Lee S Y, Uyeda I, Shikata E
Department of Botany, Faculty of Agriculture, Hokkaido University, Sapporo, Japan.
Intervirology. 1987;27(4):189-95. doi: 10.1159/000149984.
The RNA polymerase associated with rice ragged stunt virus (RRSV) was characterized. Activity was optimum at 35-40 degrees in 0.1 MTris-HC1 (pH 8.5) and 6-8 mMMgCl2. S-Adenosyl-L-methionine stimulated the activity about 5- to 6-fold. It was also stimulated in the presence of chymotrypsin (200 micrograms/ml). The molecular weights of RNAs synthesized in vitro were calculated to be about half those of the respective genome segments. The synthesized RNAs hybridized to the genome RNAs, and the hybrids migrated identically to the genome RNAs in PAGE. These results indicate that RRSV particles transcribe full-length copies of the genome RNAs. The characteristics of the polymerase are discussed in relation to those of other members of the Reoviridae.
对与水稻锯齿叶矮缩病毒(RRSV)相关的RNA聚合酶进行了特性分析。在含有0.1 M Tris-HCl(pH 8.5)和6 - 8 mM MgCl₂的体系中,35 - 40℃时活性最佳。S-腺苷-L-甲硫氨酸可使该活性提高约5至6倍。在存在胰凝乳蛋白酶(200微克/毫升)的情况下也会被激活。体外合成的RNA分子量经计算约为各自基因组片段分子量的一半。合成的RNA与基因组RNA杂交,且杂交产物在聚丙烯酰胺凝胶电泳(PAGE)中的迁移情况与基因组RNA相同。这些结果表明RRSV颗粒转录基因组RNA的全长拷贝。结合呼肠孤病毒科其他成员的聚合酶特性对该聚合酶的特性进行了讨论。