Chen Yixia, Li Jun, Fu Jiaxin, Xiao Lili, Chu Jixiang, Qin Wei, Xiao Jun, Feng Hao
State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Science, Hunan Normal University, Changsha, 410081, China.
Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, College of Biological and Food Engineering, Huaihua University, Huaihua, 418008, China.
Fish Shellfish Immunol. 2025 Feb;157:110097. doi: 10.1016/j.fsi.2024.110097. Epub 2024 Dec 24.
Mammalian SUMO specific peptidase 2 (SENP2) plays vital roles in a variety of biological procedures including the immune response. However, the effects of teleost SENP2 are still mostly unexplored. In this study, the SENP2 of black carp (Mylopharyngodon piceus) was cloned and characterized. The open reading frame of black carp SENP2 (bcSENP2) consists of 1800 nucleotides, which encode 600 amino acids. The reporter assay results showed that over-expression of bcSENP2 alone had a weak effect on interferon (IFN) promoter transcription activity, whereas it significantly reduced bcMDA5/bcRIG-I mediated IFN promoter transcription activity. The interaction between bcSENP2 and bcMDA5 or bcRIG-I was detected by immunoprecipitation experiments. The plaque assay and qPCR results indicated that bcMDA5 or bcRIG-I mediated antiviral capacity was attenuated by bcSENP2, while knockdown of bcSENP2 led to enhanced antiviral resistance to SVCV in host cells. In addition, the expression level of bcMDA5/bcRIG-I protein was attenuated by co-expressed bcSENP2 and MG132 treatment rescued this attenuating effect. All of these data support the conclusion that bcSENP2 inhibits bcMDA5/bcRIG-I mediated antiviral signaling by enhancing ubiquitin-proteasome mediated degradation of bcMDA5/bcRIG-I in black carp.
哺乳动物的SUMO特异性蛋白酶2(SENP2)在包括免疫反应在内的多种生物学过程中发挥着至关重要的作用。然而,硬骨鱼SENP2的作用仍大多未被探索。在本研究中,对草鱼(Mylopharyngodon piceus)的SENP2进行了克隆和表征。草鱼SENP2(bcSENP2)的开放阅读框由1800个核苷酸组成,编码600个氨基酸。报告基因检测结果表明,单独过表达bcSENP2对干扰素(IFN)启动子转录活性的影响较弱,而它显著降低了bcMDA5/bcRIG-I介导的IFN启动子转录活性。通过免疫沉淀实验检测了bcSENP2与bcMDA5或bcRIG-I之间的相互作用。噬斑测定和qPCR结果表明,bcSENP2减弱了bcMDA5或bcRIG-I介导的抗病毒能力,而敲低bcSENP2导致宿主细胞对鲤春病毒血症病毒(SVCV)的抗病毒抗性增强。此外,共表达bcSENP2会减弱bcMDA5/bcRIG-I蛋白的表达水平,而MG132处理可挽救这种减弱作用。所有这些数据支持以下结论:bcSENP2通过增强泛素-蛋白酶体介导的草鱼bcMDA5/bcRIG-I降解来抑制bcMDA5/bcRIG-I介导的抗病毒信号传导。