Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
J Mol Biol. 2024 Nov 15;436(22):168767. doi: 10.1016/j.jmb.2024.168767. Epub 2024 Aug 28.
Flaviviruses, such as West Nile and Dengue Virus, pose a significant and growing threat to global health. Central to the flavivirus life cycle are highly structured 5'- and 3'-untranslated regions (UTRs), which harbor conserved cis-acting RNA elements critical for viral replication and host adaptation. Despite their essential roles, detailed molecular insights into these RNA elements have been limited. By employing nuclear magnetic resonance (NMR) spectroscopy in conjunction with SAXS experiments, we determined the three-dimensional structure of the West Nile Virus (WNV) 3'-terminal stem-loop core, a highly conserved element critical for viral genome cyclization and replication. Single nucleotide mutations at several sites within this RNA abolish the ability of the virus to replicate. These critical sites are located within a short 18-nucleotide hairpin stem, a substructure notable for its conformational flexibility, while the adjoining main stem-loop adopts a well-defined extended helix interrupted by three non-Watson-Crick pairs. This study enhances our understanding of several metastable RNA structures that play key roles in regulating the flavivirus lifecycle, and thereby also opens up potential new avenues for the development of antivirals targeting these conserved RNA structures. In particular, the structure we observe suggests that the plastic junction between the small hairpin and the tail of the longer stem-loop could provide a binding pocket for small molecules, for example potentially stabilizing the RNA in a conformation which hinders the conformational rearrangements critical for viral replication.
黄病毒,如西尼罗河病毒和登革热病毒,对全球健康构成了重大且日益严重的威胁。黄病毒生命周期的核心是高度结构化的 5'- 和 3'-非翻译区 (UTR),其中包含对病毒复制和宿主适应至关重要的保守顺式作用 RNA 元件。尽管这些 RNA 元件具有重要作用,但对它们的详细分子见解仍然有限。通过结合使用核磁共振 (NMR) 光谱和 SAXS 实验,我们确定了西尼罗河病毒 (WNV) 3'-末端茎环核心的三维结构,这是一个高度保守的元件,对病毒基因组环化和复制至关重要。该 RNA 中的几个位点的单核苷酸突变会使病毒失去复制能力。这些关键位点位于一个短的 18 个核苷酸发夹茎内,该亚结构以其构象灵活性为特征,而相邻的主茎环则采用了定义明确的延伸螺旋,其中打断了三个非 Watson-Crick 对。这项研究增强了我们对几种在调节黄病毒生命周期中起关键作用的亚稳定 RNA 结构的理解,从而为针对这些保守 RNA 结构开发抗病毒药物开辟了新的途径。特别是,我们观察到的结构表明,小发夹和较长茎环尾部之间的塑性连接点可能为小分子提供结合口袋,例如可能稳定 RNA 使其处于阻碍病毒复制的关键构象重排的构象。