Department of Cell Biology and Molecular Genetics, University of Maryland College Park, College Park, Maryland, USA.
J Virol. 2012 Apr;86(8):4065-81. doi: 10.1128/JVI.07019-11. Epub 2012 Feb 15.
The majority of the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) was previously identified as forming a highly interactive structure with a ribosome-binding tRNA-shaped structure (TSS) acting as a scaffold and undergoing a widespread conformational shift upon binding to RNA-dependent RNA polymerase (RdRp). Tertiary interactions in the region were explored by identifying two highly detrimental mutations within and adjacent to a hairpin H4 upstream of the TSS that reduce translation in vivo and cause identical structural changes in the loop of the 3' terminal hairpin Pr. Second-site changes that compensate for defects in translation/accumulation and reverse the structural differences in the Pr loop were found in the Pr stem, as well as in a specific stem within the TSS and within the capsid protein (CP) coding region, suggesting that the second-site changes were correcting a conformational defect and not restoring specific base pairing. The RdRp-mediated conformational shift extended upstream through this CP open reading frame (ORF) region after bypassing much of an intervening, largely unstructured region, supporting a connection between 3' elements and coding region elements. These data suggest that the Pr loop, TSS, and H4 are central elements in the regulation of translation and replication in TCV and allow for development of an RNA interactome that maps the higher-order structure of a postulated RNA domain within the 3' region of a plus-strand RNA virus.
芜菁黄花叶病毒(TCV)的 3' 非翻译区(UTR)的大部分区域之前被确定为与核糖体结合的 tRNA 形结构(TSS)形成高度相互作用的结构,该结构作为支架,在与 RNA 依赖性 RNA 聚合酶(RdRp)结合时会发生广泛的构象变化。通过鉴定 TSS 上游发夹 H4 内及其附近的两个高度有害突变,探索了该区域的三级相互作用,这两个突变降低了体内翻译并导致 3'末端发夹 Pr 环的相同结构变化。在 Pr 茎以及 TSS 内的特定茎和衣壳蛋白(CP)编码区中发现了补偿翻译/积累缺陷并逆转 Pr 环结构差异的第二部位变化,表明第二部位变化正在纠正构象缺陷,而不是恢复特定的碱基配对。RdRp 介导的构象变化在绕过大部分 intervening 的、主要无结构区域后,通过该 CP 开放阅读框(ORF)区域向上游延伸,支持 3' 元件和编码区元件之间的连接。这些数据表明,Pr 环、TSS 和 H4 是 TCV 翻译和复制调控的核心元件,并允许开发 RNA 相互作用组,该组映射假定的 RNA 结构域在正链 RNA 病毒 3' 区的高级结构。