Czarniecki D, Noel R J, Reznikoff W S
Department of Biochemistry, University of Wisconsin-Madison, 53706, USA.
J Bacteriol. 1997 Jan;179(2):423-9. doi: 10.1128/jb.179.2.423-429.1997.
The lactose (lac) operon promoter is positively regulated by the catabolite gene activator-cyclic AMP complex (CAP) that binds to the DNA located 61.5 bp upstream of the transcription start site. Between the CAP binding site and the core promoter sequence is a 13-bp sequence (from -38 to -50 [the -45 region]). The possible roles of the -45 region in determining the CAP-independent level of lac expression and in the CAP activation process were studied by isolating and characterizing random multisite mutations. Only a small percentage of mutants have dramatic effects on lac promoter activity. Among the mutations that did affect expression, a 26-fold range in lac promoter activity in vivo was observed in the CAP-independent activity. The highest level of CAP-independent lac expression (13-fold the level of the wild-type lac promoter) correlated with changes in the -40 to -45 sequence and required an intact RNA polymerase alpha subunit for in vitro expression, as expected for an upstream DNA recognition element. Mutant promoters varied in their ability to be stimulated by CAP in vivo, with levels ranging from 2-fold to the wild-type level of 22-fold. Only a change of twofold in responsiveness to CAP could be attributed to direct DNA sequence effects. The -40 to -45 sequence-dependent enhancement of promoter activity and CAP stimulation of promoter activity did not act additively. The mutant promoters also displayed other characteristics, such as the activation of nascent promoter-like activities overlapping lac P1 and, in one case, replicon-dependent changes in promoter activity.
乳糖(lac)操纵子启动子受到分解代谢基因激活蛋白 - 环磷酸腺苷复合物(CAP)的正调控,该复合物与位于转录起始位点上游61.5 bp处的DNA结合。在CAP结合位点和核心启动子序列之间是一个13 bp的序列(从 -38到 -50 [ -45区域])。通过分离和鉴定随机多位点突变,研究了 -45区域在确定lac表达的CAP非依赖性水平以及CAP激活过程中的可能作用。只有一小部分突变体对lac启动子活性有显著影响。在确实影响表达的突变中,在CAP非依赖性活性中观察到体内lac启动子活性有26倍的变化范围。CAP非依赖性lac表达的最高水平(野生型lac启动子水平的13倍)与 -40至 -45序列的变化相关,并且如上游DNA识别元件所预期的那样,体外表达需要完整的RNA聚合酶α亚基。突变启动子在体内被CAP刺激的能力各不相同,水平范围从2倍到野生型的22倍。对CAP反应性仅两倍的变化可归因于直接的DNA序列效应。启动子活性的 -40至 -45序列依赖性增强和CAP对启动子活性的刺激并非相加作用。突变启动子还表现出其他特征,例如新生的启动子样活性重叠lac P1的激活,以及在一个案例中,启动子活性的复制子依赖性变化。