Department of Molecular Biology, Princeton University, Princeton, NJ, USA.
PLoS Genet. 2013;9(8):e1003680. doi: 10.1371/journal.pgen.1003680. Epub 2013 Aug 1.
Conditions of chronic stress are associated with genetic instability in many organisms, but the roles of stress responses in mutagenesis have so far been elucidated only in bacteria. Here, we present data demonstrating that the environmental stress response (ESR) in yeast functions in mutagenesis induced by proteotoxic stress. We show that the drug canavanine causes proteotoxic stress, activates the ESR, and induces mutagenesis at several loci in an ESR-dependent manner. Canavanine-induced mutagenesis also involves translesion DNA polymerases Rev1 and Polζ and non-homologous end joining factor Ku. Furthermore, under conditions of chronic sub-lethal canavanine stress, deletions of Rev1, Polζ, and Ku-encoding genes exhibit genetic interactions with ESR mutants indicative of ESR regulating these mutagenic DNA repair processes. Analyses of mutagenesis induced by several different stresses showed that the ESR specifically modulates mutagenesis induced by proteotoxic stress. Together, these results document the first known example of an involvement of a eukaryotic stress response pathway in mutagenesis and have important implications for mechanisms of evolution, carcinogenesis, and emergence of drug-resistant pathogens and chemotherapy-resistant tumors.
慢性应激条件与许多生物体中的遗传不稳定性有关,但迄今为止,应激反应在诱变中的作用仅在细菌中得到阐明。在这里,我们提供的数据表明,酵母中的环境应激反应 (ESR) 在由蛋白毒性应激诱导的诱变中起作用。我们表明,药物-canavanine- 会导致蛋白毒性应激,激活 ESR,并以 ESR 依赖性方式在几个基因座诱导诱变。Canavanine 诱导的诱变还涉及跨损伤 DNA 聚合酶 Rev1 和 Polζ 和非同源末端连接因子 Ku。此外,在慢性亚致死 canavanine 应激条件下,Rev1、Polζ 和 Ku 编码基因的缺失与 ESR 突变体表现出遗传相互作用,表明 ESR 调节这些诱变 DNA 修复过程。对几种不同应激诱导的诱变分析表明,ESR 特异性调节由蛋白毒性应激诱导的诱变。总之,这些结果记录了真核应激反应途径参与诱变的第一个已知实例,对进化、致癌、耐药病原体和化疗耐药肿瘤的出现机制具有重要意义。