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细胞周期蛋白依赖性激酶抑制剂 p20 控制生物钟细胞周期计时。

Cyclin-dependent kinase inhibitor p20 controls circadian cell-cycle timing.

机构信息

Centre for Cell and Molecular Dynamics, Department of Cell and Developmental Biology, University College London, London WC1E 6DE, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):6835-40. doi: 10.1073/pnas.1217912110. Epub 2013 Apr 8.

Abstract

Specific stages of the cell cycle are often restricted to particular times of day because of regulation by the circadian clock. In zebrafish, both mitosis (M phase) and DNA synthesis (S phase) are clock-controlled in cell lines and during embryo development. Despite the ubiquitousness of this phenomenon, relatively little is known about the underlying mechanism linking the clock to the cell cycle. In this study, we describe an evolutionarily conserved cell-cycle regulator, cyclin-dependent kinase inhibitor 1d (20 kDa protein, p20), which along with p21, is a strongly rhythmic gene and directly clock-controlled. Both p20 and p21 regulate the G1/S transition of the cell cycle. However, their expression patterns differ, with p20 predominant in developing brain and peak expression occurring 6 h earlier than p21. p20 expression is also p53-independent in contrast to p21 regulation. Such differences provide a unique mechanism whereby S phase is set to different times of day in a tissue-specific manner, depending on the balance of these two inhibitors.

摘要

细胞周期的特定阶段通常由于生物钟的调节而局限于一天中的特定时间。在斑马鱼中,有丝分裂(M 期)和 DNA 合成(S 期)在细胞系和胚胎发育过程中都受到生物钟的控制。尽管这种现象无处不在,但对于将生物钟与细胞周期联系起来的潜在机制,人们知之甚少。在这项研究中,我们描述了一种进化上保守的细胞周期调节剂,细胞周期蛋白依赖性激酶抑制剂 1d(20kDa 蛋白,p20),它与 p21 一起是一个节律性很强的基因,直接受生物钟控制。p20 和 p21 都调节细胞周期的 G1/S 期转变。然而,它们的表达模式不同,p20 在发育中的大脑中占优势,表达峰值比 p21 早 6 小时出现。与 p21 调节不同,p20 的表达不受 p53 的影响。这种差异提供了一种独特的机制,通过这种机制,根据这两种抑制剂的平衡,S 期以组织特异性的方式设置在一天中的不同时间。

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