Li Z, Paulin D
Laboratoire de Biologie Moléculaire de la Différentiation Cellulaire, Université Paris 7, France.
J Biol Chem. 1993 May 15;268(14):10403-15.
We have previously reported that high level human desmin expression depends on a 280-base pair muscle-specific enhancer which can function not only in myotubes, but can also activate gene expression in myoblasts. We report here that this enhancer contains two different regions, one active in myotubes and the other in myoblasts. In the myotube-specific region, one MyoD1 site and one MEF2 site are necessary for full enhancer activity. Site-directed mutation of the MyoD1 binding site revealed that the intact site is essential for gene expression in myotubes and for transactivation by MyoD1 or myogenin in co-transfected fibroblasts. In the myoblast-specific region, four regions are protected by nuclear factors from the myogenic cell line C2, 7; three regions contain a GC-rich sequence sharing homology with the Krox binding site. Deletion and site-directed mutation experiments demonstrated that at least two Krox-like sequences are required for enhancer activity in myoblasts. In addition, another GC-rich sequence, designated Mb, is also required for full enhancer activity in myoblasts.
我们之前曾报道,高水平的人结蛋白表达依赖于一个280个碱基对的肌肉特异性增强子,该增强子不仅能在肌管中发挥作用,还能在成肌细胞中激活基因表达。我们在此报道,这个增强子包含两个不同区域,一个在肌管中活跃,另一个在成肌细胞中活跃。在肌管特异性区域,一个肌分化因子1(MyoD1)位点和一个肌细胞增强因子2(MEF2)位点对于增强子的完全活性是必需的。对MyoD1结合位点进行定点突变显示,完整的位点对于肌管中的基因表达以及共转染的成纤维细胞中MyoD1或生肌调节因子(myogenin)的反式激活至关重要。在成肌细胞特异性区域,来自成肌细胞系C2、7的核因子保护四个区域;三个区域含有与Krox结合位点具有同源性的富含GC的序列。缺失和定点突变实验表明,成肌细胞中增强子活性至少需要两个类似Krox的序列。此外,另一个富含GC的序列,命名为Mb,对于成肌细胞中增强子的完全活性也是必需的。