Belas R, Mileham A, Simon M, Silverman M
J Bacteriol. 1984 Jun;158(3):890-6. doi: 10.1128/jb.158.3.890-896.1984.
Coliphage P1 was used to transduce derivatives of transposons Tn5 and mini-Mu into marine Vibrio spp. Transposon Tn5 encoding tetracycline resistance (Tn5-132) was used to isolate mutants of Vibrio harveyi defective in genes for bioluminescence (lux). Insertion of transposon Tn5-132 into the lux gene region was demonstrated by intraspecific transduction with phage hv-1 and by Southern blot hybridization. Transposon mini-Mu, modified to specify tetracycline resistance, was employed to mutagenize genes for lateral flagella synthesis of Vibrio parahaemolyticus. Mini-Mu contains the lacZ structural gene, and transposition results in transcriptional fusion of Vibrio genes with the transposon lacZ gene. Thus, in these fusions, lacZ expression was proportional to the level of transcription of the target gene. Regulation of lateral flagella gene expression was studied in vivo by measuring beta-galactosidase activity, and conditions which activate transcription of these genes were identified. A method for gene cloning with transposon-induced mutations is discussed.
用大肠杆菌噬菌体P1将转座子Tn5和mini-Mu的衍生物转导到海洋弧菌属细菌中。编码四环素抗性的转座子Tn5(Tn5-132)被用于分离哈维氏弧菌中与生物发光(lux)相关基因缺陷的突变体。通过噬菌体hv-1的种内转导和Southern印迹杂交证明了转座子Tn5-132插入到了lux基因区域。经修饰以赋予四环素抗性的转座子mini-Mu被用于对副溶血性弧菌的侧鞭毛合成相关基因进行诱变。Mini-Mu含有lacZ结构基因,转座导致弧菌基因与转座子lacZ基因发生转录融合。因此,在这些融合中,lacZ表达与靶基因的转录水平成正比。通过测量β-半乳糖苷酶活性在体内研究了侧鞭毛基因表达的调控,并确定了激活这些基因转录的条件。讨论了一种利用转座子诱导突变进行基因克隆的方法。