Heidelberg University, Biochemistry Center, Im Neuenheimer Feld 328, D-69120 Heidelberg, Germany.
Division Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.
Nat Commun. 2016 Jun 24;7:11807. doi: 10.1038/ncomms11807.
The circadian clock and the cell cycle are major cellular systems that organize global physiology in temporal fashion. It seems conceivable that the potentially conflicting programs are coordinated. We show here that overexpression of MYC in U2OS cells attenuates the clock and conversely promotes cell proliferation while downregulation of MYC strengthens the clock and reduces proliferation. Inhibition of the circadian clock is crucially dependent on the formation of repressive complexes of MYC with MIZ1 and subsequent downregulation of the core clock genes BMAL1 (ARNTL), CLOCK and NPAS2. We show furthermore that BMAL1 expression levels correlate inversely with MYC levels in 102 human lymphomas. Our data suggest that MYC acts as a master coordinator that inversely modulates the impact of cell cycle and circadian clock on gene expression.
生物钟和细胞周期是组织细胞全局生理学的主要系统。似乎可以想象,潜在的冲突程序是协调的。我们在这里表明,在 U2OS 细胞中过表达 MYC 会减弱生物钟,相反,促进细胞增殖,而下调 MYC 会增强生物钟并减少增殖。生物钟的抑制严重依赖于 MYC 与 MIZ1 形成抑制性复合物,随后下调核心生物钟基因 BMAL1(ARNTL)、CLOCK 和 NPAS2。我们还表明,在 102 个人类淋巴瘤中,BMAL1 表达水平与 MYC 水平呈负相关。我们的数据表明,MYC 作为一个主协调因子,反向调节细胞周期和生物钟对基因表达的影响。