TRIMmunity: The Roles of the TRIM E3-Ubiquitin Ligase Family in Innate Antiviral Immunity

被引:290
作者
Rajsbaum, Ricardo [1 ,2 ]
Garcia-Sastre, Adolfo [1 ,2 ,3 ]
Versteeg, Gijs A. [4 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Global Hlth & Emerging Pathogens Inst, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA
[4] Univ Vienna, Max F Perutz Labs, A-1030 Vienna, Austria
关键词
tripartite motif; E3-ubiquitin ligase; innate immunity; restriction factors; antiviral response; NF-KAPPA-B; PROMYELOCYTIC LEUKEMIA PROTEIN; E3 UBIQUITIN LIGASE; DEPENDENT CYTOKINE EXPRESSION; TRIPARTITE MOTIF PROTEINS; IFN-BETA PRODUCTION; RETROVIRAL RESTRICTION; RING-FINGER; TRIM5-ALPHA RESTRICTION; REVERSE TRANSCRIPTION;
D O I
10.1016/j.jmb.2013.12.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tripartite motif (TRIM) proteins have been implicated in multiple cellular functions, including antiviral activity. Research efforts so far indicate that the antiviral activity of TRIMs relies, for the most part, on their function as E3-ubiquitin ligases. A substantial number of the TRIM family members have been demonstrated to mediate innate immune cell signal transduction and subsequent cytokine induction. In addition, a subset of TRIMs has been shown to restrict viral replication by directly targeting viral proteins. Although the body of work on the cellular roles of TRIM E3-ubiquitin ligases has rapidly grown over the last years, many aspects of their molecular workings and multi-functionality remain unclear. The antiviral function of many TRIMs seems to be conferred by specific isoforms, by sub-cellular localization and in cell-type-specific contexts. Here we review recent findings on TRIM antiviral functions, current limitations and an outlook for future research. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1265 / 1284
页数:20
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