Guan H, Song C, Simon A E
Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst 01003, USA.
RNA. 1997 Dec;3(12):1401-12.
Satellite (sat-) RNA C, one of the nonessential subviral RNAs of turnip crinkle virus (TCV), is dependent on the TCV-encoded RNA-dependent RNA polymerase (RdRp) for its replication. Earlier work showed that a stem-loop structure at the 3' end of (+)-strand sat-RNA C is required for synthesis of (-)-strands in vitro using a partially purified, template-specific TCV RdRp (Song C, Simon AE, 1995, J Mol Biol 254:6-14). Cis-sequences on (-)-strands of sat-RNA C that can serve as separate promoters in vitro have now been defined. Two promoter sequences are located on (-)-strand sat-RNA C, one comprising 11 bases located near the 3' end, and the other consisting of 14 bases located 41 bases from the 5' end. Both promoter sequences contain multiple consecutive C residues followed by multiple consecutive purines and have no obvious secondary structure, suggesting that, along with hairpin structures, specific primary sequences can be recognized by the TCV RdRp. The 3'-proximal promoter sequence directed synthesis from the 3' terminus using (-)-strand templates with the natural sat-RNA 3' end (AUCCC-3'). When plasmid-derived bases were present at the 3' ends of the templates, both promoter sequences could direct the RdRp to initiate transcription internally at the multiple consecutive C residues within the promoters. This result suggests that multiple consecutive C residues are important for transcription initiation and that natural 3'-end sequences, when located at 3' termini, help the RdRp to initiate at the 3' end of the molecule.
卫星(sat-)RNA C是芜菁皱缩病毒(TCV)的非必需亚病毒RNA之一,其复制依赖于TCV编码的RNA依赖性RNA聚合酶(RdRp)。早期研究表明,在体外使用部分纯化的、模板特异性的TCV RdRp合成(-)链时,(+)链sat-RNA C 3'端的茎环结构是必需的(Song C,Simon AE,1995,《分子生物学杂志》254:6 - 14)。现已确定sat-RNA C(-)链上可作为体外独立启动子的顺式序列。两个启动子序列位于sat-RNA C(-)链上,一个由位于3'端附近的11个碱基组成,另一个由位于5'端41个碱基处的14个碱基组成。两个启动子序列都包含多个连续的C残基,后面跟着多个连续的嘌呤,且没有明显的二级结构,这表明,除了发夹结构外,特定的一级序列也能被TCV RdRp识别。3'近端启动子序列使用具有天然sat-RNA 3'端(AUCCC-3')的(-)链模板从3'末端指导合成。当模板的3'端存在质粒衍生的碱基时,两个启动子序列都能指导RdRp在启动子内的多个连续C残基处内部起始转录。这一结果表明多个连续的C残基对转录起始很重要,并且天然的3'端序列位于3'末端时,有助于RdRp在分子的3'端起始转录。