Aronson J F, Stamato T D
Mutat Res. 1987 Apr;177(2):277-81. doi: 10.1016/0027-5107(87)90011-x.
Treatment of G1-synchronized mammalian cells with mutagenic agents which act on one strand of the DNA at a given site would be expected to produce colonies containing both mutant and wild-type cells (mosaic). We have observed that in addition to mosaic colonies, G1-synchronized Chinese hamster ovary cells which had been treated with the single-strand mutagen ethyl methanesulfonate (EMS), produced colonies in which all the cells lacked glucose-6-phosphate dehydrogenase activity. These completely mutant (pure) colonies could be derived from a potentially mosaic colony by the "death" of the wild-type cell after the first cell division, leaving only the glucose-6-phosphate dehydrogenase (G6PD)-deficient cell to grow into a colony (lethal sectoring). Using time-lapse photography to analyze cell lineages after EMS treatment, we find that cell lysis, cell release, cell migration, or proliferative failure of one lineage at the 2-cell stage accounts for only 20-25% of the pure mutant colonies observed. This result suggests that in the Chinese hamster cell there exists a mutational mechanism which fixes the mutation in both strands of the DNA before the next replication cycle following EMS treatment.
用作用于特定位点单链DNA的诱变剂处理G1期同步化的哺乳动物细胞,预期会产生同时含有突变细胞和野生型细胞的菌落(嵌合体)。我们观察到,除了嵌合菌落外,用单链诱变剂甲磺酸乙酯(EMS)处理过的G1期同步化的中国仓鼠卵巢细胞还产生了所有细胞都缺乏葡萄糖-6-磷酸脱氢酶活性的菌落。这些完全突变(纯合)的菌落可能是由潜在的嵌合菌落衍生而来,即在第一次细胞分裂后野生型细胞“死亡”,只留下葡萄糖-6-磷酸脱氢酶(G6PD)缺陷型细胞生长成一个菌落(致死性扇形化)。通过延时摄影分析EMS处理后的细胞谱系,我们发现细胞裂解、细胞释放、细胞迁移或在2细胞期一个谱系的增殖失败仅占所观察到的纯合突变菌落的20%-25%。这一结果表明,在中国仓鼠细胞中存在一种突变机制,该机制在EMS处理后的下一个复制周期之前将突变固定在DNA的两条链上。