An "Old" protein with a new story: Coronavirus endoribonuclease is important for evading host antiviral defenses

被引:108
作者
Deng, Xufang [1 ]
Baker, Susan C. [1 ]
机构
[1] Loyola Univ Chicago, Stritch Sch Med, Dept Microbiol & Immunol, Maywood, IL 60153 USA
基金
美国国家卫生研究院;
关键词
Coronavirus; Nsp15; Endoribonuclease; Double-stranded RNA; Interferon; Host recognition; Antiviral defense; MURINE CORONAVIRUS; CRYSTAL-STRUCTURE; SARS-CORONAVIRUS; NSP15; ENDORIBONUCLEASE; RNA-SYNTHESIS; VIRUS; PORCINE; ANTAGONISM; IDENTIFICATION; ACTIVATION;
D O I
10.1016/j.virol.2017.12.024
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Here we review the evolving story of the coronavirus endoribonuclease (EndoU). Coronavirus EndoU is encoded within the sequence of nonstructural protein (nsp) 15, which was initially identified as a component of the viral replication complex. Biochemical and structural studies revealed the enzymatic nature of nsp15/EndoU, which was postulated to be essential for the unique replication cycle of viruses in the order Nidovirales. However, the role of nsp15 in coronavirus replication was enigmatic as EndoU-deficient coronaviruses were viable and replicated to near wild-type virus levels in fibroblast cells. A breakthrough in our understanding of the role of EndoU was revealed in recent studies, which showed that EndoU mediates the evasion of viral double-stranded RNA recognition by host sensors in macrophages. This new discovery of nsp15/EndoU function leads to new opportunities for investigating how a viral EndoU contributes to pathogenesis and exploiting this enzyme for therapeutics and vaccine design against pathogenic coronaviruses.
引用
收藏
页码:157 / 163
页数:7
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