Tardat B, Touati D
Institut Jacques Monod, CNRS, Université Paris 7, France.
Mol Microbiol. 1993 Jul;9(1):53-63. doi: 10.1111/j.1365-2958.1993.tb01668.x.
Manganese superoxide dismutase (the sodA gene product) in Escherichia coli, is negatively regulated by two global regulators, ArcA (aerobic respiration control) and Fur (ferric uptake regulation), coupling its expression to aerobic metabolism and the intracellular iron pool. Footprinting analyses were carried out on the sodA promoter region with purified Fur protein and with ArcA protein overproduced in crude extracts. ArcA is able to bind in vitro in the absence of the in vivo triggering signal. The binding occurs in one step and study of contacts within the operator sequence reveals binding on one side of the double helix. The DNA protection extends to a much larger region (about 65 bp) than would be expected for a 27 kDa protein, suggesting polymerization. Both Fur and ArcA footprints encompass the -35 and -10 promoter region and there is considerable overlap of their binding sequences, in agreement with in vivo results suggesting that either regulator alone can block sodA transcription. Furthermore, competition experiments show that Fur and ArcA binding to the sodA promoter are mutually exclusive and that ArcA can easily displace Fur, but not vice versa. The biological significance of this in vitro behaviour is discussed.
大肠杆菌中的锰超氧化物歧化酶(sodA基因产物)受两种全局调节因子ArcA(有氧呼吸控制)和Fur(铁摄取调节)的负调控,使其表达与有氧代谢和细胞内铁池相关联。利用纯化的Fur蛋白和在粗提物中过量表达的ArcA蛋白,对sodA启动子区域进行了足迹分析。在没有体内触发信号的情况下,ArcA能够在体外结合。结合以一步进行,对操纵序列内接触的研究揭示其在双螺旋的一侧结合。DNA保护延伸到比预期的27 kDa蛋白更大的区域(约65 bp),表明存在聚合作用。Fur和ArcA的足迹都包含-35和-10启动子区域,并且它们的结合序列有相当大的重叠,这与体内结果一致,表明单独任何一种调节因子都可以阻断sodA转录。此外,竞争实验表明,Fur和ArcA与sodA启动子的结合是相互排斥的,并且ArcA可以轻易取代Fur,但反之则不然。本文讨论了这种体外行为的生物学意义。