Yamamoto Yoshinobu, Yagita Kazuhiro, Okamura Hitoshi
Division of Molecular Brain Science, Department of Brain Sciences, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
Mol Cell Biol. 2005 Mar;25(5):1912-21. doi: 10.1128/MCB.25.5.1912-1921.2005.
To explore the role of mPer2 in the circadian oscillation in the mammalian cellular clock, we established fibroblast cell lines in which expression of mPer2 is controlled through a tetracycline-regulatable promoter. We revealed that constitutive expression and overexpression of mPer2 mRNA severely impair serum shock-induced cyclic circadian clock gene expression. Moreover, under conditions of lower mPer2 mRNA expression, mPER2 protein accumulation in these cells showed clear circadian oscillation even in constitutive mPer2 mRNA expression, suggesting that the protein cycling of mPER2 was required for oscillation of the circadian feedback loop. Since the rhythms of gene expression driven by the intrinsic clock oscillation system dampen rapidly in the absence of cyclic expression of mPer2, the transcriptional rhythm helps to sustain the clock oscillation.
为了探究mPer2在哺乳动物细胞生物钟昼夜节律振荡中的作用,我们建立了成纤维细胞系,其中mPer2的表达通过四环素调控启动子进行控制。我们发现,mPer2 mRNA的组成型表达和过表达严重损害血清休克诱导的昼夜节律时钟基因的周期性表达。此外,在较低mPer2 mRNA表达的条件下,即使在mPer2 mRNA组成型表达的情况下,这些细胞中mPER2蛋白的积累也表现出明显的昼夜节律振荡,这表明mPER2的蛋白循环是昼夜反馈环振荡所必需的。由于在缺乏mPer2周期性表达的情况下,由内在生物钟振荡系统驱动的基因表达节律会迅速衰减,因此转录节律有助于维持生物钟振荡。