, the outbreak of severe acute respiratory syndrome coronavirus has drawn increased attention and stimulated numerous studies on the molecular virology of coronaviruses. Here, we review the current understanding of the mechanisms adopted by coronaviruses to produce the 5'-cap structure and methylation modification of viral genomic RNAs.

摘要

真核生物mRNA的5'-帽结构对于RNA稳定性、前体mRNA剪接、mRNA输出和蛋白质翻译至关重要。许多病毒已经进化出机制来产生它们自己的帽结构,即在带帽鸟嘌呤的N7位置和第一个核苷酸的核糖2'-O位置进行甲基化,这有助于病毒RNA逃避宿主先天免疫系统的识别。冠状病毒的RNA基因组在20世纪80年代初被鉴定为具有5'-帽。然而,几十年来冠状病毒的RNA加帽机制一直未知。自2003年以来,严重急性呼吸综合征冠状病毒的爆发引起了越来越多的关注,并激发了对冠状病毒分子病毒学的大量研究。在此,我们综述了目前对冠状病毒产生5'-帽结构以及病毒基因组RNA甲基化修饰所采用机制的理解。

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