Xiang S, Parsons H K, Murray M
Storr Liver Unit, Department of Medicine, University of Sydney, Westmead Hospital, Westmead, NSW 2145, Australia.
Gene. 1998 Mar 16;209(1-2):123-9. doi: 10.1016/s0378-1119(98)00017-1.
A novel regulatory element (27 bp) which confers transcriptional repression was identified within the protein-coding region immediately after the translation start codon in the human cytochrome P450 (CYP) 2C9 gene. Deletion of this element increased transcriptional activity in HepG2 cells by transient transfection assay. Nuclear protein extracts from HepG2 cells and human liver were found in electrophoretic mobility shift assays to bind specifically to the 27 bp element. A putative binding protein was partially purified by DNA-affinity chromatography and was determined by Southwestern blotting to have a molecular weight of approx. 100 kDa. Studies with mutated competitor oligonucleotides established that binding of the nuclear protein to the 27 bp cis-element was dependent upon two 6 bp direct repeats (5'-CTTGTG-3') that were separated by three bases. It is possible that this novel cis-acting element may be involved in the negative regulation of CYP2C9.
在人细胞色素P450(CYP)2C9基因翻译起始密码子后的蛋白质编码区内,鉴定出一种新型调控元件(27bp),其具有转录抑制作用。通过瞬时转染实验,该元件的缺失增加了HepG2细胞中的转录活性。在电泳迁移率变动分析中发现,来自HepG2细胞和人肝脏的核蛋白提取物能与27bp元件特异性结合。通过DNA亲和层析对一种假定的结合蛋白进行了部分纯化,并通过蛋白质印迹法确定其分子量约为100kDa。对突变竞争寡核苷酸的研究表明,核蛋白与27bp顺式元件的结合依赖于由三个碱基分隔的两个6bp直接重复序列(5'-CTTGTG-3')。这种新型顺式作用元件可能参与了CYP2C9的负调控。