Department of Microbiology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA; Department of Medicine, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA.
J Mol Biol. 2014 Mar 20;426(6):1265-84. doi: 10.1016/j.jmb.2013.12.005. Epub 2013 Dec 12.
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.
三基序蛋白(TRIM)参与多种细胞功能,包括抗病毒活性。到目前为止的研究表明,TRIM 的抗病毒活性在很大程度上依赖于其作为 E3-泛素连接酶的功能。大量的 TRIM 家族成员被证明介导先天免疫细胞信号转导和随后的细胞因子诱导。此外,一部分 TRIM 通过直接靶向病毒蛋白来限制病毒复制。尽管近年来关于 TRIM E3-泛素连接酶的细胞作用的研究迅速增加,但它们的分子作用和多功能性的许多方面仍不清楚。许多 TRIM 的抗病毒功能似乎是由特定的亚型、亚细胞定位和细胞类型特异性背景赋予的。在这里,我们回顾了 TRIM 抗病毒功能的最新发现、当前的局限性和对未来研究的展望。