Fujii-Kuriyama Y, Imataka H, Sogawa K, Yasumoto K, Kikuchi Y
Department of Chemistry, Faculty of Science, Tohoku University, Sendai, Japan.
FASEB J. 1992 Jan 6;6(2):706-10. doi: 10.1096/fasebj.6.2.1537460.
CYP1A1 is considered to be involved mainly in oxidative metabolism of exogenous chemicals and drugs. Synthesis of this hemoprotein is induced in livers, lungs, and other tissues of experimental animals by the administration of these chemicals. Regulatory mechanisms of the induction process of the protein have been investigated by the DNA transfer method using the isolated genomic DNA. At least two kinds of cis-acting regulatory DNA sequences are localized 5' upstream of the gene. One is distributed five times in a relatively wide range from -0.5 to -3.5 kb and functions as an inducible enhancer-designated xenobiotic responsive element or XRE. The other is localized just upstream of the TATA sequence and acts as a regulatory element for the constitutive expression. The two DNA elements are required for a high level of the inducible expression. Their cognate DNA binding factors are recognized in the nuclear extracts of Hepa-1 cells and rat liver cells which show the inducible expression of CYP1A1 in response to the inducer. This paper discusses the regulatory mechanisms of CYP1A1 gene expression by summarizing the present state of knowledge about properties of the DNA regulatory elements and their cognate DNA-binding factors.
细胞色素P450 1A1(CYP1A1)主要参与外源性化学物质和药物的氧化代谢。通过给予这些化学物质,可在实验动物的肝脏、肺及其他组织中诱导这种血红蛋白的合成。利用分离的基因组DNA通过DNA转移方法研究了该蛋白诱导过程的调控机制。至少有两种顺式作用调控DNA序列位于该基因5'上游。一种在从-0.5至-3.5 kb的相对较宽范围内分布五次,起诱导增强子的作用,称为外源性物质反应元件(XRE)。另一种位于TATA序列的正上游,作为组成型表达的调控元件。这两个DNA元件对于高水平的诱导表达是必需的。在对诱导剂有反应而表现出CYP1A1诱导表达的Hepa-1细胞和大鼠肝细胞的核提取物中识别出它们的同源DNA结合因子。本文通过总结关于DNA调控元件及其同源DNA结合因子特性的现有知识,讨论了CYP1A1基因表达的调控机制。