University of Tromsø, Faculty of Biosciences, Fisheries and Economics, Norwegian College of Fishery Science, Breivika, N-9037 Tromsø, Norway.
Mol Immunol. 2010 Jul;47(11-12):2005-14. doi: 10.1016/j.molimm.2010.04.015. Epub 2010 May 21.
Transcription factors of the interferon regulatory factor (IRF) family are major regulators of the early immune responses against viral infections. In particular, IRF1, IRF2, IRF3 and IRF7 of mammals are known to regulate the expression of type I interferons (IFNs), which constitute the obligate cytokines for antiviral defense. We therefore cloned the coding sequence of Atlantic salmon (As) IRF1, IRF2, IRF3 and IRF7B. Expression profiles were studied in Atlantic salmon TO cells after poly I:C (dsRNA) transfection, treatment with recombinant salmon IFNa1 and infection with infectious salmon anemia virus (ISAV). The main findings were that AsIRF1 was earliest up-regulated by all stimuli, while AsIRF3 and AsIRF7 had a similar activation profile induced at a slightly later time point. The ability to induce the Atlantic salmon IFNa1 promoter was measured in a luciferase reporter assay. The results showed that AsIRF1, AsIRF3 and AsIRF7B were able to induce the promoter in a dose-dependent manner. AsIRF2 repressed the promoter, while AsIRF7A and a splicing variant (AsIRF3D) lacking the interaction domain had almost no effect. Combination of AsIRF1 and AsIRF3 had a synergistic stimulatory effect on the promoter compared to each of the two IRFs alone. Overall, our findings suggest that AsIRF3 is the main regulator of salmon IFNa1 production along with AsIRF1, which is less potent. This confirms a similar role for salmon IRF3 as mammalian IRF3 to be one of the main IRFs eliciting salmon IFNa1 production. Surprisingly, AsIRF7A and AsIRF7B seemed to have a lesser role in salmon IFNa1 induction, which may indicate that these factors have a larger role in activating other IFN genes or interferon stimulatory genes of Atlantic salmon.
干扰素调节因子(IRF)家族的转录因子是抗病毒感染早期免疫反应的主要调节剂。特别是哺乳动物的 IRF1、IRF2、IRF3 和 IRF7 被认为调节 I 型干扰素(IFN)的表达,IFN 是抗病毒防御的必需细胞因子。因此,我们克隆了大西洋鲑(As)IRF1、IRF2、IRF3 和 IRF7B 的编码序列。研究了多聚 I:C(dsRNA)转染、重组鲑鱼 IFNα1 处理和传染性鲑鱼贫血病毒(ISAV)感染后 Atlantic salmon TO 细胞的表达谱。主要发现是,所有刺激物均最早上调 AsIRF1,而 AsIRF3 和 AsIRF7 则在稍晚的时间点具有相似的激活谱。在荧光素酶报告基因测定中测量了诱导大西洋鲑鱼 IFNα1 启动子的能力。结果表明,AsIRF1、AsIRF3 和 AsIRF7B 能够以剂量依赖的方式诱导启动子。AsIRF2 抑制启动子,而缺乏相互作用域的剪接变体(AsIRF3D)几乎没有影响。与两个 IRF 单独作用相比,AsIRF1 和 AsIRF3 的组合对启动子具有协同刺激作用。总体而言,我们的研究结果表明,AsIRF3 与 AsIRF1 一起是鲑鱼 IFNα1 产生的主要调节剂,而 AsIRF1 作用较弱。这证实了鲑鱼 IRF3 与哺乳动物 IRF3 相似的作用,即作为主要的 IRF 之一,可诱导鲑鱼 IFNα1 的产生。令人惊讶的是,AsIRF7A 和 AsIRF7B 在诱导鲑鱼 IFNα1 方面的作用似乎较小,这可能表明这些因子在激活大西洋鲑鱼其他 IFN 基因或干扰素刺激基因方面具有更大的作用。