Lee David J, Busby Stephen J W, Lloyd Georgina S
School of Biosciences, the University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom.
J Biol Chem. 2003 Dec 26;278(52):52944-52. doi: 10.1074/jbc.M308300200. Epub 2003 Oct 6.
The C-terminal domain of the alpha subunit (alphaCTD) of bacterial RNA polymerase plays an important role in promoter recognition. It is known that alphaCTD binds to the DNA minor groove at different locations at different promoters via a surface-exposed determinant, the 265 determinant. Here we describe experiments that permit us to determine the location and orientation of binding of alphaCTD at any promoter. In these experiments, a DNA cleavage reagent is attached to specific locations on opposite faces of the RNA polymerase alpha subunit. After incorporation of the tagged alpha subunits into holo-RNA polymerase, patterns of DNA cleavage due to the reagent are determined in open complexes. The locations of DNA cleavage due to the reagent attached at different positions allow the position and orientation of alphaCTD to be deduced. Here we present data from experiments with simple Escherichia coli promoters that are activated by the cyclic AMP receptor protein.
细菌RNA聚合酶α亚基的C末端结构域(αCTD)在启动子识别中起重要作用。已知αCTD通过一个表面暴露的决定簇,即265决定簇,在不同启动子的不同位置与DNA小沟结合。在此,我们描述了一些实验,这些实验使我们能够确定αCTD在任何启动子上的结合位置和方向。在这些实验中,一种DNA切割试剂被连接到RNA聚合酶α亚基相对面上的特定位置。在将标记的α亚基掺入全酶RNA聚合酶后,在开放复合物中确定由该试剂引起的DNA切割模式。由于连接在不同位置的试剂导致的DNA切割位置,使得αCTD的位置和方向得以推断。在此,我们展示了用由环磷酸腺苷受体蛋白激活的简单大肠杆菌启动子进行实验得到的数据。