Davidson J F, Schiestl R H
Department of Cancer Cell Biology, Harvard School of Public Health, Boston, MA 02115, USA.
J Bacteriol. 2001 Aug;183(15):4580-7. doi: 10.1128/JB.183.15.4580-4587.2001.
Lethal heat stress generates oxidative stress in Saccharomyces cerevisiae, and anaerobic cells are several orders of magnitude more resistant than aerobic cells to a 50 degrees C heat shock. Here we characterize the oxidative effects of this heat stress. The thermoprotective effect in anaerobic cells was not due to expression of HSP104 or any other heat shock gene, raising the possibility that the toxicity of lethal heat shock is due mainly to oxidative stress. Aerobic but not anaerobic heat stress caused elevated frequencies of forward mutations and interchromosomal DNA recombination. Oxidative DNA repair glycosylase-deficient strains under aerobic conditions showed a powerful induction of forward mutation frequencies compared to wild-type cells, which was completely abolished under anaerobiosis. We also investigated potential causes for this oxygen-dependent heat shock-induced genetic instability. Levels of sulfhydryl groups, dominated mainly by the high levels of the antioxidant glutathione (reduced form) and levels of vitamin E, decreased after aerobic heat stress but not after anaerobic heat stress. Aerobic heat stress also led to an increase in mitochondrial membrane disruption of several hundredfold, which was 100-fold reduced under anaerobic conditions.
致死性热应激在酿酒酵母中产生氧化应激,并且厌氧细胞对50摄氏度热激的抗性比需氧细胞高几个数量级。在此我们描述这种热应激的氧化效应。厌氧细胞中的热保护作用并非由于HSP104或任何其他热休克基因的表达,这增加了致死性热激毒性主要归因于氧化应激的可能性。需氧而非厌氧热应激导致正向突变和染色体间DNA重组的频率升高。与野生型细胞相比,需氧条件下氧化DNA修复糖基化酶缺陷型菌株显示出正向突变频率的强烈诱导,而在厌氧条件下这种诱导完全消除。我们还研究了这种氧依赖性热激诱导的遗传不稳定性的潜在原因。巯基水平主要由高水平的抗氧化剂谷胱甘肽(还原形式)和维生素E水平主导,需氧热应激后降低,但厌氧热应激后未降低。需氧热应激还导致线粒体膜破坏增加数百倍,在厌氧条件下这种破坏减少100倍。