Structure of Essential RNA Regulatory Elements in the West Nile Virus 3′-Terminal Stem Loop

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-08-28 DOI:10.1016/j.jmb.2024.168767
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Abstract

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.

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西尼罗河病毒 3'- 末端茎环中重要 RNA 调控元件的结构。
西尼罗河病毒和登革热病毒等黄病毒对全球健康构成了日益严重的威胁。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 元件起着至关重要的作用,但对它们的详细分子研究却很有限。通过结合 SAXS 实验使用核磁共振(NMR)光谱,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素,对病毒基因组的环化和复制至关重要。该 RNA 中几个位点的单核苷酸突变会削弱病毒的复制能力。这些关键位点位于短短的 18 个核苷酸发夹茎中,这种子结构以其构象灵活性而著称,而相邻的主茎环则采用了明确的扩展螺旋,中间有三个非沃森-克里克对。这项研究加深了我们对在调控黄病毒生命周期中发挥关键作用的几种可转移 RNA 结构的了解,从而也为开发针对这些保守 RNA 结构的抗病毒药物开辟了潜在的新途径。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交界处可以为小分子提供一个结合口袋,例如有可能将 RNA 稳定在一个构象中,从而阻碍病毒复制过程中至关重要的构象重排。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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