Rencurel F, Waeber G, Antoine B, Rocchiccioli F, Maulard P, Girard J, Leturque A
Centre de Recherche sur l'Endocrinologie Moléculaire et le Développement, Meudon, France.
Biochem J. 1996 Mar 15;314 ( Pt 3)(Pt 3):903-9. doi: 10.1042/bj3140903.
Previous studies have shown that glucose increases the glucose transporter (GLUT2) mRNA expression in the liver in vivo and in vitro. Here we report an analysis of the effects of glucose metabolism on GLUT2 gene expression. GLUT2 mRNA accumulation by glucose was not due to stabilization of its transcript but rather was a direct effect on gene transcription. A proximal fragment of the 5' regulatory region of the mouse GLUT2 gene linked to a reporter gene was transiently transfected into liver GLUT2-expressing cells. Glucose stimulated reporter gene expression in these cells, suggesting that glucose-responsive elements were included within the proximal region of the promoter. A dose-dependent effect of glucose on GLUT2 expression was observed over 10 mM glucose irrespective of the hexokinase isozyme (glucokinase K(m) 16 mM; hexokinase I K(m) 0.01 mM) present in the cell type used. This suggests that the correlation between extracellular glucose and GLUT2 mRNA concentrations is simply a reflection of an activation of glucose metabolism. The mediators and the mechanism responsible for this response remain to be determined. In conclusion, glucose metabolism is required for the proper induction of the GLUT2 gene in the liver and this effect is transcriptionally regulated.
先前的研究表明,葡萄糖在体内和体外均可增加肝脏中葡萄糖转运蛋白(GLUT2)的mRNA表达。在此,我们报告了一项关于葡萄糖代谢对GLUT2基因表达影响的分析。葡萄糖引起的GLUT2 mRNA积累并非由于其转录本的稳定,而是对基因转录的直接影响。将与报告基因相连的小鼠GLUT2基因5'调控区的近端片段瞬时转染到表达肝脏GLUT2的细胞中。葡萄糖刺激了这些细胞中报告基因的表达,这表明葡萄糖反应元件包含在启动子的近端区域内。无论所用细胞类型中存在何种己糖激酶同工酶(葡萄糖激酶Km为16 mM;己糖激酶I Km为0.01 mM),在10 mM以上的葡萄糖浓度下均观察到葡萄糖对GLUT2表达的剂量依赖性效应。这表明细胞外葡萄糖与GLUT2 mRNA浓度之间的相关性仅仅是葡萄糖代谢激活的一种反映。负责这种反应的介质和机制仍有待确定。总之,肝脏中GLUT2基因的正常诱导需要葡萄糖代谢,并且这种效应是由转录调控的。