Li Shun, Lu Long-Feng, Wang Zhao-Xi, Chen Dan-Dan, Zhang Yong-An
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Fish Shellfish Immunol. 2016 Oct;57:262-268. doi: 10.1016/j.fsi.2016.08.059. Epub 2016 Aug 28.
Interferon (IFN) regulatory factors (IRF) are the crucial transcription factors for IFN expression, leading host cell response to viral infection. In mammals, only IRF6 is unaffected by IFN expression in the IRF family; however, in fish, a lower vertebrate, whether IRF6 is related to IFN regulation is unclear. In this study, we identified that zebrafish IRF6 was a positive regulator of IFN transcription and could be phosphorylated by both MyD88 and TBK1. First, the transcript level of cellular irf6 was upregulated by treatment with poly I:C (a mimic of viral RNAs), indicating IRF6 might be involved in the process of host cell response to viruses. Overexpression of IRF6 could upregulate IFN promoter activity significantly, meaning IRF6 is a positive regulator of IFN transcription. Subsequently, at the protein regulation level and in the interaction relationship, IRF6 was phosphorylated by and associated with both MyD88 and TBK1. In addition, overexpression of IRF6 activated the transcription of isg15, rig-i and mavs of host cells; meanwhile, the transcripts of p, m and n genes of SVCV were significantly declined in IRF6-overexpressing cells. Taken together, our data demonstrate that fish IRF6 is distinguished from the homolog of mammals by being a positive regulator of IFN transcription and phosphorylated by MyD88 and TBK1, suggesting that differences in the IRF6 regulation pattern exist between lower and higher vertebrates.
干扰素(IFN)调节因子(IRF)是IFN表达的关键转录因子,可引导宿主细胞对病毒感染作出反应。在哺乳动物中,IRF家族中只有IRF6不受IFN表达的影响;然而,在鱼类(一种低等脊椎动物)中,IRF6是否与IFN调节有关尚不清楚。在本研究中,我们确定斑马鱼IRF6是IFN转录的正调节因子,并且可被MyD88和TBK1磷酸化。首先,用聚肌胞苷酸(一种病毒RNA模拟物)处理可上调细胞irf6的转录水平,这表明IRF6可能参与宿主细胞对病毒的反应过程。IRF6的过表达可显著上调IFN启动子活性,这意味着IRF6是IFN转录的正调节因子。随后,在蛋白质调节水平和相互作用关系方面,IRF6被MyD88和TBK1磷酸化并与其相关联。此外,IRF6的过表达激活了宿主细胞中isg15、rig-i和mavs的转录;同时,在IRF6过表达的细胞中,鲤春病毒血症病毒的p、m和n基因的转录物显著下降。综上所述,我们的数据表明,鱼类IRF6作为IFN转录的正调节因子并被MyD88和TBK1磷酸化,这与哺乳动物的同源物不同,表明低等和高等脊椎动物之间存在IRF6调节模式的差异。