Gekakis N, Staknis D, Nguyen H B, Davis F C, Wilsbacher L D, King D P, Takahashi J S, Weitz C J
Department of Neurobiology, Harvard Medical School, Boston MA 02115, USA. 02115, USA.
Science. 1998 Jun 5;280(5369):1564-9. doi: 10.1126/science.280.5369.1564.
The mouse Clock gene encodes a bHLH-PAS protein that regulates circadian rhythms and is related to transcription factors that act as heterodimers. Potential partners of CLOCK were isolated in a two-hybrid screen, and one, BMAL1, was coexpressed with CLOCK and PER1 at known circadian clock sites in brain and retina. CLOCK-BMAL1 heterodimers activated transcription from E-box elements, a type of transcription factor-binding site, found adjacent to the mouse per1 gene and from an identical E-box known to be important for per gene expression in Drosophila. Mutant CLOCK from the dominant-negative Clock allele and BMAL1 formed heterodimers that bound DNA but failed to activate transcription. Thus, CLOCK-BMAL1 heterodimers appear to drive the positive component of per transcriptional oscillations, which are thought to underlie circadian rhythmicity.
小鼠生物钟基因编码一种bHLH-PAS蛋白,该蛋白调节昼夜节律,并且与作为异源二聚体起作用的转录因子相关。通过双杂交筛选分离出了生物钟(CLOCK)的潜在伙伴,其中一个伙伴BMAL1,与生物钟(CLOCK)及周期蛋白1(PER1)在大脑和视网膜中已知的昼夜节律位点共表达。生物钟(CLOCK)-BMAL1异源二聚体激活了E-盒元件的转录,E-盒元件是一种转录因子结合位点,位于小鼠周期蛋白1(per1)基因附近,并且也存在于一个对果蝇周期蛋白(per)基因表达很重要的相同E-盒中。来自显性负性生物钟(Clock)等位基因的突变型生物钟(CLOCK)和BMAL1形成了结合DNA但无法激活转录的异源二聚体。因此,生物钟(CLOCK)-BMAL1异源二聚体似乎驱动了周期蛋白(per)转录振荡的正向成分,而这种振荡被认为是昼夜节律的基础。