Thinakaran G, Ojala J, Bag J
Department of Molecular Biology and Genetics, University of Guelph, Ont., Canada.
FEBS Lett. 1993 Mar 22;319(3):271-6. doi: 10.1016/0014-5793(93)80561-8.
Mitogen withdrawal triggers myogenic differentiation in skeletal myoblasts in culture. We have examined the expression of the proto-oncogene c-jun during this process in mouse C2C12 myoblasts. c-jun belongs to a family of immediate early genes whose expression is activated in cultured cells in response to the addition of serum growth factors. Interestingly, expression of c-jun was maintained in mouse C2C12 and rat L6 myoblasts undergoing myogenic differentiation under low-serum conditions. Previously it has been reported that expression of c-jun is downregulated during differentiation of C2 cells. However, our results using C2C12 cells, a subclone of the C2 line, show that c-jun mRNA, protein and the activator-protein 1 (AP-1) DNA-binding activity were easily detected in proliferating myoblasts and differentiated myotubes. Although overexpression of c-jun has been shown to block myogenic differentiation in C2 cells, results presented here suggest that expression of c-jun at physiological levels may not interfere with skeletal myogenesis.
有丝分裂原撤除会引发培养的骨骼肌成肌细胞的肌源性分化。我们研究了原癌基因c-jun在小鼠C2C12成肌细胞这一过程中的表达情况。c-jun属于即刻早期基因家族,其表达在培养细胞中会因添加血清生长因子而被激活。有趣的是,在低血清条件下经历肌源性分化的小鼠C2C12和大鼠L6成肌细胞中,c-jun的表达得以维持。此前有报道称,在C2细胞分化过程中c-jun的表达会下调。然而,我们使用C2系的一个亚克隆C2C12细胞所得到的结果表明,在增殖的成肌细胞和分化的肌管中很容易检测到c-jun mRNA、蛋白质以及激活蛋白1(AP-1)的DNA结合活性。尽管已表明c-jun的过表达会阻断C2细胞的肌源性分化,但此处给出的结果表明,生理水平的c-jun表达可能不会干扰骨骼肌生成。