Wood T I, Griffith K L, Fawcett W P, Jair K W, Schneider T D, Wolf R E
Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.
Mol Microbiol. 1999 Nov;34(3):414-30. doi: 10.1046/j.1365-2958.1999.01598.x.
SoxS is the direct transcriptional activator of the member genes of the Escherichia coli superoxide regulon. At class I SoxS-dependent promoters, e.g. zwf and fpr, whose SoxS binding sites ('soxbox') lie upstream of the -35 region of the promoter, activation requires the C-terminal domain of the RNA polymerase alpha-subunit, while at class II SoxS-dependent promoters, e.g. fumC and micF, whose binding sites overlap the -35 region, activation is independent of the alpha-CTD. To determine whether SoxS activation of its class I promoters shows the same helical phase-dependent spacing requirement as class I promoters activated by catabolite gene activator protein, we increased the 7 bp distance between the 20 bp zwf soxbox and the zwf -35 promoter hexamer by 5 bp and 11 bp, and we decreased the 15 bp distance between the 20 bp fpr soxbox and the fpr -35 promoter hexamer by the same amounts. In both cases, displacement of the binding site by a half or full turn of the DNA helix prevented transcriptional activation. With constructs containing the binding site of one gene fused to the promoter of the other, we demonstrated that the positional requirements are a function of the specific binding site, not the promoter. Supposing that opposite orientation of the SoxS binding site at the two promoters might account for the positional requirements, we placed the zwf and fpr soxboxes in the reverse orientation at the various positions upstream of the promoters and determined the effect of orientation on transcription activation. We found that reversing the orientation of the zwf binding site converts its positional requirement to that of the fpr binding site in its normal orientation, and vice versa. Analysis by molecular information theory of DNA sequences known to bind SoxS in vitro is consistent with the opposite orientation of the zwf and fpr soxboxes.
SoxS是大肠杆菌超氧化物调节子成员基因的直接转录激活因子。在I类SoxS依赖型启动子(如zwf和fpr)中,其SoxS结合位点(“soxbox”)位于启动子-35区上游,激活需要RNA聚合酶α亚基的C末端结构域;而在II类SoxS依赖型启动子(如fumC和micF)中,其结合位点与-35区重叠,激活不依赖于α-CTD。为了确定SoxS对其I类启动子的激活是否显示出与分解代谢基因激活蛋白激活的I类启动子相同的螺旋相位依赖性间距要求,我们将20 bp的zwf soxbox与zwf -35启动子六聚体之间的7 bp距离增加了5 bp和11 bp,并将20 bp的fpr soxbox与fpr -35启动子六聚体之间的15 bp距离减少了相同的量。在这两种情况下,DNA螺旋半圈或一圈的结合位点位移都阻止了转录激活。对于含有一个基因的结合位点与另一个基因的启动子融合的构建体,我们证明位置要求是特定结合位点的函数,而不是启动子的函数。假设两个启动子处SoxS结合位点的相反方向可能解释位置要求,我们将zwf和fpr soxbox以相反方向置于启动子上游的不同位置,并确定方向对转录激活的影响。我们发现,反转zwf结合位点的方向会将其位置要求转换为fpr结合位点正常方向的要求,反之亦然。对已知在体外结合SoxS的DNA序列进行分子信息理论分析,与zwf和fpr soxbox的相反方向一致。