Rosenberg M, Chepelinsky A B, McKenney K
Science. 1983 Nov 18;222(4625):734-9. doi: 10.1126/science.6356355.
Prokaryotic gene control signals can be isolated, compared, and characterized by precise fusion in vitro to the Escherichia coli galactokinase gene (galK), which provides both a simple assay and genetic selection. This recombinant galK fusion vector system was applied to the study of promoters and terminators recognized by the Escherichia coli RNA polymerase. Three promoters created by mutation from DNA sequences having no promoter function were characterized. Mutations that inactivate promoter function were selected, structurally defined, and functionally analyzed. Similarly, transcription termination was examined, and mutations affecting terminator function were isolated and characterized.
原核基因控制信号可以通过在体外与大肠杆菌半乳糖激酶基因(galK)进行精确融合来分离、比较和表征,该基因提供了一种简单的检测方法和遗传筛选手段。这种重组galK融合载体系统被应用于研究大肠杆菌RNA聚合酶识别的启动子和终止子。对由无启动子功能的DNA序列突变产生的三个启动子进行了表征。选择了使启动子功能失活的突变,对其进行了结构定义和功能分析。同样,对转录终止进行了研究,分离并表征了影响终止子功能的突变。