Molecular mechanisms of coronavirus RNA capping and methylation

被引:131
作者
Chen, Yu [1 ]
Guo, Deyin [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430070, Peoples R China
关键词
coronavirus; RNA capping; triphosphatase; guanylyltransferase; methyltransferase; cap structure; methylation; RESPIRATORY SYNDROME CORONAVIRUS; EUKARYOTIC MESSENGER-RNAS; SARS-CORONAVIRUS; RIG-I; FUNCTIONAL-ANALYSIS; VIRUS-REPLICATION; VACCINIA VIRUS; CAP GUANINE-N7-METHYLTRANSFERASE; METHYLTRANSFERASE INHIBITOR; CANDIDA-ALBICANS;
D O I
10.1007/s12250-016-3726-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:3 / 11
页数:9
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