Hall R K, Sladek F M, Granner D K
Department of Molecular Physiology and Biophysics, Vanderbilt University Medical School, Nashville, TN 37232-0615.
Proc Natl Acad Sci U S A. 1995 Jan 17;92(2):412-6. doi: 10.1073/pnas.92.2.412.
Glucocorticoids stimulate hepatic phosphoenolpyruvate carboxykinase (PEPCK; EC 4.1.1.32) gene expression, thereby increasing the rate of gluconeogenesis. The effect of glucocorticoids on PEPCK gene expression is mediated by a set of promoter elements collectively referred to as the glucocorticoid response unit. The response unit spans a 100-bp segment and includes two glucocorticoid receptor binding sites (GR1 and GR2) and two accessory factor binding sites (AF1 and AF2), all of which are required for a maximal glucocorticoid response. The AF1 element also serves as a retinoic acid response element and may be involved in developmental and tissue-specific expression of the gene. In this study we report that COUP-TF and HNF-4, two orphan members of the nuclear receptor superfamily, bind to the AF1 element and function as accessory factors for the glucocorticoid response of the PEPCK gene.
糖皮质激素刺激肝磷酸烯醇式丙酮酸羧激酶(PEPCK;EC 4.1.1.32)基因表达,从而提高糖异生速率。糖皮质激素对PEPCK基因表达的作用是由一组统称为糖皮质激素反应单元的启动子元件介导的。该反应单元跨越一个100bp的片段,包括两个糖皮质激素受体结合位点(GR1和GR2)和两个辅助因子结合位点(AF1和AF2),所有这些对于最大糖皮质激素反应都是必需的。AF1元件还作为视黄酸反应元件,可能参与该基因的发育和组织特异性表达。在本研究中,我们报告了核受体超家族的两个孤儿成员COUP-TF和HNF-4与AF1元件结合,并作为PEPCK基因糖皮质激素反应的辅助因子发挥作用。