Department of Chemistry, University of Washington, Seattle, WA, USA, 98195.
Department of Chemistry, University of Washington, Seattle, WA, USA, 98195.
Biochem Biophys Res Commun. 2020 Oct 22;531(4):522-527. doi: 10.1016/j.bbrc.2020.07.115. Epub 2020 Aug 15.
Flaviviruses are major emerging human pathogenic viruses that pose a persistent and growing menace to global health. They are enveloped single-stranded RNA viruses with positive polarity transmitted by arthropod vectors like mosquitoes or ticks, responsible for a significant and growing number of human deaths and illnesses. The 5'- and 3'-untranslated regions (UTRs) are highly structured and contain conserved cis-acting RNA elements that participate in viral translation, replication and host adaptation. Despite their role in fiaviviruses replication, few high-resolution structural studies have investigated the RNA elements required for viral replication. Here we report the NMR structures of stem-loop B from WNV and DENV4 viruses. Because this element is required for cyclization of the genome and the activity of the replicative viral enzymes, viral replication rates are sensitive to even small changes in these RNAs. Therefore, this work provides structural insight into a new drug target to reduce flavivirus replication rates.
黄病毒是主要的新兴人类致病病毒,对全球健康构成持续且日益严重的威胁。它们是带包膜的单链 RNA 病毒,具有正链极性,通过蚊子或蜱等节肢动物传播,导致大量人类死亡和疾病。5' 和 3'非翻译区(UTR)高度结构化,包含参与病毒翻译、复制和宿主适应的保守顺式作用 RNA 元件。尽管它们在黄病毒复制中起作用,但很少有高分辨率结构研究调查复制所需的 RNA 元件。在这里,我们报告了来自 WNV 和 DENV4 病毒的茎环 B 的 NMR 结构。由于该元件是基因组环化和复制酶活性所必需的,因此病毒复制率对这些 RNA 的微小变化非常敏感。因此,这项工作为降低黄病毒复制率的新药物靶点提供了结构见解。