Tu A Y, Wolfbauer G, Albers J J
Department of Medicine, Northwest Lipid Research Laboratories, University of Washington, Seattle 98103, USA.
Biochem Biophys Res Commun. 1995 Dec 26;217(3):705-11. doi: 10.1006/bbrc.1995.2830.
We have identified the functional promoter region of the human phospholipid transfer protein gene. Primer extension analysis indicates multiple sites for transcription initiation. Sequence analysis reveals that the promoter consists of TATA box, high GC region, and several consensus sequences for the potential binding of transcription factors. To assay promoter activity, DNA fragments with various lengths of the 5'-flanking region were fused upstream to the luciferase gene and transfected into HepG2, COS-7, and CHO cells. A minimal promoter of 159 base pairs between -230 and -72 relative to the first transcriptional initiation site is responsible for the full activity. Two motifs, Sp1 and AP-2, are located within this area. It may suggest that the PLTP promoter activity relies primarily on the putative cis-elements in the functional region.
我们已经鉴定出人类磷脂转运蛋白基因的功能启动子区域。引物延伸分析表明存在多个转录起始位点。序列分析显示该启动子由TATA盒、高GC区域以及几个潜在转录因子结合的共有序列组成。为了检测启动子活性,将具有不同长度5'侧翼区域的DNA片段融合到荧光素酶基因上游,并转染到HepG2、COS-7和CHO细胞中。相对于第一个转录起始位点,在-230至-72之间的159个碱基对的最小启动子负责全部活性。两个基序,即Sp1和AP-2,位于该区域内。这可能表明PLTP启动子活性主要依赖于功能区域中假定的顺式元件。