Key Laboratory for Experimental Teratology of the Ministry of Education & Department of Immunology, Shandong University School of Medicine, Jinan, Shandong, China.
J Virol. 2013 Apr;87(8):4507-15. doi: 10.1128/JVI.00031-13. Epub 2013 Feb 6.
Protein ubiquitination plays an essential role in the regulation of retinoic acid-inducible gene I (RIG-I) activation and the antiviral immune response. However, the function of the opposite process of deubiquitination in RIG-I activation remains elusive. In this study, we have identified the deubiquitinating enzyme ubiquitin-specific protease 4 (USP4) as a new regulator for RIG-I activation through deubiquitination and stabilization of RIG-I. USP4 expression was attenuated after virus-induced RIG-I activation. Overexpression of USP4 significantly enhanced RIG-I protein expression and RIG-I-triggered beta interferon (IFN-β) signaling and, at the same time, inhibited vesicular stomatitis virus (VSV) replication. Small interfering RNA (siRNA) knockdown of USP4 expression had an opposite effect. Furthermore, USP4 was found to interact with RIG-I and remove K48-linked polyubiquitination chains from RIG-I. Therefore, we identified USP4 as a new positive regulator for RIG-I that acts through deubiquitinating K48-linked ubiquitin chains and stabilizing RIG-I.
蛋白泛素化在调控视黄酸诱导基因 I(RIG-I)激活和抗病毒免疫反应中起着至关重要的作用。然而,RIG-I 激活过程中去泛素化的相反作用的功能仍然难以捉摸。在这项研究中,我们通过去泛素化和稳定 RIG-I,鉴定了泛素特异性蛋白酶 4(USP4)作为 RIG-I 激活的新调节剂。病毒诱导的 RIG-I 激活后,USP4 的表达减弱。USP4 的过表达显著增强了 RIG-I 蛋白表达和 RIG-I 触发的β干扰素(IFN-β)信号通路,同时抑制了水疱性口炎病毒(VSV)的复制。USP4 表达的小干扰 RNA(siRNA)敲低则产生相反的效果。此外,发现 USP4 与 RIG-I 相互作用,并从 RIG-I 上去除 K48 连接的多泛素链。因此,我们鉴定了 USP4 作为一种新的 RIG-I 正向调节剂,通过去泛素化 K48 连接的泛素链和稳定 RIG-I 发挥作用。