Du Rong, An Xiao-Rong, Chen Yong-Fu, Qin Jian
State Key Laboratory for Agrobiotechnology, College of Biological Science, China Agricultural University, Beijing, 100094, P.R. China.
J Biochem Mol Biol. 2007 Jul 31;40(4):547-53. doi: 10.5483/bmbrep.2007.40.4.547.
Many motifs along the 1.2 kb myostatin promoter (MSTNpro) in sheep have been found by the MatInspecter program in our recent study. To further verify the role of the motifs and better understand the transcriptional regulation mechanism of the myostatin gene in sheep, the reporter gene EGFP (enhanced green fluorescent protein) was selected and the wild-type (W) vector MSTNPro(W)-EGFP or motif-mutational (M) vector MSTNPro(M)-EGFP were constructed. The transcriptional regulation activities were analyzed by detecting the fluorescence strength of EGFP in C2C12 myoblasts transfected with the vectors. The results showed that E-box (E) 3, E4, E5 and E7, particularly E3, E5 and E7, had important effects on the activity of the 1.2 kb sheep myostatin promoter. In addition, we also detected several other important motifs such as MTBF (muscle-specific Mt binding factor), MEF2 (myocyte enhancer factor 2), GRE (glucocorticoid response elements) and PRE (progesterone response elements) along the sheep myostatin promoter by the mutational analysis.
在我们最近的研究中,通过MatInspecter程序在绵羊1.2 kb肌肉生长抑制素启动子(MSTNpro)上发现了许多基序。为了进一步验证这些基序的作用,并更好地理解绵羊肌肉生长抑制素基因的转录调控机制,选择了报告基因EGFP(增强型绿色荧光蛋白),构建了野生型(W)载体MSTNPro(W)-EGFP或基序突变型(M)载体MSTNPro(M)-EGFP。通过检测用这些载体转染的C2C12成肌细胞中EGFP的荧光强度来分析转录调控活性。结果表明,E-box(E)3、E4、E5和E7,尤其是E3、E5和E7,对1.2 kb绵羊肌肉生长抑制素启动子的活性有重要影响。此外,我们还通过突变分析检测了绵羊肌肉生长抑制素启动子上的其他几个重要基序,如MTBF(肌肉特异性Mt结合因子)、MEF2(肌细胞增强因子2)、GRE(糖皮质激素反应元件)和PRE(孕酮反应元件)。