生物
核糖核酸
可药性
基因组
结构母题
RNA病毒
遗传学
结构蛋白
病毒学
计算生物学
西尼罗河病毒
病毒
进化生物学
病毒结构蛋白
抄写(语言学)
RNA聚合酶
核酸结构
病毒进化
RNA沉默
病毒蛋白
呼肠孤病毒科
最近的共同祖先
核酸二级结构
结构变异
病毒复制
RNA编辑
相互依存
病毒进入
作者
Lucille H. Tsao,Doug E. Brackney,Anna Marie Pyle
摘要
The RNA genome of West Nile Virus (WNV) folds into an elaborate series of RNA structural elements that are crucial for viral function. Among these elements, four pseudoknots (PKs) at the viral 3'-terminus, designated as SLII, SLIV, DBI, and DBII, are among the most crucial players in the overall flaviviral lifecycle. While many studies have focused on exploring the behavior of individual PKs, we investigated the collective role of all four PKs in viral growth and small flaviviral RNA (sfRNA) formation. Through mutational analyses and infectious models, we establish that the four PKs are interdependent and work synergistically to aid in the folding and compaction of the WNV 3'-terminal region. A striking hierarchy is observed in PK contributions to global folding and sfRNA formation, whereby SLIV plays the largest role, followed by DBI, DBII, and SLII. We also discover highly conserved RNA tertiary motifs within the PK assembly that are shared across flaviviruses, suggesting a new type of druggable target that may be of value in the search for pan-flaviviral therapeutics.
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