Oliver S G, Williamson D H
Mol Gen Genet. 1976 Aug 2;146(3):261-8. doi: 10.1007/BF00701249.
Cytoplasmic petite mutagenesis by 5-fluorouracil (5FU) was prevented by temperature sensitive mutations which blcoked either nuclear transcription or cytoplasmic translation. However, 5FU was also ineffective in resting cells and in cells exposed to alpha-mating factor, showing that cell division or nuclear DNA synthesis is required for the mutagenic event to take place. In addition, the mutagenic effect of 5FU was completely prevented by daunomycin, and since this agent preferentially inhibits respiratory growth and was shown to selectively block RNA synthesis in the mitochondria, it was concluded that petite mutagensis resulted from incorporation of 5FU into mitochondrial RNA. Since inhibition of mitochondrial protein synthesis by erythromycin had little immediate effect on the mutagenicity of 5FU, it was deduced that the RNA in question is not directly involved in mitochondrial translation, and may have a regulatory function.
5-氟尿嘧啶(5FU)诱导的细胞质小菌落突变可被温度敏感突变所阻止,这些温度敏感突变会阻断核转录或细胞质翻译。然而,5FU在静止细胞和暴露于α-交配因子的细胞中也无效,这表明诱变事件发生需要细胞分裂或核DNA合成。此外,柔红霉素可完全阻止5FU的诱变作用,由于该药物优先抑制呼吸生长,并已证明可选择性地阻断线粒体中的RNA合成,因此得出结论,小菌落突变是由于5FU掺入线粒体RNA所致。由于红霉素对线粒体蛋白质合成的抑制对5FU的诱变性几乎没有直接影响,因此推断所讨论的RNA不直接参与线粒体翻译,可能具有调节功能。