Virology Group, International Centre for Genetic Engineering & Biotechnology, New Delhi, 110067, India.
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Antiviral Res. 2020 Apr;176:104747. doi: 10.1016/j.antiviral.2020.104747. Epub 2020 Feb 21.
Influenza virus non-structural protein 1 (NS1) counteracts host antiviral innate immune responses by inhibiting Retinoic acid inducible gene-I (RIG-I) activation. However, whether NS1 also specifically regulates RIG-I transcription is unknown. Here, we identify a CCAAT/Enhancer Binding Protein beta (C/EBPβ) binding site in the RIG-I promoter as a repressor element, and show that NS1 promotes C/EBPβ phosphorylation and its recruitment to the RIG-I promoter as a C/EBPβ/NS1 complex. C/EBPβ overexpression and siRNA knockdown in human lung epithelial cells resulted in suppression and activation of RIG-I expression respectively, implying a negative regulatory role of C/EBPβ. Further, C/EBPβ phosphorylation, its interaction with NS1 and occupancy at the RIG-I promoter was associated with RIG-I transcriptional inhibition. These findings provide an important insight into the molecular mechanism by which influenza NS1 commandeers RIG-I transcriptional regulation and suppresses host antiviral responses.
流感病毒非结构蛋白 1(NS1)通过抑制视黄酸诱导基因-I(RIG-I)的激活来拮抗宿主抗病毒固有免疫反应。然而,NS1 是否也特异性调节 RIG-I 转录尚不清楚。在这里,我们在 RIG-I 启动子中鉴定出一个 CCAAT/增强子结合蛋白β(C/EBPβ)结合位点作为一个抑制元件,并表明 NS1 促进 C/EBPβ 的磷酸化及其作为 C/EBPβ/NS1 复合物募集到 RIG-I 启动子。在人肺上皮细胞中过表达和 siRNA 敲低 C/EBPβ 分别导致 RIG-I 表达的抑制和激活,暗示 C/EBPβ 发挥负调控作用。此外,C/EBPβ 的磷酸化、与 NS1 的相互作用以及在 RIG-I 启动子上的占有率与 RIG-I 转录抑制相关。这些发现为流感 NS1 利用 RIG-I 转录调控并抑制宿主抗病毒反应的分子机制提供了重要的见解。