Siegel E C, Bryson V
J Bacteriol. 1967 Jul;94(1):38-47. doi: 10.1128/jb.94.1.38-47.1967.
An azaserine-resistant derivative of Escherichia coli B/UV, AZA/R(1), was found to carry a mutator gene. This gene, designated mutS1, was mapped by means of conjugation and P1kc-mediated transduction. The mutS1 gene was cotransduced with argB at a frequency of 2.4%; the gene order in this region of the chromosome is thy argB mutS1. To determine whether a relationship commonly exists between azaserine resistance and the mutator property, 12 additional azaserine-resistant derivatives of B/UV were developed and tested for the mutator phenotype. None of the twelve was a mutator strain. The level of azaserine resistance was not increased over that of the recipient parent when mutS1 was transduced to an azaserine-susceptible strain. Reversion studies indicated that mutS1 induced adenosine-ribosylthymine to guanosine-cytidine and guanosine-cytidine to adenosine-ribosylthymine transitions. Because such mutational changes are suppressible with deoxynucleosides when induced by base analogues, an attempt was made to suppress the mutator activity of mutS1 by the addition of deoxyribonucleosides to the medium. No suppression was found. Recombinants were prepared containing mutS1 and the Treffers mutator gene of E. coli K-12. The effect of the mutator genes appears to be additive.
发现大肠杆菌B/UV的一种氮杂丝氨酸抗性衍生物AZA/R(1)携带一个突变基因。这个基因被命名为mutS1,通过接合和P1kc介导的转导进行定位。mutS1基因与argB共转导的频率为2.4%;染色体该区域的基因顺序是thy argB mutS1。为了确定氮杂丝氨酸抗性与突变特性之间是否普遍存在关联,又培育了12种B/UV的氮杂丝氨酸抗性衍生物,并检测其突变体表型。这12种衍生物中没有一个是突变菌株。当mutS1被转导到一个对氮杂丝氨酸敏感的菌株时,其氮杂丝氨酸抗性水平并没有比受体亲本提高。回复突变研究表明,mutS1诱导腺苷核糖胸腺嘧啶向鸟苷胞嘧啶以及鸟苷胞嘧啶向腺苷核糖胸腺嘧啶的转变。因为当由碱基类似物诱导时,这种突变变化可用脱氧核苷抑制,所以尝试通过向培养基中添加脱氧核糖核苷来抑制mutS1的突变活性。但未发现抑制作用。制备了含有mutS1和大肠杆菌K - 12的Treffers突变基因的重组体。这些突变基因的作用似乎是累加的。