Imai E, Miner J N, Mitchell J A, Yamamoto K R, Granner D K
Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee 37232-0615.
J Biol Chem. 1993 Mar 15;268(8):5353-6.
The phosphoenolpyruvate carboxykinase (PEPCK) gene encodes the rate-limiting enzyme in gluconeogenesis. Glucocorticoids enhance PEPCK gene expression through a multicomponent regulatory complex. We show that a full response to glucocorticoids requires two DNA segments: 1) a glucocorticoid response unit (GRU), centered at about position -400, which contains two accessory factor elements (AF1 and AF2) and two glucocorticoid receptor binding sites (GR1 and GR2), and 2) a basal promoter/cyclic AMP response element (E/CRE) at about position -90, which binds the transcription factor CREB. A protein-protein interaction was observed in vitro between GR and CREB that might account for the role of the E/CRE in the glucocorticoid response of the PEPCK gene.
磷酸烯醇式丙酮酸羧激酶(PEPCK)基因编码糖异生过程中的限速酶。糖皮质激素通过一个多组分调节复合体增强PEPCK基因的表达。我们发现,对糖皮质激素的充分应答需要两个DNA片段:1)一个糖皮质激素反应单元(GRU),位于约-400位置处,它包含两个辅助因子元件(AF1和AF2)以及两个糖皮质激素受体结合位点(GR1和GR2);2)一个位于约-90位置处的基础启动子/环磷酸腺苷反应元件(E/CRE),它结合转录因子CREB。在体外观察到GR和CREB之间存在蛋白质-蛋白质相互作用,这可能解释了E/CRE在PEPCK基因糖皮质激素应答中的作用。