Hwung Y P, Crowe D T, Wang L H, Tsai S Y, Tsai M J
Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.
Mol Cell Biol. 1988 May;8(5):2070-7. doi: 10.1128/mcb.8.5.2070-2077.1988.
Band-shifting and DNase I-footprinting assays have been used to study the trans-acting factor(s) binding to an important promoter element (-53 to -46 relative to the transcription start) of the rat insulin II gene. A binding activity which footprints a region between -60 and -40 was found in both HIT, a hamster insulinoma cell line, and HeLa cells. A mutation within this region which drastically decreases promoter activity in vivo also greatly reduces binding activity in vitro. This binding activity was purified from HeLa cells and identified by competition and renaturation analyses as being the same as the COUP (chicken ovalbumin upstream promoter) transcription factor, a DNA-binding protein required for efficient transcription of the ovalbumin gene in vitro. Interestingly, the binding sequences of the COUP transcription factor in the ovalbumin and the insulin promoters have only limited similarities.
凝胶迁移实验和DNA酶I足迹实验已被用于研究与大鼠胰岛素II基因一个重要启动子元件(相对于转录起始点为-53至-46)结合的反式作用因子。在仓鼠胰岛素瘤细胞系HIT和HeLa细胞中均发现了一种结合活性,其足迹位于-60至-40区域之间。该区域内的一个突变在体内会大幅降低启动子活性,在体外也会极大地降低结合活性。这种结合活性从HeLa细胞中纯化出来,并通过竞争和复性分析鉴定为与COUP(鸡卵清蛋白上游启动子)转录因子相同,COUP转录因子是一种DNA结合蛋白,在体外是卵清蛋白基因高效转录所必需的。有趣的是,COUP转录因子在卵清蛋白和胰岛素启动子中的结合序列仅有有限的相似性。