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N6-甲基腺苷阅读蛋白 YTHDC1 调控甲型流感病毒 NS 节段的剪接和复制。

N6-methyladenosine reader protein YTHDC1 regulates influenza A virus NS segment splicing and replication.

机构信息

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

Key Laboratory of Preventive Veterinary Medicine in Hubei Province, Cooperative Innovation Center for Sustainable Pig Production, Wuhan, China.

出版信息

PLoS Pathog. 2023 Apr 13;19(4):e1011305. doi: 10.1371/journal.ppat.1011305. eCollection 2023 Apr.

Abstract

N6-methyladenosine (m6A) modification on viral RNAs has a profound impact on infectivity. m6A is also a highly pervasive modification for influenza viral RNAs. However, its role in virus mRNA splicing is largely unknown. Here, we identify the m6A reader protein YTHDC1 as a host factor that associates with influenza A virus NS1 protein and modulates viral mRNA splicing. YTHDC1 levels are enhanced by IAV infection. We demonstrate that YTHDC1 inhibits NS splicing by binding to an NS 3' splicing site and promotes IAV replication and pathogenicity in vitro and in vivo. Our results provide a mechanistic understanding of IAV-host interactions, a potential therapeutic target for blocking influenza virus infection, and a new avenue for the development of attenuated vaccines.

摘要

N6-甲基腺苷(m6A)修饰对病毒 RNA 的感染力有深远影响。m6A 也是流感病毒 RNA 上一种高度普遍的修饰。然而,其在病毒 mRNA 剪接中的作用在很大程度上仍是未知的。在这里,我们鉴定出 m6A 阅读蛋白 YTHDC1 是一种与甲型流感病毒 NS1 蛋白结合并调节病毒 mRNA 剪接的宿主因子。YTHDC1 水平在 IAV 感染后增强。我们证明,YTHDC1 通过与 NS 3' 剪接位点结合来抑制 NS 剪接,并促进 IAV 在体外和体内的复制和致病性。我们的研究结果提供了对 IAV-宿主相互作用的机制理解,为阻止流感病毒感染提供了一个潜在的治疗靶点,并为减毒疫苗的开发开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5975/10146569/63d1c0afa661/ppat.1011305.g001.jpg

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