Cui Y, Midkiff M A, Wang Q, Calvo J M
Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853, USA.
J Biol Chem. 1996 Mar 22;271(12):6611-7. doi: 10.1074/jbc.271.12.6611.
Lrp (Leucine-responsive regulatory protein) regulates the expression of a number of operons in Escherichia coli. A recent study of DNA sequences recognized by Lrp established the consensus as a 15-bp sequence, YAGHAWATTWTDCTR (Y = C/T, H = "not G," W = A/T, D ="not C," R = A/G) (Cui, Y., Wang, Q., Stormo, G. D., and Calvo, J. M. (1995) J. Bacteriol. 177, 4872-4880). Here we report the stoichiometry of Lrp binding (an Lrp dimer binds to a single binding site) and studies that define the minimal length of DNA required for binding. A double-stranded 15 mer having a sequence that closely matches the consensus does not show measurable binding to Lrp. One or two base pairs of DNA flanking each end are not sufficient for binding, but constructs having 3-5 additional base pairs (21 mer) show relatively strong binding. Single-stranded flanking DNA also contributes to strong binding. The extent of the contribution to binding is dependent upon whether the single strand is on the left or right of the double-stranded region and whether the polarity of the single-stranded DNA is 5' to 3' or 3' to 5'.
Lrp(亮氨酸响应调节蛋白)调控大肠杆菌中多个操纵子的表达。最近一项关于Lrp识别的DNA序列的研究确定共有序列为15个碱基对的序列,即YAGHAWATTWTDCTR(Y = C/T,H = “非G”,W = A/T,D = “非C”,R = A/G)(崔毅、王强、斯托莫、卡尔沃,(1995年)《细菌学杂志》177卷,4872 - 4880页)。在此我们报告Lrp结合的化学计量关系(一个Lrp二聚体结合一个单一结合位点)以及确定结合所需最小DNA长度的研究。一个具有与共有序列紧密匹配的序列的双链15聚体未显示出与Lrp的可测量结合。两端各有一两个碱基对的DNA不足以实现结合,但具有额外3 - 5个碱基对(21聚体)的构建体显示出相对较强的结合。单链侧翼DNA也有助于实现强结合。其对结合的贡献程度取决于单链是在双链区域的左侧还是右侧,以及单链DNA的极性是5'到3'还是3'到5'。