Cheng J H, Ding M P, Hsu Y H, Tsai C H
Graduate Institute of Agricultural Biotechnology, National Chung Hsing University, 402, Taichung, Taiwan, ROC.
Virus Res. 2001 Nov 28;80(1-2):41-52. doi: 10.1016/s0168-1702(01)00348-3.
RNA-dependent RNA polymerases (RdRp) isolated from bamboo mosaic potexvirus (BaMV) and potato virus X infected Nicotiana benthamiana plants and solubilized with the detergent NP-40, generated a full-length genomic and two subgenomic double-stranded RNAs of respective viruses in an in vitro RdRp assay containing endogenous RNA templates. Template-dependent and species-specific RdRp activity could be detected after the removal of endogenous RNA templates. The 3' untranslated regions (UTR) containing a stretch of 40 adenylate residues were shown to be an efficient exogenous RNA template for in vitro RdRp reactions. Solution hybridization and nuclease digestion studies revealed that the products transcribed in vitro were minus-sense. Besides using the 3' UTR for minus-sense RNA synthesis, the BaMV RdRp can also recognize 3' terminal 77 nucleotides of the minus-strand for plus-sense RNA synthesis. Promoter studies with BaMV RdRp showed that domain D containing the potexviral hexamer motif of the 3' UTR would be the major contributor of minus-sense RNA synthesis in vitro. On the other hand, the pseudoknot domain containing the poly(A) sequences would be sufficient for minus-sense RNA synthesis.
从感染了竹花叶病毒(BaMV)和马铃薯X病毒的本氏烟草植株中分离出RNA依赖性RNA聚合酶(RdRp),并用去污剂NP-40使其溶解,在含有内源性RNA模板的体外RdRp测定中,产生了相应病毒的全长基因组双链RNA和两个亚基因组双链RNA。去除内源性RNA模板后,可检测到模板依赖性和物种特异性的RdRp活性。含有一段40个腺苷酸残基的3'非翻译区(UTR)被证明是体外RdRp反应的有效外源性RNA模板。溶液杂交和核酸酶消化研究表明,体外转录的产物是负链。除了使用3'UTR进行负链RNA合成外,BaMV RdRp还可以识别负链的3'末端77个核苷酸用于正链RNA合成。对BaMV RdRp的启动子研究表明,含有3'UTR的马铃薯X病毒六聚体基序的结构域D将是体外负链RNA合成的主要贡献者。另一方面,含有聚(A)序列的假结结构域足以进行负链RNA合成。