Nagley P, Mattick J S, Hall R M, Linnane A W
Mol Gen Genet. 1975 Dec 9;141(4):291-304. doi: 10.1007/BF00331451.
The action of ethidium bromide and berenil on the mitochondrial genome of Saccharomyces cerevisiae has been compared in three types of study: (i) early kinetics (up to 4 h) of petite induction by the drugs in the presence or absence of sodium dodecyl sulphate; (ii) genetic consequences of long-term (8 cell generations) exposure to the drugs; (iii) inhibition of mitochondrial DNA replication, both in whole cells and in isolated mitochondria. The results have been interpreted as follows. Firstly, the early events in petite induction differ markedly for the two drugs, as indicated by differences in the short-term kinetics. After some stage a common pathway is apparently followed because the composition of the population of petite cells induced after long-term exposure are very similar for both ethidium bromide and berenil. Secondly, both drugs probably act at the same site to inhibit mitochondrial DNA replication, in view of the fact that a petite strain known to be resistant to ethidium bromide inhibition of mitochondrial DNA replication was found to have simultaneously acquired resistance to berenil. From consideration of the drug concentrations needed to inhibit mitochondrial DNA replication in vivo and in vitro it is suggested that in vivo permeability barriers impede the access of ethidium bromide to the site of inhibition of mitochondrial DNA replication, whilst access of berenil to this site is facilitated. The site at which the drugs act to inhibit mitochondrial DNA replication may be different from the site(s) involved in early petite induction. Binding of the drugs at the latter site(s) is considered to initiate a series of events leading to the fragmentation of yeast mitochondrial DNA and petite induction.
(i)在有或没有十二烷基硫酸钠存在的情况下,药物诱导小菌落形成的早期动力学(长达4小时);(ii)长期(8个细胞世代)暴露于药物的遗传后果;(iii)在全细胞和分离的线粒体中对线粒体DNA复制的抑制。结果如下解释。首先,两种药物诱导小菌落形成的早期事件明显不同,如短期动力学的差异所示。在某个阶段之后,显然遵循共同途径,因为长期暴露后诱导的小菌落细胞群体的组成对于溴化乙锭和贝尼尔非常相似。其次,鉴于发现一种已知对溴化乙锭抑制线粒体DNA复制具有抗性的小菌落菌株同时获得了对贝尼尔的抗性,两种药物可能作用于同一部位以抑制线粒体DNA复制。从体内和体外抑制线粒体DNA复制所需的药物浓度考虑,表明体内通透性屏障阻碍溴化乙锭进入线粒体DNA复制抑制部位,而贝尼尔进入该部位则更容易。药物作用于抑制线粒体DNA复制的部位可能与早期小菌落诱导所涉及的部位不同。药物在后者部位的结合被认为引发一系列导致酵母线粒体DNA片段化和小菌落诱导的事件。