Pooggin Mikhail M, Fütterer Johannes, Skryabin Konstantin G, Hohn Thomas
Centre 'Bioengineering', Russian Academy of Sciences, 117312 Moscow, Russia2.
Friedrich Miescher Institute, PO Box 2543, CH-4002 Basel, Switzerland1.
J Gen Virol. 1999 Aug;80 ( Pt 8):2217-2228. doi: 10.1099/0022-1317-80-8-2217.
In plant pararetroviruses, pregenomic RNA (pgRNA) directs synthesis of circular double-stranded viral DNA and serves as a polycistronic mRNA. By computer-aided analysis, the 14 plant pararetroviruses sequenced so far were compared with respect to structural organization of their pgRNA 5'-leader. The results revealed that the pgRNA of all these viruses carries a long leader sequence containing several short ORFs and having the potential to form a large stem-loop structure; both features are known to be inhibitory for downstream translation. Formation of the structure brings the first long ORF into the close spatial vicinity of a 5'-proximal short ORF that terminates 5 to 10 nt upstream of the stable structural element. The first long ORF on the pgRNA is translated by a ribosome shunt mechanism discovered in cauliflower mosaic (CaMV) and rice tungro bacilliform viruses, representing the two major groups of plant pararetroviruses. Both the short ORF and the structure have been implicated in the shunt process for CaMV pgRNA translation. The conservation of these elements among all plant pararetroviruses suggests conservation of the ribosome shunt mechanism. For some of the less well-studied viruses, the localization of the conserved elements also allowed predictions of the pgRNA promoter region and the translation start site of the first long ORF.
在植物类逆转录病毒中,前基因组RNA(pgRNA)指导环状双链病毒DNA的合成,并作为多顺反子mRNA发挥作用。通过计算机辅助分析,对目前已测序的14种植物类逆转录病毒的pgRNA 5'端前导序列的结构组织进行了比较。结果显示,所有这些病毒的pgRNA都带有一个长的前导序列,其中包含几个短的开放阅读框(ORF),并且有可能形成一个大的茎环结构;这两个特征都已知对下游翻译具有抑制作用。该结构的形成使第一个长ORF与一个5'近端短ORF在空间上紧密相邻,该短ORF在稳定结构元件上游5至10个核苷酸处终止。pgRNA上的第一个长ORF通过在花椰菜花叶病毒(CaMV)和水稻东格鲁杆状病毒中发现的核糖体跳跃机制进行翻译,这两种病毒代表了植物类逆转录病毒的两个主要类别。短ORF和结构都与CaMV pgRNA翻译的跳跃过程有关。所有植物类逆转录病毒中这些元件的保守性表明核糖体跳跃机制是保守的。对于一些研究较少的病毒,保守元件的定位也有助于预测pgRNA启动子区域和第一个长ORF的翻译起始位点。