Godbout R, Ingram R, Tilghman S M
Mol Cell Biol. 1986 Feb;6(2):477-87. doi: 10.1128/mcb.6.2.477-487.1986.
Three enhancer elements spanning a distance of 7 kilobases have been found at the 5' end of the alpha-fetoprotein (AFP) gene. These elements were identified by transient expression assay after the introduction of a modified mouse AFP gene with variable amounts of 5' flanking sequence into a human hepatoma cell line, Hep G2. These regulatory elements function in a position-independent and orientation-independent manner that is typical of enhancers. All three elements will stimulate transcription from the promoter of the herpes simplex virus thymidine kinase gene. In Hep G2 cells, transcriptional activation from the heterologous promoter was approximately 25- to 50-fold higher than the basal levels obtained in the absence of AFP enhancer elements. In HeLa cells, the increase in thymidine kinase gene transcription varied from 6- to 14-fold, indicating that the enhancer elements exhibit some cell type specificity. Deletion analysis of the region proximal to the AFP transcription initiation site identified an essential region between 85 and 52 bases upstream of the site of initiation of transcription whose removal resulted in almost complete extinction of transcriptional activity. This region, which has been shown to be dispensable for transcription in HeLa cells, defines a second tissue-specific regulatory region in the gene.
在甲胎蛋白(AFP)基因的5'端发现了三个跨越7千碱基距离的增强子元件。通过将带有不同数量5'侧翼序列的修饰小鼠AFP基因导入人肝癌细胞系Hep G2后进行瞬时表达分析,鉴定出了这些元件。这些调控元件以增强子典型的位置独立和方向独立的方式发挥作用。所有这三个元件都将刺激单纯疱疹病毒胸苷激酶基因启动子的转录。在Hep G2细胞中,来自异源启动子的转录激活比在没有AFP增强子元件时获得的基础水平高约25至50倍。在HeLa细胞中,胸苷激酶基因转录的增加幅度在6至14倍之间,这表明增强子元件表现出一定的细胞类型特异性。对AFP转录起始位点近端区域的缺失分析确定了转录起始位点上游85至52个碱基之间的一个必需区域,去除该区域会导致转录活性几乎完全消失。该区域已被证明在HeLa细胞中对于转录是可有可无的,它定义了该基因中的第二个组织特异性调控区域。