Institut für Mikrobiologie, Johann Wolfgang Goethe-Universität, Theodor-Stern-Kai 7, Haus 75, 6000, Frankfurt, Germany.
Curr Genet. 1981 Nov;4(2):145-9. doi: 10.1007/BF00365693.
Selection of mutants of Saccharomyces cerevisiae sensitive to the DNA cross-linking agent nitrogen mustard (HN2) at two temperatures (23 °C and 36 °C) yielded two isolates with thermoconditionally enhanced (ts) sensitivity to the mutagen. Both were due to single recessive nuclear genes. Mutant allele snm1-2 (ts) showed mainly ts-sensitivity to HN2, whereas mutant allele snm2-1 (ts) conferred ts-sensitivity to HN2, half mustard (HN1) and UV. In temperature-shift experiments it was determined that the functions of SNM1 and SNM2 are needed for recovery within 6 to 7 h. after mutagen exposure during incubation at 23 °C on YEPD when HN2 and UV are applied. After HN1 treatment the SNM2 coded function is required for recovery for about 14 hrs. This possibly indicates a handling of UV- and HN2-induced lesions different from that of HN1-induced lesions.
在 23°C 和 36°C 两个温度下,选择对 DNA 交联剂氮芥(HN2)敏感的酿酒酵母(Saccharomyces cerevisiae)突变体,得到两株对诱变剂具有热条件增强(ts)敏感性的分离株。两者均归因于单个隐性核基因。突变等位基因 snm1-2(ts)主要对 HN2 表现出 ts 敏感性,而突变等位基因 snm2-1(ts)赋予 HN2、半 mustard(HN1)和 UV 的 ts 敏感性。在温度转移实验中,当在 YEPD 上于 23°C 孵育时,在暴露于诱变剂后 6 至 7 小时内,需要 SNM1 和 SNM2 的功能才能恢复,当应用 HN2 和 UV 时。用 HN1 处理后,大约需要 14 小时才能恢复 SNM2 编码的功能。这可能表明,与 HN1 诱导的损伤相比,UV 和 HN2 诱导的损伤的处理方式不同。