Gunther M, Frebourg T, Laithier M, Fossar N, Bouziane-Ouartini M, Lavialle C, Brison O
Laboratoire de Génétique Oncologique, URA 1967 CNRS, Institut Gustave Roussy, Villejuif, France.
Mol Cell Biol. 1995 May;15(5):2490-9. doi: 10.1128/MCB.15.5.2490.
Clones of cells tumorigenic or nontumorigenic in nude mice have been previously isolated from the SW613-S human colon carcinoma cell line. We have already reported that tumorigenic cells overexpress the cytokeratin 18 (K18) gene in comparison with nontumorigenic cells and that this difference is mainly due to a transcriptional regulation. We now report that a 2,532-bp cloned human K18 gene promoter drives the differential expression of a reporter gene in a transient assay. A 62-bp minimal K18 promoter (TATA box and initiation site) has a low but differential activity. Analysis of deletion and substitution mutants as well as hybrid SV40-K18 promoters and reconstructed K18 promoters indicated that an important element for the activity of the K18 promoter is a high-affinity binding site for transcription factor Sp1 located just upstream of the TATA box. This Sp1 binding element, as well as the intron 1 enhancer element, stimulates the basal activity of the minimal promoter through mechanisms that maintain the differential activity. Gel shift assays and the use of an anti-Sp1 antibody have shown that both tumorigenic and nontumorigenic SW613-S cells contain three factors able to bind to the Sp1 binding element site and that one of them is Sp1. A hybrid GAL4-Sp1 protein transactivated to comparable extents in tumorigenic and nontumorigenic cells a reconstructed K18 promoter containing GAL4 binding sites and therefore without altering its differential behavior. These results indicate that the Sp1 transcription factor is involved in the overexpression of the K18 gene in tumorigenic SW613-S cells through its interaction with a component of the basal transcription machinery.
此前已从SW613-S人结肠癌细胞系中分离出在裸鼠体内具有致瘤性或无致瘤性的细胞克隆。我们已经报道,与无致瘤性细胞相比,致瘤性细胞中细胞角蛋白18(K18)基因过表达,且这种差异主要归因于转录调控。我们现在报道,一个2532 bp的克隆人K18基因启动子在瞬时分析中驱动报告基因的差异表达。一个62 bp的最小K18启动子(TATA盒和起始位点)具有低但有差异的活性。对缺失和替代突变体以及杂交SV40-K18启动子和重建的K18启动子的分析表明,K18启动子活性的一个重要元件是位于TATA盒上游的转录因子Sp1的高亲和力结合位点。这个Sp1结合元件以及内含子1增强子元件通过维持差异活性的机制刺激最小启动子的基础活性。凝胶迁移分析和抗Sp1抗体的使用表明,致瘤性和无致瘤性的SW613-S细胞都含有三种能够与Sp1结合元件位点结合的因子,其中之一是Sp1。一种杂交GAL4-Sp1蛋白在致瘤性和无致瘤性细胞中以相当的程度反式激活含有GAL4结合位点因此不改变其差异行为的重建K18启动子。这些结果表明,Sp1转录因子通过与基础转录机制的一个组分相互作用参与致瘤性SW613-S细胞中K18基因的过表达。