Mao E F, Lane L, Lee J, Miller J H
Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024, USA.
J Bacteriol. 1997 Jan;179(2):417-22. doi: 10.1128/jb.179.2.417-422.1997.
A Lac- strain of Escherichia coli that reverts by the addition of a G to a G-G-G-G-G-G sequence was used to study the proliferation of mutators in a bacterial culture. Selection for the Lac+ phenotype, which is greatly stimulated in mismatch repair-deficient strains, results in an increase in the percentage of mutators in the selected population from less than 1 per 100,000 cells to 1 per 200 cells. All the mutators detected were deficient in the mismatch repair system. Mutagenesis results in a similar increase in the percentage of mutators. Mutagenesis combined with a single selection can result in a population of more than 50% mutators when a sample of several thousand cells is grown out and selected. Mutagenesis combined with two or more successive selections can generate a population that is 100% mutator. These experiments are discussed in relation to ideas that an early step in carcinogenesis is the creation of a mutator phenotype.
利用一株通过向G - G - G - G - G - G序列中添加一个G而回复突变的大肠杆菌Lac-菌株,来研究细菌培养物中突变体的增殖情况。在错配修复缺陷菌株中,对Lac+表型的选择会受到极大刺激,这会导致所选群体中突变体的百分比从每100,000个细胞中少于1个增加到每200个细胞中1个。检测到的所有突变体在错配修复系统中均存在缺陷。诱变会导致突变体百分比出现类似的增加。当培养并挑选几千个细胞的样本时,诱变与单次选择相结合可导致突变体群体超过50%。诱变与两次或更多次连续选择相结合可产生100%为突变体的群体。结合癌症发生早期步骤是产生突变体表型这一观点对这些实验进行了讨论。