Ray Debashish, Wu Baodong, White K Andrew
Department of Biology, York University, Toronto, Ontario, Canada M3J 1P3.
RNA. 2003 Oct;9(10):1232-45. doi: 10.1261/rna.5630203.
The 5' untranslated regions (UTRs) of (+)-strand RNA viruses play a variety of roles in the reproductive cycles of these infectious agents. Tomato bushy stunt virus (TBSV) belongs to this class of RNA virus and is the prototype member of the genus Tombusvirus. Previous studies have demonstrated that a T-shaped domain (TSD) forms in the 5' half of the TBSV 5' UTR and that it plays a central role in viral RNA replication. Here we have extended our structure-function analysis to the 3' half of the 5' UTR. Investigation of this region in the context of a model viral replicon (i.e., a TBSV-derived defective interfering [DI] RNA) revealed that this segment contains numerous functionally relevant structural features. In vitro solution structure probing along with comparative and computer-aided RNA secondary structure analyses predicted the presence of a simple stem loop (SL5) followed by a more complex downstream domain (DSD). Both structures were found to be essential for efficient DI RNA accumulation when tested in a plant protoplast system. For SL5, maintenance of the base of its stem was the principal feature required for robust in vivo accumulation. In the DSD, both helical and unpaired regions containing conserved sequences were necessary for efficient DI RNA accumulation. Additionally, optimal DI RNA accumulation required a TSD-DSD interaction mediated by a pseudoknot. Modifications that reduced accumulation did not appreciably affect DI RNA stability in vivo, indicating that the DSD and SL5 act to facilitate viral RNA replication.
正链RNA病毒的5'非翻译区(UTR)在这些感染性因子的复制周期中发挥着多种作用。番茄丛矮病毒(TBSV)属于此类RNA病毒,是番茄病毒属的原型成员。先前的研究表明,在TBSV 5'UTR的5'半段形成了一个T形结构域(TSD),并且它在病毒RNA复制中起着核心作用。在这里,我们将结构-功能分析扩展到了5'UTR的3'半段。在模型病毒复制子(即源自TBSV的缺陷干扰[DI]RNA)的背景下对该区域进行研究发现,该片段包含许多功能相关的结构特征。体外溶液结构探测以及比较和计算机辅助RNA二级结构分析预测存在一个简单的茎环(SL5),其后是一个更复杂的下游结构域(DSD)。当在植物原生质体系统中进行测试时,发现这两种结构对于有效的DI RNA积累都是必不可少的。对于SL5,其茎基部的维持是体内强大积累所需的主要特征。在DSD中,包含保守序列的螺旋区和非配对区对于有效的DI RNA积累都是必需的。此外,最佳的DI RNA积累需要由假结介导的TSD-DSD相互作用。降低积累的修饰在体内并未明显影响DI RNA的稳定性,这表明DSD和SL5起到促进病毒RNA复制的作用。