Skapek S X, Rhee J, Spicer D B, Lassar A B
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Science. 1995 Feb 17;267(5200):1022-4. doi: 10.1126/science.7863328.
Although the myogenic regulator MyoD is expressed in proliferating myoblasts, differentiation of these cells is limited to the G0 phase of the cell cycle. Forced expression of cyclin D1, but not cyclins A, B, or E, inhibited the ability of MyoD to transactivate muscle-specific genes and correlated with phosphorylation of MyoD. Transfection of myoblasts with cyclin-dependent kinase (Cdk) inhibitors p21 and p16 augmented muscle-specific gene expression in cells maintained in high concentrations of serum, suggesting that an active cyclin-Cdk complex suppresses MyoD function in proliferating cells.
尽管生肌调节因子MyoD在增殖的成肌细胞中表达,但这些细胞的分化仅限于细胞周期的G0期。细胞周期蛋白D1的强制表达而非细胞周期蛋白A、B或E的强制表达,抑制了MyoD反式激活肌肉特异性基因的能力,并与MyoD的磷酸化相关。用细胞周期蛋白依赖性激酶(Cdk)抑制剂p21和p16转染成肌细胞,可增强在高浓度血清中培养的细胞的肌肉特异性基因表达,这表明活性细胞周期蛋白-Cdk复合物在增殖细胞中抑制MyoD功能。