TRIM Proteins and Their Roles in Antiviral Host Defenses

被引:253
作者
van Gent, Michiel [1 ]
Sparrer, Konstantin M. J. [1 ]
Gack, Michaela U. [1 ]
机构
[1] Univ Chicago, Dept Microbiol, Chicago, IL 60637 USA
来源
ANNUAL REVIEW OF VIROLOGY, VOL 5 | 2018年 / 5卷
基金
美国国家卫生研究院;
关键词
TRIM protein; antiviral restriction; innate immunity; virus infection; interferon; E3 UBIQUITIN LIGASE; NF-KAPPA-B; INTERFERON-STIMULATED GENES; INNATE IMMUNE-RESPONSE; IFN-BETA PRODUCTION; RIG-I; NEGATIVE REGULATOR; INFLUENZA-A; FAMILY PROTEINS; VIRUS-INFECTION;
D O I
10.1146/annurev-virology-092917-043323
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tripartite motif (TRIM) proteins are a versatile family of ubiquitin E3 ligases involved in a multitude of cellular processes. Studies in recent years have demonstrated that many TRIM proteins play central roles in the host defense against viral infection. While some TRIM proteins directly antagonize distinct steps in the viral life cycle, others regulate signal transduction pathways induced by innate immune sensors, thereby modulating antiviral cytokine responses. Furthermore, TRIM proteins have been implicated in virus-induced autophagy and autophagy-mediated viral clearance. Given the important role of TRIM proteins in antiviral restriction, it is not surprising that several viruses have evolved effective maneuvers to neutralize the antiviral action of specific TRIM proteins. Here, we describe the major antiviral mechanisms of TRIM proteins as well as viral strategies to escape TRIM-mediated host immunity.
引用
收藏
页码:385 / 405
页数:21
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