All About the RNA: Interferon-Stimulated Genes That Interfere With Viral RNA Processes

被引:91
|
作者
Yang, Emily [1 ,2 ]
Li, Melody M. H. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
interferon-stimulated genes; co-factors; viral RNA degradation; translation inhibition; RNA sensing; FINGER ANTIVIRAL PROTEIN; SINGLE-STRANDED RNA; HEPATITIS-B-VIRUS; 2'; 5'-OLIGOADENYLATE SYNTHETASE; NON-SELF; NEGATIVE REGULATOR; MOLECULAR-CLONING; RIG-I; REPLICATION; ISG20;
D O I
10.3389/fimmu.2020.605024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferon (IFN) signaling induces the expression of a wide array of genes, collectively referred to as IFN-stimulated genes (ISGs) that generally function to inhibit viral replication. RNA viruses are frequently targeted by ISGs through recognition of viral replicative intermediates and molecular features associated with viral genomes, or the lack of molecular features associated with host mRNAs. The ISGs reviewed here primarily inhibit viral replication in an RNA-centric manner, working to sense, degrade, or repress expression of viral RNA. This review focuses on dissecting how these ISGs exhibit multiple antiviral mechanisms, often through use of varied co-factors, highlighting the complexity of the type I IFN response. Specifically, these ISGs can mediate antiviral effects through viral RNA degradation, viral translation inhibition, or both. While the OAS/RNase L pathway globally degrades RNA and arrests translation, ISG20 and ZAP employ targeted RNA degradation and translation inhibition to block viral replication. Meanwhile, SHFL targets translation by inhibiting -1 ribosomal frameshifting, which is required by many RNA viruses. Finally, a number of E3 ligases inhibit viral transcription, an attractive antiviral target during the lifecycle of negative-sense RNA viruses which must transcribe their genome prior to translation. Through this review, we aim to provide an updated perspective on how these ISGs work together to form a complex network of antiviral arsenals targeting viral RNA processes.
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页数:18
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