Charlier D, Roovers M, Van Vliet F, Boyen A, Cunin R, Nakamura Y, Glansdorff N, Piérard A
Research Institute of the CERIA-COOVI, Brussels, Belgium.
J Mol Biol. 1992 Jul 20;226(2):367-86. doi: 10.1016/0022-2836(92)90953-h.
The 12 genes which in E. coli K-12 constitute the arginine regulon are organized in nine transcriptional units all of which contain in their 5' non-coding region two 18 bp partially conserved imperfect palindromes (ARG boxes) which are the target sites for binding of the repressor, a hexameric protein. In vitro binding experiments with purified repressor (a gift from W. K. Maas) were performed on the operator sites of four genes, argA, argD, argF, argG, and of two operons, carAb and the bipolar argECBH cluster. A compilation of results obtained by DNase I and hydroxyl radical footprinting clearly indicates that in each case the repressor binds symmetrically to four helical turns covering adjacent pairs of boxes separated by 3 bp, but to one face of the DNA only. Methylation protection experiments bring to light major base contacts with four highly conserved G residues symmetrically distributed in four consecutive major grooves. Symmetrical contacts in the minor groove with A residues have also been identified. Stoichiometry experiments suggest that a single hexameric repressor molecule binds to a pair of adjacent ARG boxes. Although the wild-type operator consists of a pair of adjacent ARG boxes separated by 3 bp (except argR where there are only 2 bp), repressor can bind to a single box but with a greatly reduced affinity. Therefore, adjacent boxes behave co-operatively with respect to the Arg repressor binding, in the sense that the presence of one box largely stimulates the binding of the properly located second box. The optimal distance separating two boxes is 3 bp, but one bp more or less does not abolish this stimulation effect. However, it is completely abolished by the introduction of two or more additional bp unless a full helical turn is introduced. Large variations in the in vivo repression response between individual arginine genes or a wild-type gene and cognate Oc type mutants are not reflected by similar differences in the in vitro binding results where only small differences are observed. The significance of this lack of correlation is discussed.
在大肠杆菌K-12中构成精氨酸调节子的12个基因被组织成9个转录单元,所有这些转录单元在其5'非编码区都含有两个18 bp的部分保守的不完全回文序列(ARG框),它们是阻遏物(一种六聚体蛋白)的结合靶位点。用纯化的阻遏物(由W.K.马斯赠送)进行了体外结合实验,实验对象是四个基因(argA、argD、argF、argG)以及两个操纵子(carAb和双极argECBH簇)的操纵位点。通过DNA酶I和羟基自由基足迹法获得的结果汇总清楚地表明,在每种情况下,阻遏物都对称地结合到四个螺旋圈上,覆盖由3 bp隔开的相邻框对,但仅结合到DNA的一个面上。甲基化保护实验揭示了与四个高度保守的G残基的主要碱基接触,这些G残基对称分布在四个连续的大沟中。也已鉴定出在小沟中与A残基的对称接触。化学计量实验表明,单个六聚体阻遏物分子结合到一对相邻的ARG框上。尽管野生型操纵子由一对由3 bp隔开的相邻ARG框组成(除了argR,那里只有2 bp),但阻遏物可以结合到单个框上,但亲和力大大降低。因此,相邻的框在Arg阻遏物结合方面具有协同作用,即一个框的存在在很大程度上刺激了正确定位的第二个框的结合。分隔两个框的最佳距离是3 bp,但多一个或少一个bp并不会消除这种刺激作用。然而,除非引入完整的一个螺旋圈,否则引入两个或更多额外的bp会完全消除这种刺激作用。各个精氨酸基因之间或野生型基因与同源Oc型突变体之间在体内阻遏反应上的巨大差异,在体外结合结果中并未体现出类似的差异,体外结合结果中仅观察到很小的差异。讨论了这种缺乏相关性的意义。