Banting and Best Department of Medical Research, University of Toronto, Toronto, Ontario, Canada.
J Steroid Biochem Mol Biol. 1992 Dec;43(8):937-50. doi: 10.1016/0960-0760(92)90322-A.
Cyp-21 (the mouse steroid 21-hydroxylase gene) is expressed exclusively in cells of the adrenal cortex, is induced by ACTH and cAMP, and is required for corticosteroid synthesis. This review examines the molecular basis for the regulated expression of Cyp-21 in the ACTH-responsive, mouse adrenocortical tumor cell line, Y1. We demonstrate that 330 bp of 5'-flanking DNA from the Cyp-21 gene are sufficient for cell-selective and ACTH-induced expression of Cyp-21, and that this promoter region comprises multiple, closely spaced enhancer elements each of which is required for promoter function. Within this promoter, we define three related elements that contain variations of an AGGTCA motif and that contribute to the cell-selective expression of Cyp-21. Variations of these same AGGTCA-bearing elements are also involved in the expression of Cyp 11a and Cyp 11b in Y1 adrenocortical cells. These elements interact with the same or closely related nuclear proteins found only in steroidogenic cell lines. Taken together, these results suggest that shared elements contribute to the adrenal cell-selective expression of at least three steroidogenic cytochrome P450 genes. The element at -170 and the related elements at -65, -140 and -210 in the Cyp-21 promoter are not active as enhancers in the mutant Y1 cell line, Kin-8. Kin-8 cells contain a mutation in the regulatory subunit of the type 1 cAMP-dependent protein kinase that renders the enzyme resistant to activation by cAMP. Therefore, these elements appear to be selectively dependent upon an intact cAMP-dependent protein kinase for enhancer function. Individually, none of these elements confer cAMP-dependence to a reporter gene driven by a heterologous promoter. On the basis of these observations, we suggest that ACTH- and cAMP-dependent expression of Cyp-21 requires the combined actions of the element at -170, and the related elements at -140, -210 and -65.
Cyp-21(鼠甾体 21-羟化酶基因)仅在肾上腺皮质细胞中表达,受 ACTH 和 cAMP 诱导,是皮质类固醇合成所必需的。本综述探讨了 Cyp-21 在 ACTH 反应性、鼠肾上腺皮质肿瘤细胞系 Y1 中受调控表达的分子基础。我们证明,Cyp-21 基因 5'侧翼 DNA 的 330bp 足以实现细胞选择性和 ACTH 诱导的 Cyp-21 表达,并且该启动子区域包含多个紧密间隔的增强子元件,每个元件都需要启动子功能。在这个启动子内,我们定义了三个相关的元件,它们包含 AGGTCA 基序的变体,有助于 Cyp-21 的细胞选择性表达。这些相同的 AGGTCA 带元件的变体也参与了 Y1 肾上腺皮质细胞中 Cyp11a 和 Cyp11b 的表达。这些元件与仅在甾体生成细胞系中发现的相同或密切相关的核蛋白相互作用。总之,这些结果表明,共享元件有助于至少三种甾体生成细胞色素 P450 基因的肾上腺细胞选择性表达。Cyp-21 启动子中的-170 元件和相关的-65、-140 和-210 元件在突变的 Y1 细胞系 Kin-8 中不作为增强子发挥作用。Kin-8 细胞包含 1 型 cAMP 依赖性蛋白激酶的调节亚基的突变,使该酶对 cAMP 的激活产生抗性。因此,这些元件似乎选择性地依赖于完整的 cAMP 依赖性蛋白激酶来发挥增强子功能。单独地,这些元件中的任何一个都不会赋予由异源启动子驱动的报告基因对 cAMP 的依赖性。基于这些观察结果,我们认为 Cyp-21 的 ACTH 和 cAMP 依赖性表达需要-170 元件和相关的-140、-210 和-65 元件的共同作用。