MRC Protein Phosphorylation and Ubiquitylation Unit, Sir James Black Centre, University of Dundee, Dundee DD1 5EH, Scotland, United Kingdom.
J Biol Chem. 2013 Aug 23;288(34):24569-80. doi: 10.1074/jbc.M113.479550. Epub 2013 Jul 11.
Double-stranded (ds) RNA of viral origin, a ligand for Melanoma Differentiation-associated gene 5 (MDA5) and Toll-Like Receptor 3 (TLR3), induces the TANK-Binding Kinase 1 (TBK1)-dependent phosphorylation and activation of Interferon Regulatory Factor 3 (IRF3) and the E3 ubiquitin ligase Pellino1, which are required for interferon β (IFNβ) gene transcription. Here, we report that Pellino1 interacts with the transcription factor Deformed Epidermal Autoregulatory Factor 1 (DEAF1). The interaction is independent of the E3 ligase activity of Pellino1, but weakened by the phosphorylation of Pellino1. We show that DEAF1 binds to the IFNβ promoter and to IRF3 and IRF7, that it is required for the transcription of the IFNβ gene and IFNβ secretion in MEFs infected with Sendai virus or transfected with poly(I:C). DEAF1 is also needed for TLR3-dependent IFNβ production. Taken together, our results identify DEAF1 as a novel component of the signal transduction network by which dsRNA of viral origin stimulates IFNβ production.
病毒来源的双链 RNA(dsRNA)是黑色素瘤分化相关基因 5(MDA5)和 Toll 样受体 3(TLR3)的配体,可诱导 TANK 结合激酶 1(TBK1)依赖性磷酸化和干扰素调节因子 3(IRF3)和 E3 泛素连接酶 Pellino1 的激活,这对于干扰素 β(IFNβ)基因转录是必需的。在这里,我们报告 Pellino1 与转录因子畸形表皮自动调节因子 1(DEAF1)相互作用。这种相互作用不依赖于 Pellino1 的 E3 连接酶活性,但被 Pellino1 的磷酸化削弱。我们表明,DEAF1 结合 IFNβ 启动子以及 IRF3 和 IRF7,它是 MEFs 感染 Sendai 病毒或转染 poly(I:C)时 IFNβ 基因转录和 IFNβ 分泌所必需的。DEAF1 也需要 TLR3 依赖性 IFNβ 的产生。总之,我们的结果表明 DEAF1 是病毒来源的 dsRNA 刺激 IFNβ 产生的信号转导网络的一个新组成部分。