Brickman T J, Ozenberger B A, McIntosh M A
Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri-Columbia 65212.
J Mol Biol. 1990 Apr 20;212(4):669-82. doi: 10.1016/0022-2836(90)90229-F.
Transcriptional linkage of the enterobactin gene cluster entCEBA (P15) was confirmed by ent-lacZ gene fusion analysis. Control sequences directing iron-regulated expression of this polycistronic message were localized to the fepB-entC bidirectional promoter region. Transcriptional initiation sites defined by primer extension analysis were located 103 base-pairs apart for the divergent fepB and entC messages. Within this divergent regulatory region, strongly consensus -35 and -10 promoter determinants and potential Fur repressor-binding sequences were identified. A vector containing divergently oriented indicator gene fusions was constructed to monitor regulatory effects of mutations within this iron-responsive control region. The fepB-entC promoter-operator elements were confirmed by mutation, using the dual gene fusion system in multicopy and low copy number states. Mutations in the -35 and -10 regions of the fepB and entC promoters that decreased their similarity to consensus resulted in reduced promoter activity. Mutations in the Fur-controlled operators reduced induction ratios (iron-deficient levels/iron-rich levels) for the respective fusion gene activities by approximately sevenfold. Although operator mutants retained some degree of inducibility, complete relief of repression was observed for double operator mutants, suggesting that only minor regulatory influence is exerted by Fur occupation of the opposing operator site. DNase I footprinting experiments were performed to characterize the sequence-specific Fur interactions at the operator sequences. At the fepB operator, a 31 base-pair Fur-protected region was identified, corresponding to positions -19 to +12 with respect to the transcriptional start site. Similarly, Fur protected a 31 base-pair region in entC, corresponding to positions +1 to +31 in the message. A contiguous and sequentially occupied secondary Fur-binding site in entC was protected at higher Fur concentrations, extending the protected region to +49, and sequestering the putative Shine-Dalgarno sequence. Operator positional effects and co-operativity are discussed.
通过肠杆菌素基因融合分析证实了肠杆菌素基因簇entCEBA(P15)的转录连锁。指导该多顺反子信息铁调节表达的控制序列定位于fepB-entC双向启动子区域。通过引物延伸分析确定的转录起始位点,对于fepB和entC的不同转录信息而言,相距103个碱基对。在这个不同的调控区域内,鉴定出了高度一致的-35和-10启动子决定簇以及潜在的Fur阻遏物结合序列。构建了一个含有反向指示基因融合体的载体,以监测该铁反应控制区域内突变的调控作用。利用多拷贝和低拷贝数状态下的双基因融合系统,通过突变证实了fepB-entC启动子-操纵子元件。fepB和entC启动子-35和-10区域内与共有序列相似性降低的突变导致启动子活性降低。Fur控制的操纵子中的突变使各自融合基因活性的诱导率(缺铁水平/富铁水平)降低了约7倍。虽然操纵子突变体保留了一定程度的诱导性,但对于双操纵子突变体观察到了阻遏的完全解除,这表明Fur占据相反的操纵子位点仅产生轻微的调控影响。进行了DNase I足迹实验,以表征操纵子序列处序列特异性的Fur相互作用。在fepB操纵子处,鉴定出一个31个碱基对的Fur保护区域,相对于转录起始位点对应于-19至+12位。同样,Fur在entC中保护了一个31个碱基对的区域,对应于转录信息中的+1至+31位。在较高的Fur浓度下,entC中一个连续且依次占据的二级Fur结合位点受到保护,将保护区域扩展至+49,并隔离了假定的Shine-Dalgarno序列。讨论了操纵子位置效应和协同性。