Saiga H, Higashinakagawa T
Nucleic Acids Res. 1979;6(5):1929-40. doi: 10.1093/nar/6.5.1929.
Some properties of in vitro transcription by isolated Xenopus oocyte nucleoli were described. When incubated with labeled RNA precursors, Xenopus oocyte nucleoli exhibited prolonged incorporation of radioactivity into RNA. The synthetic activity was exclusively due to type I RNA polymerase as revealed by its insensitivity to low and high doses of alpha-amanitin. The size of the in vitro transcript was mostly larger than 28S at 10 minute incubation and became smaller as incubation proceeded. When [gamma-32P]ATP was included in the reaction mixture, 32P radioactivity was incorporated into RNA suggesting the possible initiation of transcription in this system. However, analysis of the terminal nucleotide of the transcript revealed that the incorporation of radioactivity from [gamma-32P]ATP was not due to the initiation of transcription but due to polynucleotide kinase activity in the nucleolar preparation. These results demonstrate that the incorporation of radioactivity from [gamma-32P] labeled nucleoside triphosphates cannot necessarily be regarded as an index of the initiation of transcription.
本文描述了爪蟾卵母细胞核仁体外转录的一些特性。当与标记的RNA前体一起孵育时,爪蟾卵母细胞核仁表现出将放射性持续掺入RNA的现象。如对低剂量和高剂量α-鹅膏蕈碱不敏感所显示,合成活性完全归因于I型RNA聚合酶。体外转录本在孵育10分钟时大多大于28S,且随着孵育进行而变小。当反应混合物中包含[γ-32P]ATP时,32P放射性被掺入RNA,提示该系统可能存在转录起始。然而,对转录本末端核苷酸的分析表明,[γ-32P]ATP的放射性掺入并非由于转录起始,而是由于核仁制剂中的多核苷酸激酶活性。这些结果表明,[γ-32P]标记的核苷三磷酸的放射性掺入不一定能被视为转录起始的指标。