Cabezón T, Faelen M, De Wilde M, Bollen A, Thomas R
Mol Gen Genet. 1975;137(2):125-9. doi: 10.1007/BF00341678.
Streptomycin or spectinomycin treatment of an E. coli strain, carrying the strR and spcR alleles on the chromosome and the wild-type (sensitive) alleles on the episome, selects for inactivation of the relevant sensitive allele. After Mu induced mutagenesis, in the absence of selection against extended deletions upon the episome, a large proportion of stro mutants are also spco, and vice versa. However, when markers flanking the strA and spcA gene cluster are simultaneously selected, effectively eliminating long deletions, the majority of stro mutants continue to express the spcs allele, and vice versa. Insofar as inactivation after Mu treatment is due to prophage insertion within or proximal to the genes in question, this result indicates that the genes strA and spcA are not parts of a single operon. In virtue of the high frequency of extended deletions observed in the absence of suitable counter-selection, we must place a word of caution upon the use of phage Mu-1 as a means of isolating polar mutations and defining transcriptional units.
用链霉素或壮观霉素处理一种大肠杆菌菌株,该菌株在染色体上携带strR和spcR等位基因,在附加体上携带野生型(敏感)等位基因,会选择使相关敏感等位基因失活。在Mu诱导诱变后,在没有针对附加体上延伸缺失进行选择的情况下,很大比例的str o突变体也是spc o,反之亦然。然而,当同时选择strA和spcA基因簇两侧的标记,有效消除长缺失时,大多数str o突变体继续表达spc s等位基因,反之亦然。就Mu处理后的失活是由于原噬菌体插入相关基因内部或附近而言,这一结果表明strA和spcA基因不是单个操纵子的组成部分。鉴于在没有合适的反选择时观察到延伸缺失的频率很高,我们必须对使用噬菌体Mu-1作为分离极性突变和定义转录单位的手段持谨慎态度。