Laboratory of Fish Molecular Immunology, College of Fisheries and Life Science, Shanghai Ocean Universitygrid.412514.7, Shanghai, China.
Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources (grid.412514.7Shanghai Ocean University), Ministry of Education, Shanghai, China.
J Virol. 2022 Jan 12;96(1):e0148421. doi: 10.1128/JVI.01484-21. Epub 2021 Oct 13.
Long noncoding RNAs (lncRNAs) function as microregulatory factors that influence gene expression after a variety of pathogenic infections, and they have been extensively studied in the past few years. Although less attention has been paid to lncRNAs in lower vertebrates than in mammals, current studies reveals that lncRNAs play a vital role in fish stimulated by pathogens. Here, we discovered a new lncRNA, termed MIR2187HG, which can function as a precursor of a small RNA, miR-2187-3p, with regulatory functions in the miiuy croaker (Miichthys miiuy). Upon Siniperca chuatsi rhabdovirus (SCRV) virus infection, the expression levels of MIR2187HG were remarkably enhanced. Elevated MIR2187HG expression can act as a pivotally negative regulator that participates in the innate immune response of teleost fish to inhibit the intracellular TANK-binding kinase 1 (TBK1)-mediated antiviral signaling pathways, which can effectively avoid excessive immunity. In addition, we found that SCRV could also utilize MIR2187HG to enhance its own numbers. Our results not only provide evidence regarding the involvement of the lncRNAs in response to viruses in fish but also broaden our understanding of the function of lncRNAs as precursor microRNAs (miRNAs) in teleost fish for the first time. SCRV infection upregulates MIR2187HG levels, which in turn suppresses SCRV-triggered type I interferon production, thus promoting viral replication in miiuy croaker. Notably, MIR2187HG regulates the release of miR-2187-3p, and TBK1 is a target of miR-2187-3p. MIR2187HG could acquire from miR-2187-3p the function of inhibiting TBK1 expression and subsequently modulate TBK1-mediated NF-κB and IRF3 signaling. The collective results suggest that the novel regulation mechanism of TBK1-mediated antiviral response during RNA viral infection was regulated by MIR2187HG. Therefore, a new regulation mechanism for lncRNAs to regulate antiviral immune responses in fish is proposed.
长非编码 RNA(lncRNA)作为微调节因子,在多种致病感染后影响基因表达,近年来受到广泛研究。尽管与哺乳动物相比,人们对低等脊椎动物中的 lncRNA 的关注较少,但目前的研究表明,lncRNA 在鱼类受到病原体刺激时发挥着重要作用。在这里,我们发现了一种新的 lncRNA,称为 MIR2187HG,它可以作为小 RNA miR-2187-3p 的前体发挥作用,并在米氏绒螯蟹(Miichthys miiuy)中具有调节功能。在虹彩病毒(SCRV)病毒感染后,MIR2187HG 的表达水平显著增强。升高的 MIR2187HG 表达可以作为一个关键的负调节因子,参与鱼类的固有免疫反应,抑制细胞内 TANK 结合激酶 1(TBK1)介导的抗病毒信号通路,从而有效避免过度免疫。此外,我们发现 SCRV 也可以利用 MIR2187HG 来增加自身数量。我们的研究结果不仅提供了 lncRNA 参与鱼类病毒反应的证据,而且首次拓宽了我们对 lncRNA 作为前体 microRNA(miRNA)在硬骨鱼类中的功能的理解。SCRV 感染上调 MIR2187HG 水平,进而抑制 SCRV 触发的 I 型干扰素产生,从而促进米氏绒螯蟹中的病毒复制。值得注意的是,MIR2187HG 调节 miR-2187-3p 的释放,而 TBK1 是 miR-2187-3p 的靶标。MIR2187HG 可以从 miR-2187-3p 获得抑制 TBK1 表达的功能,并随后调节 TBK1 介导的 NF-κB 和 IRF3 信号。这些结果表明,在 RNA 病毒感染过程中,MIR2187HG 调控了 TBK1 介导的抗病毒反应的新调控机制。因此,提出了一种新的调控机制,用于调控鱼类中的抗病毒免疫反应。