Khalizev A E, Petrova O N, Shapiro N I
Genetika. 1975;10(7):43-54.
Spontaneous mutagenesis and mutagenesis induced by chemical mutagens in culture Chinese hamster cells were investigated. Appearance of mutations controlling the resistance to 6-mercaptopurine (6M) and reverse mutations to sensitivity was studied. The rate of spontaneous mutations of 6M resistance in cells studied was found to be sufficiently stable: it was independent on the repeated freezing of these cells and the duration of their cultivation. 5-bromodeoxyuridine (BUdR) has been shown to induce mutations to 6M resistance in cells of the 237i clone; the rate of induced mutations in some experiments as compared to the rate of spontaneous mutations was 1-2 orders higher. No clear-cut delay of phenotypic expression of BUdR-induced mutations was found. Seven independently arisen mutant clones were isolated. Five of them appeared spontaneously and two clones were induced by BUdR. Three spontaneously arisen clones were found to be reversible to sensitivity. The rate of reverse mutations in cells of the other four clones, did not exceed (2,3-3,5)-10(-6) per cell per generation. The rate of spontaneous reverse mutations in these clones was less at least one order lower as compared to the rate of spontaneous mutations to 6M-resistance. The attempts to induce reverse mutations to sensitivity by N-nitrosomethylurea in spontaneously reversible resistant cells and by BUdR in mutant cells arisen as a result of the treatment with the same agent proved unsuccessful. A method of estimation of experiment's resolving power is described for cases, when no expected events (in our study reverse mutations) were observed.
研究了中国仓鼠培养细胞中的自发诱变以及化学诱变剂诱导的诱变。研究了控制对6-巯基嘌呤(6M)抗性的突变的出现以及向敏感性的回复突变。发现所研究细胞中6M抗性的自发突变率足够稳定:它与这些细胞的反复冻存及其培养持续时间无关。已证明5-溴脱氧尿苷(BUdR)可诱导237i克隆细胞产生对6M的抗性突变;在某些实验中,诱导突变率与自发突变率相比高1-2个数量级。未发现BUdR诱导的突变的表型表达有明显延迟。分离出七个独立产生的突变克隆。其中五个是自发出现的,两个克隆是由BUdR诱导的。发现三个自发产生的克隆可回复为敏感型。其他四个克隆的细胞中的回复突变率不超过每细胞每代(2.3-3.5)×10^(-6)。与向6M抗性的自发突变率相比,这些克隆中的自发回复突变率至少低一个数量级。在用N-亚硝基甲基脲处理自发可逆的抗性细胞以及用相同试剂处理后产生的突变细胞中,试图诱导向敏感性的回复突变均未成功。描述了一种在未观察到预期事件(在我们的研究中为回复突变)的情况下估计实验分辨能力的方法。