Vernon Ann E, Philpott Anna
Department of Oncology, University of Cambridge, Cambridge Institute for Medical Research, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2XY, UK.
Development. 2003 Jan;130(1):71-83. doi: 10.1242/dev.00180.
The molecular basis of the antagonism between cellular proliferation and differentiation is poorly understood. We have investigated the role of the cyclin-dependent kinase inhibitor p27(Xic1) in the co-ordination of cell cycle exit and differentiation during early myogenesis in vivo using Xenopus embryos. In this report, we demonstrate that p27(Xic1) is highly expressed in the developing myotome, that ablation of p27(Xic1) protein prevents muscle differentiation and that p27(Xic1) synergizes with the transcription factor MyoD to promote muscle differentiation. Furthermore, the ability of p27(Xic1) to promote myogenesis resides in an N-terminal domain and is separable from its cell cycle regulation function. This data demonstrates that a single cyclin-dependent kinase inhibitor, p27(Xic1), controls in vivo muscle differentiation in Xenopus and that regulation of this process by p27(Xic1) requires activities beyond cell cycle inhibition.
细胞增殖与分化之间拮抗作用的分子基础目前仍知之甚少。我们利用非洲爪蟾胚胎研究了细胞周期蛋白依赖性激酶抑制剂p27(Xic1)在体内早期肌生成过程中细胞周期退出与分化协调中的作用。在本报告中,我们证明p27(Xic1)在发育中的肌节中高表达,p27(Xic1)蛋白的缺失会阻止肌肉分化,并且p27(Xic1)与转录因子MyoD协同促进肌肉分化。此外,p27(Xic1)促进肌生成的能力存在于其N端结构域,并且与其细胞周期调节功能是可分离的。这些数据表明,单一的细胞周期蛋白依赖性激酶抑制剂p27(Xic1)在非洲爪蟾体内控制肌肉分化,并且p27(Xic1)对这一过程的调节需要超越细胞周期抑制的活性。