Tanaka S, Kaytes P, Kurkinen M
Department of Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway 08854.
J Biol Chem. 1993 Apr 25;268(12):8862-70.
Expression of collagen IV genes is developmentally regulated and cell type-specific. To identify transcriptional control elements for the mouse alpha 2(IV) collagen gene, several promoter constructs were transiently transfected into mouse PYS-2 (parietal yolk sac) cells. Within the 5.5-kb (kilobase) upstream and 8.5-kb downstream sequences from the transcription start site, we have identified several regulatory active regions. Here, we report characterization of the most proximal 0.3-kb enhancer found at 4.5-kb upstream of the alpha 2(IV) collagen gene. This enhancer is transcriptionally active in cells that make collagen IV such as PYS-2 cells and differentiated F9 cells, but has little if any activity in cells that do not make collagen IV including NIH 3T3 cells and undifferentiated F9 embryonal carcinoma stem cells. This enhancer, linked to the herpes simplex virus TK gene promoter, confers a cell type-specific and differentiation-induced expression on the TK gene as well. Mutational and 5' and 3' deletion analysis demonstrate that this enhancer activity requires two identical response elements (GAACAAT) present in the 0.3-kb enhancer sequence. In gel shift assay, the GAACAAT element forms a complex that is specific for cells that make collagen IV.
IV型胶原蛋白基因的表达受发育调控且具有细胞类型特异性。为了鉴定小鼠α2(IV)胶原蛋白基因的转录控制元件,将几种启动子构建体瞬时转染到小鼠PYS-2(壁层卵黄囊)细胞中。在转录起始位点上游5.5千碱基(kb)和下游8.5 kb的序列范围内,我们鉴定出了几个调控活性区域。在此,我们报道了在α2(IV)胶原蛋白基因上游4.5 kb处发现的最接近的0.3 kb增强子的特征。该增强子在产生IV型胶原蛋白的细胞如PYS-2细胞和分化的F9细胞中具有转录活性,但在不产生IV型胶原蛋白的细胞包括NIH 3T3细胞和未分化的F9胚胎癌干细胞中几乎没有活性。该增强子与单纯疱疹病毒TK基因启动子相连,也赋予TK基因细胞类型特异性和分化诱导表达。突变分析以及5'和3'缺失分析表明,这种增强子活性需要0.3 kb增强子序列中存在的两个相同的反应元件(GAACAAT)。在凝胶迁移试验中,GAACAAT元件形成一种复合物,该复合物对产生IV型胶原蛋白的细胞具有特异性。