Dastur Anahita, Beaudenon Sylvie, Kelley Melissa, Krug Robert M, Huibregtse Jon M
Institute for Cellular and Molecular Biology, Section of Molecular Genetics and Microbiology, The University of Texas at Austin, 78712, USA.
J Biol Chem. 2006 Feb 17;281(7):4334-8. doi: 10.1074/jbc.M512830200. Epub 2005 Dec 28.
ISG15 is an interferon (IFN)-alpha/beta-induced ubiquitin-like protein that is conjugated to cellular proteins during innate immune responses to viral and bacterial infections. A recent proteomics study identified 158 human proteins targeted for ISG15 conjugation, including the ISG15 E1 and E2 enzymes (Ube1L and UbcH8, respectively) and a HECT E3 enzyme, Herc5. Like the genes encoding Ube1L and UbcH8, expression of Herc5 was also induced by IFN-beta, suggesting that Herc5 might be a component of the ISG15 conjugation system. Consistent with this, small interfering RNAs targeting Herc5 had a dramatic effect on overall ISG15 conjugation in human cells, abrogating conjugation to the vast majority of ISG15 target proteins in vivo. In addition, co-transfection of plasmids expressing ISG15, Ube1L, UbcH8, and Herc5 resulted in robust ISG15 conjugation in non-IFN-treated cells, while the active-site cysteine mutant of Herc5 or a mutant lacking the RCC1 repeat region did not support ISG15 conjugation. These results demonstrate that Herc5 is required for conjugation of ISG15 to a broad spectrum of target proteins in human cells.
ISG15是一种干扰素(IFN)-α/β诱导的类泛素蛋白,在对病毒和细菌感染的先天免疫反应过程中与细胞蛋白结合。最近的一项蛋白质组学研究鉴定出158种被ISG15结合的人类蛋白,包括ISG15 E1和E2酶(分别为Ube1L和UbcH8)以及一种HECT E3酶Herc5。与编码Ube1L和UbcH8的基因一样,Herc5的表达也受到IFN-β的诱导,这表明Herc5可能是ISG15结合系统的一个组成部分。与此一致的是,靶向Herc5的小干扰RNA对人类细胞中的整体ISG15结合有显著影响,在体内消除了与绝大多数ISG15靶蛋白的结合。此外,共转染表达ISG15、Ube1L、UbcH8和Herc5的质粒在未用IFN处理的细胞中导致了强烈的ISG15结合,而Herc5的活性位点半胱氨酸突变体或缺乏RCC1重复区域的突变体则不支持ISG15结合。这些结果表明,Herc5是人类细胞中ISG15与广泛靶蛋白结合所必需的。