Department of Microbiology, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo, Japan.
Genes Cells. 2010 Feb;15(2):151-9. doi: 10.1111/j.1365-2443.2009.01372.x. Epub 2010 Jan 17.
We previously reported that transcription elongation factor S-II and RNA polymerase II subunit Rpb9 maintain transcriptional fidelity and contribute to oxidative stress resistance in yeast. Here we examined whether other transcription elongation-related factors affect transcriptional fidelity in vivo. Among the 17 mutants of transcription elongation-related factors analyzed, most were not responsible for maintaining transcriptional fidelity. This finding indicates that transcriptional fidelity is controlled by a limited number of transcription elongation-related factors including S-II and Rpb9 and not by all transcription elongation-related factors. In contrast, by screening rpb9Delta cell revertants for sensitivity to the oxidant menadione, we identified a novel mutation in RNA polymerase II, rpb1-G730D, which suppressed both reduced transcriptional fidelity and oxidative stress sensitivity. These findings suggest that the maintenance of transcriptional fidelity that is mediated by transcription machinery directly confers oxidative stress resistance.
我们之前报道过转录延伸因子 S-II 和 RNA 聚合酶 II 亚基 Rpb9 可以维持转录保真度并有助于酵母的抗氧化应激。在这里,我们研究了其他与转录延伸相关的因子是否会影响体内的转录保真度。在分析的 17 种转录延伸相关因子突变体中,大多数因子与维持转录保真度无关。这一发现表明,转录保真度由少数与转录延伸相关的因子控制,包括 S-II 和 Rpb9,而不是所有与转录延伸相关的因子。相比之下,通过筛选 rpb9Delta 细胞回复突变体对氧化剂 menadione 的敏感性,我们在 RNA 聚合酶 II 中发现了一个新的突变 rpb1-G730D,它抑制了转录保真度降低和氧化应激敏感性增加。这些发现表明,由转录机制介导的转录保真度的维持直接赋予了氧化应激抗性。