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骨骼肌终末细胞周期停滞与MyoD诱导p21之间的相关性。

Correlation of terminal cell cycle arrest of skeletal muscle with induction of p21 by MyoD.

作者信息

Halevy O, Novitch B G, Spicer D B, Skapek S X, Rhee J, Hannon G J, Beach D, Lassar A B

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

出版信息

Science. 1995 Feb 17;267(5200):1018-21. doi: 10.1126/science.7863327.

Abstract

Skeletal muscle differentiation entails the coordination of muscle-specific gene expression and terminal withdrawal from the cell cycle. This cell cycle arrest in the G0 phase requires the retinoblastoma tumor suppressor protein (Rb). The function of Rb is negatively regulated by cyclin-dependent kinases (Cdks), which are controlled by Cdk inhibitors. Expression of MyoD, a skeletal muscle-specific transcriptional regulator, activated the expression of the Cdk inhibitor p21 during differentiation of murine myocytes and in nonmyogenic cells. MyoD-mediated induction of p21 did not require the tumor suppressor protein p53 and correlated with cell cycle withdrawal. Thus, MyoD may induce terminal cell cycle arrest during skeletal muscle differentiation by increasing the expression of p21.

摘要

骨骼肌分化需要协调肌肉特异性基因表达以及从细胞周期中终末退出。这种在G0期的细胞周期停滞需要视网膜母细胞瘤肿瘤抑制蛋白(Rb)。Rb的功能受到细胞周期蛋白依赖性激酶(Cdks)的负调控,而Cdks由细胞周期蛋白依赖性激酶抑制剂控制。MyoD是一种骨骼肌特异性转录调节因子,在小鼠肌细胞分化过程中和非肌细胞中,其表达激活了细胞周期蛋白依赖性激酶抑制剂p21的表达。MyoD介导的p21诱导不需要肿瘤抑制蛋白p53,且与细胞周期退出相关。因此,MyoD可能通过增加p21的表达来诱导骨骼肌分化过程中的终末细胞周期停滞。

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