Gustavson Mark D, Crawford Howard C, Fingleton Barbara, Matrisian Lynn M
Department of Cancer Biology, Vanderbilt University, Nashville, TN 37232-6840, USA.
Mol Carcinog. 2004 Nov;41(3):125-39. doi: 10.1002/mc.20049.
The matrix metalloproteinase-7 (MMP-7) gene is a target of beta-catenin transactivation. Expression of the T-cell factor, Lef-1, enhances transcriptional activation of the human MMP-7 promoter by beta-catenin, but represses activation of the mouse MMP-7 promoter, both activities through consensus Tcf binding sites. The mouse promoter has a single Tcf binding element (mTBE) located downstream of the transcriptional start site, while the human promoter has two Tcf binding elements (hTBE1, hTBE2), both located upstream of the transcriptional start. hTBE1 and hTBE2 also differ in sequence from mTBE. Here we demonstrate that positioning of mTBE, upstream or downstream of the transcriptional start site dictated whether Lef-1 functioned as an activator or repressor, respectively. Sequence differences between mTBE and hTBE sites determined the potency of these activities, with hTBE sites being weaker. Mutational analysis of mTBE showed that increased Lef-1 activity mapped to G . C base pairings at 5' and 3' ends, and correlated with a threefold increase in Lef-1 binding affinity in vitro. Heterologous promoters with high affinity binding sites were 115-fold more responsive to beta-catenin than those with low affinity sites. Converting low affinity Tcf binding sites to high affinity sites increased beta-catenin responsiveness of the mouse and human promoters by 2-3 fold, and ectopic expression of Lef-1 increased beta-catenin responsiveness for promoters with low affinity binding sequences. We concluded that sequence and position of Tcf binding sites can determine the extent of beta-catenin-Lef-1 responsiveness for beta-catenin target genes.
基质金属蛋白酶-7(MMP-7)基因是β-连环蛋白转录激活的靶点。T细胞因子Lef-1的表达增强了β-连环蛋白对人MMP-7启动子的转录激活作用,但抑制了小鼠MMP-7启动子的激活作用,这两种作用均通过共有Tcf结合位点实现。小鼠启动子在转录起始位点下游有一个单一的Tcf结合元件(mTBE),而人启动子有两个Tcf结合元件(hTBE1、hTBE2),均位于转录起始位点上游。hTBE1和hTBE2在序列上也与mTBE不同。在这里,我们证明mTBE在转录起始位点上游或下游的定位分别决定了Lef-1是作为激活剂还是抑制剂发挥作用。mTBE和hTBE位点之间的序列差异决定了这些作用的效力,hTBE位点的效力较弱。对mTBE的突变分析表明,Lef-1活性的增加定位于5'和3'末端的G.C碱基对,并且与体外Lef-1结合亲和力增加三倍相关。具有高亲和力结合位点的异源启动子对β-连环蛋白的反应性比具有低亲和力位点的启动子高115倍。将低亲和力Tcf结合位点转换为高亲和力位点可使小鼠和人启动子对β-连环蛋白的反应性提高2-3倍,并且Lef-1的异位表达增加了具有低亲和力结合序列的启动子对β-连环蛋白的反应性。我们得出结论,Tcf结合位点的序列和位置可以决定β-连环蛋白靶基因对β-连环蛋白-Lef-1反应的程度。