State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, 1 Beichen West Road, Chaoyang District, Beijing 100101, China.
State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, 1 Beichen West Road, Chaoyang District, Beijing 100101, China.
Nat Commun. 2016 Jun 9;7:11848. doi: 10.1038/ncomms11848.
Retinoic acid-inducible gene I (RIG-I) plays important roles in pathogen recognition and antiviral signalling transduction. Here we show that syndecan-4 (SDC4) is a RIG-I-interacting partner identified in a yeast two-hybrid screen. We find that SDC4 negatively regulates the RIG-I-mediated antiviral signalling in a feedback-loop control manner. The genetic evidence obtained by using knockout mice further emphasizes this biological role of SDC4 in antiviral signalling. Mechanistically, we show that SDC4 interacts with both RIG-I and deubiquitinase CYLD via its carboxyl-terminal intracellular region. SDC4 likely promotes redistribution of RIG-I and CYLD in a perinuclear pattern post viral infection, and thus enhances the RIG-I-CYLD interaction and potentiates the K63-linked deubiquitination of RIG-I. Collectively, our findings uncover a mechanism by which SDC4 antagonizes the activation of RIG-I in a CYLD-mediated deubiquitination-dependent process, thereby balancing antiviral signalling to avoid deleterious effects on host cells.
视黄酸诱导基因 I(RIG-I)在病原体识别和抗病毒信号转导中发挥重要作用。在这里,我们发现硫酸乙酰肝素蛋白聚糖-4(SDC4)是通过酵母双杂交筛选鉴定出的 RIG-I 相互作用伙伴。我们发现 SDC4 以负反馈调节方式负调控 RIG-I 介导的抗病毒信号。通过使用基因敲除小鼠获得的遗传证据进一步强调了 SDC4 在抗病毒信号中的这种生物学作用。从机制上讲,我们表明 SDC4 通过其羧基末端细胞内区域与 RIG-I 和去泛素化酶 CYLD 相互作用。SDC4 可能在病毒感染后促进 RIG-I 和 CYLD 在核周模式下的重新分布,从而增强 RIG-I-CYLD 相互作用并增强 RIG-I 的 K63 连接去泛素化。总之,我们的发现揭示了 SDC4 通过 CYLD 介导的去泛素化依赖过程拮抗 RIG-I 激活的机制,从而平衡抗病毒信号,避免对宿主细胞产生有害影响。