Jørgensen E C, Autrup H
Department of Environmental and Occupational Medicine, University of Aarhus, Denmark.
FEBS Lett. 1995 May 29;365(2-3):101-7. doi: 10.1016/0014-5793(95)00456-j.
The expression of the cytochrome P4501A1 gene, CYP1A1, is induced by e.g. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) mainly by transcriptional mechanisms. The inducers mediate their effect upon binding and activation of the aryl hydrocarbon receptor (AHR) transcription-factor complex. Utilizing chimeric CYP1A1/CAT constructs transient gene expression experiments indicate that the putative negative regulatory element (NRE) of CYP1A1 influence the relative TCDD induced CAT activity in HepG2 cells, whereas this effect was not observed in MCF-7 cells. Differences in the formation of cell-specific protein-DNA complexes were demonstrated by gel retardation assays suggesting a functional difference of NRE in these two cell lines.
细胞色素P4501A1基因(CYP1A1)的表达主要通过转录机制,例如被2,3,7,8 - 四氯二苯并 - p - 二恶英(TCDD)诱导。诱导剂通过与芳烃受体(AHR)转录因子复合物结合并激活来介导其作用。利用嵌合CYP1A1/CAT构建体进行的瞬时基因表达实验表明,CYP1A1的假定负调控元件(NRE)影响HepG2细胞中TCDD诱导的相对CAT活性,而在MCF - 7细胞中未观察到这种效应。凝胶阻滞分析证明了细胞特异性蛋白质 - DNA复合物形成的差异,表明NRE在这两种细胞系中存在功能差异。