Ishii S, Kadonaga J T, Tjian R, Brady J N, Merlino G T, Pastan I
Science. 1986 Jun 13;232(4756):1410-3. doi: 10.1126/science.3012774.
Members of the ras gene family encode proteins that when overproduced or mutated can transform immortalized mammalian cells. It is therefore important to understand the mechanisms by which the ras genes are regulated. The promoter region of the human Harvey ras proto-oncogene c-Ha-ras1 initiates RNA transcription at multiple sites and contains repeated copies of the hexanucleotide GGGCGG and its inverted complement CCGCCC, referred to as GC boxes. These GC boxes consist of sequences identical to those found in the SV40 early promoter, where the human cellular transcriptional factor Sp1 binds. Footprinting analysis with deoxyribonuclease I was used to show that Sp1 binds to six GC box sequences within the c-Ha-ras1 promoter. An in vivo transfection assay showed competition between the 21-base pair repeats of the SV40 promoter and the c-Ha-ras1 promoter for common regulatory factors. In this system the presence of Sp1 is apparently required for c-Ha-ras1 transcription. Analysis of deletions of the c-Ha-ras1 promoter region by means of a transient expression assay revealed that the three Sp1 binding sites closest to the RNA start sites were sufficient for full transcriptional activity.
ras基因家族的成员编码的蛋白质,在过量产生或发生突变时能够使永生化的哺乳动物细胞发生转化。因此,了解ras基因的调控机制非常重要。人类哈维ras原癌基因c-Ha-ras1的启动子区域在多个位点起始RNA转录,并且包含六核苷酸GGGCGG及其反向互补序列CCGCCC的重复拷贝,即所谓的GC框。这些GC框由与SV40早期启动子中发现的序列相同的序列组成,人类细胞转录因子Sp1可结合于该启动子。利用脱氧核糖核酸酶I进行的足迹分析表明,Sp1可结合于c-Ha-ras1启动子内的六个GC框序列。一项体内转染试验显示,SV40启动子的21碱基对重复序列与c-Ha-ras1启动子之间存在对共同调控因子的竞争。在该系统中,c-Ha-ras1转录显然需要Sp1的存在。通过瞬时表达试验对c-Ha-ras1启动子区域缺失情况的分析表明,最靠近RNA起始位点的三个Sp1结合位点对于完全转录活性而言已足够。