Oh M, Chai S H, Wee S
Department of Genetic Engineering, Hallym University, Chunchon, Korea.
Mol Cells. 1999 Oct 31;9(5):517-25.
Fur (ferric uptake regulation) binding fragments were isolated by in vitro binding of purified Fur protein with Sau3AI-digested genomic DNA fragments. The Fur-bound DNA fragments were filtered on nitrocellulose paper, isolated, cloned, and sequenced. The protein binding was confirmed by gel retardation assay for five DNA fragments. The sequence data were used to identify the genes by comparison with the GenBank data. The proposed Fur binding regions lie on or near the putative promoter regions of marAB (multiple antibiotic resistance), pyrC (dihydroorotase), mreB (mecillinam resistance) and an unidentified gene (ecouw93) near argI and in the middle of the treBC (trehalose permease enzyme II) coding region. The proposed Fur binding sites of the known iron regulating operators including the genes of this work are AAT(pyrimidine) and A(purine)TT. The two conserved sequences are 10 bases apart and palindromic to each other, which might suggest the classical pattern of protein binding toward one side of the DNA in contrast to the concept of the Fur protein wrapping around the DNA.
通过将纯化的Fur蛋白与经Sau3AI酶切的基因组DNA片段进行体外结合,分离出Fur(铁摄取调节)结合片段。将与Fur结合的DNA片段在硝酸纤维素纸上进行过滤、分离、克隆和测序。通过凝胶阻滞试验对五个DNA片段进行了蛋白质结合确认。通过与GenBank数据进行比较,利用序列数据鉴定基因。推测的Fur结合区域位于marAB(多重抗生素抗性)、pyrC(二氢乳清酸酶)、mreB(美西林抗性)的假定启动子区域上或附近,以及argI附近和treBC(海藻糖通透酶II)编码区域中间的一个未鉴定基因(ecouw93)附近。包括本研究基因在内的已知铁调节操纵子的推测Fur结合位点为AAT(嘧啶)和A(嘌呤)TT。这两个保守序列相隔10个碱基且彼此呈回文结构,这可能表明蛋白质与DNA一侧结合的经典模式,与Fur蛋白环绕DNA的概念形成对比。