Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.
Section of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Microbial Pathogenesis, Yale School of Medicine, New Haven, CT 06520, USA.
Mol Cell. 2022 May 5;82(9):1631-1642.e6. doi: 10.1016/j.molcel.2022.02.031. Epub 2022 Mar 21.
Innate immune responses induce hundreds of interferon-stimulated genes (ISGs). Viperin, a member of the radical S-adenosyl methionine (SAM) superfamily of enzymes, is the product of one such ISG that restricts the replication of a broad spectrum of viruses. Here, we report a previously unknown antiviral mechanism in which viperin activates a ribosome collision-dependent pathway that inhibits both cellular and viral RNA translation. We found that the radical SAM activity of viperin is required for translation inhibition and that this is mediated by viperin's enzymatic product, 3'-deoxy-3',4'-didehydro-CTP (ddhCTP). Viperin triggers ribosome collisions and activates the MAPKKK ZAK pathway that in turn activates the GCN2 arm of the integrated stress response pathway to inhibit translation. The study illustrates the importance of translational repression in the antiviral response and identifies viperin as a translation regulator in innate immunity.
先天免疫反应诱导数百种干扰素刺激基因(ISGs)。Viperin 是活性 S-腺苷甲硫氨酸(SAM)超家族酶的成员之一,是限制广谱病毒复制的一种 ISG 的产物。在这里,我们报告了一个以前未知的抗病毒机制,其中 Viperin 激活了一种依赖于核糖体碰撞的途径,该途径抑制细胞和病毒 RNA 的翻译。我们发现 Viperin 的激进 SAM 活性是翻译抑制所必需的,并且这是由 Viperin 的酶产物 3'-脱氧-3',4'-二氢-CTP(ddhCTP)介导的。Viperin 引发核糖体碰撞并激活 MAPKKK ZAK 途径,该途径反过来激活整合应激反应途径的 GCN2 臂以抑制翻译。该研究说明了翻译抑制在抗病毒反应中的重要性,并确定 Viperin 是先天免疫中的翻译调节剂。