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IRF11 与 STAT1 和 STAT2 协同作用促进 I 型 IFN 的产生。

IRF11 synergizes with STAT1 and STAT2 to promote type I IFN production.

机构信息

Fisheries College, Jimei University, Xiamen, 361021, PR China.

Fisheries College, Jimei University, Xiamen, 361021, PR China; Engineering Research Center of the Modern Technology for Eel Industry, Ministry of Education, PR China.

出版信息

Fish Shellfish Immunol. 2024 Jul;150:109656. doi: 10.1016/j.fsi.2024.109656. Epub 2024 May 25.

Abstract

Interferon regulatory factor 11 (IRF11), a fish specific member of IRF family, is a transcription factor known for its positive role in teleost antiviral defense by regulating IFN expression. Despite its recognized function, the precise mechanism of IRF11 in type I IFNs production remains largely unknown. In this study, we identified IRF11 in Japanese eel, Anguilla japonica, (AjIRF11) and determined its involvement in the later phase of fish IFN production. Our results demonstrate that IRF11-induced IFN production operates through ISRE binding. Mutations in each ISRE site within the promoter of AjIFN2 or AjIFN4 abolished IRF11-mediated activation of IFN promoters. In addition, the overexpression of AjIRF11 does not significantly impact the activation of AjIFN promoters induced by RLR-related signaling pathway proteins. Furthermore, IRF11-knockdown in ZFLs (zebrafish liver cells) has no effect on the RLRs-induced expression of zebrafish IFN-φ1 and IFN-φ3, indicating that IRF11 is not involved in the RLR-mediated IFN production. However, AjIRF11 can form transcription complexes with AjSTAT1 or AjSTAT2, or form homo- or heterodimers with AjIRF1 to stimulate the transcription of type I IFNs. Overall, it is shown in this study that IRF11 can act synergistically with STAT1 and/or STAT2 for the induction of IFN.

摘要

干扰素调节因子 11(IRF11)是 IRF 家族中鱼类特有的成员,作为一种转录因子,通过调节 IFN 的表达,在硬骨鱼类抗病毒防御中发挥积极作用。尽管其功能已被广泛认可,但 IRF11 在 I 型 IFNs 产生中的确切机制仍知之甚少。在本研究中,我们在日本鳗鲡(Anguilla japonica)中鉴定出了 IRF11(AjIRF11),并确定了其在鱼类 IFN 产生的后期阶段中的作用。研究结果表明,IRF11 诱导 IFN 产生是通过 ISRE 结合来实现的。在 AjIFN2 或 AjIFN4 启动子内的每个 ISRE 位点发生突变,均会使 IRF11 介导的 IFN 启动子激活失效。此外,AjIRF11 的过表达对 RLR 相关信号通路蛋白诱导的 AjIFN 启动子的激活没有显著影响。此外,IRF11 在 ZFLs(斑马鱼肝细胞)中的敲低对 RLRs 诱导的斑马鱼 IFN-φ1 和 IFN-φ3 的表达没有影响,表明 IRF11 不参与 RLR 介导的 IFN 产生。然而,AjIRF11 可以与 AjSTAT1 或 AjSTAT2 形成转录复合物,或与 AjIRF1 形成同源或异源二聚体,以刺激 I 型 IFNs 的转录。总的来说,本研究表明,IRF11 可以与 STAT1 和/或 STAT2 协同作用诱导 IFN。

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