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RNA 剪接连接酶 RTCB 通过与 RNA 解旋酶 DDX1 相互作用抑制固有免疫来促进甲型流感病毒复制。

The RNA-Splicing Ligase RTCB Promotes Influenza A Virus Replication by Suppressing Innate Immunity via Interaction with RNA Helicase DDX1.

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.

College of Animal Medicine, Huazhong Agricultural University, Wuhan, China.

出版信息

J Immunol. 2023 Sep 15;211(6):1020-1031. doi: 10.4049/jimmunol.2200799.

Abstract

The RNA-splicing ligase RNA 2',3'-cyclic phosphate and 5'-OH ligase (RTCB) is a catalytic subunit of the tRNA-splicing ligase complex, which plays an essential role in catalyzing tRNA splicing and modulating the unfolded protein response. However, the function of RTCB in influenza A virus (IAV) replication has not yet been described. In this study, RTCB was revealed to be an IAV-suppressed host factor that was significantly downregulated during influenza virus infection in several transformed cell lines, as well as in primary human type II alveolar epithelial cells, and its knockout impaired the propagation of the IAV. Mechanistically, RTCB depletion led to a robust elevation in the levels of type I and type III IFNs and proinflammatory cytokines in response to IAV infection, which was confirmed by RTCB overexpression studies. Lastly, RTCB was found to compete with DDX21 for RNA helicase DDX1 binding, attenuating the DDX21-DDX1 association and thus suppressing the expression of IFN and downstream IFN-stimulated genes. Our study indicates that RTCB plays a critical role in facilitating IAV replication and reveals that the RTCB-DDX1 binding interaction is an important innate immunomodulator for the host to counteract viral infection.

摘要

RNA 2',3'-环磷酸和 5'-OH 连接酶(RTCB)是 tRNA 剪接连接酶复合物的催化亚基,在催化 tRNA 剪接和调节未折叠蛋白反应中发挥重要作用。然而,RTCB 在甲型流感病毒(IAV)复制中的功能尚未描述。在这项研究中,RTCB 被揭示为一种 IAV 抑制的宿主因子,在几种转化细胞系以及原代人 II 型肺泡上皮细胞中流感病毒感染时显著下调,其敲除会损害 IAV 的传播。在机制上,RTCB 耗竭导致 IAV 感染后 I 型和 III 型 IFN 和促炎细胞因子的水平大幅升高,这通过 RTCB 过表达研究得到证实。最后,发现 RTCB 与 DDX21 竞争 RNA 解旋酶 DDX1 的结合,从而减弱 DDX21-DDX1 复合物的形成,抑制 IFN 和下游 IFN 刺激基因的表达。我们的研究表明,RTCB 在促进 IAV 复制中发挥关键作用,并揭示了 RTCB-DDX1 结合相互作用是宿主抵抗病毒感染的重要先天免疫调节剂。

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