Santalucía T, Moreno H, Palacín M, Yacoub M H, Brand N J, Zorzano A
Department of Cardiothoracic Surgery, National Heart and Lung Institute, Faculty of Medicine, Imperial College of Science, Technology and Medicine, London, SW3 6LY, UK.
J Mol Biol. 2001 Nov 23;314(2):195-204. doi: 10.1006/jmbi.2001.5091.
We report tripartite co-operation between MyoD, myocyte enhancer factor-2 (MEF2) and the thyroid hormone receptor (TRalpha1) that takes place in the context of an 82-bp muscle-specific enhancer in the rat insulin-responsive glucose transporter (GLUT4) gene that is active in both cardiac and skeletal muscle. In the L6E9 skeletal muscle cell line and in 10T1/2 fibroblasts, a powerful synergistic activation of the GLUT4 enhancer relied on the over-expression of MyoD, MEF2 and TRalpha1 and the integrity of their respective binding sites, and occurred when linked to either a heterologous promoter or in the context of the native GLUT4 promoter. In cardiac myocytes, enhancer activity was dependent on the binding sites for MEF2 and TRalpha1. Furthermore, we show that in 10T1/2 fibroblasts, the forced expression of MyoD, MEF2 and TRalpha1 induced the expression of the endogenous, otherwise silent, GLUT4 gene. In all, our results indicate a novel functional co-operation between these three factors which is required for full activation of GLUT4 transcription.
我们报道了肌分化因子(MyoD)、肌细胞增强因子2(MEF2)和甲状腺激素受体(TRα1)之间的三方合作,这种合作发生在大鼠胰岛素反应性葡萄糖转运蛋白(GLUT4)基因中一个82碱基对的肌肉特异性增强子的背景下,该增强子在心肌和骨骼肌中均有活性。在L6E9骨骼肌细胞系和10T1/2成纤维细胞中,GLUT4增强子的强大协同激活依赖于MyoD、MEF2和TRα1的过表达及其各自结合位点的完整性,并且当与异源启动子相连或在天然GLUT4启动子的背景下均会发生。在心肌细胞中,增强子活性依赖于MEF2和TRα1的结合位点。此外,我们表明在10T1/2成纤维细胞中,MyoD、MEF2和TRα1的强制表达诱导了内源性、原本沉默的GLUT4基因的表达。总之,我们的结果表明这三种因子之间存在一种新的功能合作,这是GLUT4转录完全激活所必需的。