Key Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture and Rural Affairs, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 510300, Guangzhou, Guangdong Province, PR China; Guangdong Provincial Engineer Technology Research Center of Marine Biological Seed Industry, Guangzhou, Guangdong Province, PR China.
Key Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture and Rural Affairs, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 510300, Guangzhou, Guangdong Province, PR China; Guangdong Provincial Engineer Technology Research Center of Marine Biological Seed Industry, Guangzhou, Guangdong Province, PR China.
Fish Shellfish Immunol. 2019 Nov;94:1-9. doi: 10.1016/j.fsi.2019.08.060. Epub 2019 Aug 26.
Interferon regulatory factor 8 (IRF8) increases type I IFN transcription levels by binding to IFN promoters, thereby playing a role in innate immunity. Nevertheless, the detailed mechanism through which IRF8 regulates type II IFN in fish remains ambiguous. In the present study, two genes from the golden pompano (Trachinotus ovatus), IRF8 (ToIRF8) and IFN gamma (ToIFNγ), were identified in the IFN/IRF-based signalling pathway. The full-length ToIRF8 cDNA was composed of 2,141 bp and encoded a 421 amino acid polypeptide; the genomic DNA was 2,917 bp in length and consisted of 8 exons and 7 introns. The putative protein showed the highest sequence identity (90-92%) with fish IRF8 and possessed a DNA-binding domain (DBD), an IRF-association domain (IAD) and a nuclear localization signal (NLS) motif consistent with those of IRF8 in other vertebrates. Furthermore, the ToIRF8 transcripts were expressed in all examined tissues of healthy fish, with higher levels observed in the central nervous and immune relevant tissues. They were upregulated by polyinosinic acid: polycytidylic acid [poly (I: C)], lipopolysaccharide (LPS) and flagellin treatments in the blood, liver, intestine and kidney. The results from assays of subcellular localization showed that ToIRF8 was localized to the cytoplasm. Moreover, to investigate whether ToIRF8 was a regulator of ToIFNγ, a promoter analysis was performed using progressive deletion mutations of ToIFNγ. The results indicated that the region from -601 bp to -468 bp includes the core promoter. Mutation analyses indicated that the activity of the ToIFNγ promoter significantly decreased after the targeted mutation of the M1-M3 binding sites. Additionally, overexpressed ToIRF8 in vitro notably increased the expression of several IFN/IRF-based signalling pathway genes. These results suggest that IRF8 is vital in the defence of T. ovatus against bacterial infection and contributes to a better understanding of the transcriptional mechanisms of ToIRF8 on type II IFN in fish.
干扰素调节因子 8(IRF8)通过与 IFN 启动子结合增加 I 型 IFN 转录水平,从而在先天免疫中发挥作用。然而,IRF8 调节鱼类 II 型 IFN 的详细机制仍不清楚。在本研究中,从金鲳鱼(Trachinotus ovatus)中鉴定了干扰素/IRF 信号通路中的两个基因,IRF8(ToIRF8)和 IFNγ(ToIFNγ)。ToIRF8 的全长 cDNA 由 2141bp 组成,编码 421 个氨基酸多肽;基因组 DNA 长 2917bp,由 8 个外显子和 7 个内含子组成。假定蛋白与其他脊椎动物的鱼类 IRF8 具有最高的序列同一性(90-92%),并具有 DNA 结合结构域(DBD)、IRF 结合结构域(IAD)和核定位信号(NLS)基序。此外,ToIRF8 转录本在健康鱼类的所有检测组织中均有表达,在中枢神经系统和免疫相关组织中表达水平较高。在血液、肝脏、肠道和肾脏中,poly(I:C)、脂多糖(LPS)和鞭毛蛋白处理后,它们的表达水平上调。亚细胞定位试验的结果表明,ToIRF8 定位于细胞质。此外,为了研究 ToIRF8 是否是 ToIFNγ 的调节剂,对 ToIFNγ 的启动子进行了逐步缺失突变分析。结果表明,-601bp 至-468bp 区域包含核心启动子。突变分析表明,靶向突变 M1-M3 结合位点后,ToIFNγ 启动子的活性显著降低。此外,体外过表达 ToIRF8 显著增加了几种 IFN/IRF 信号通路基因的表达。这些结果表明,IRF8 在金鲳鱼抵抗细菌感染的防御中至关重要,并有助于更好地理解 ToIRF8 在鱼类 II 型 IFN 转录中的调控机制。