Department of Neurobiology, Harvard Medical School, Boston, MA 02115.
Proc Natl Acad Sci U S A. 2013 Oct 1;110(40):16021-6. doi: 10.1073/pnas.1305980110. Epub 2013 Sep 16.
Circadian clocks in mammals are built on a negative feedback loop in which the heterodimeric transcription factor circadian locomotor output cycles kaput (CLOCK)-brain, muscle Arnt-like 1 (BMAL1) drives the expression of its own inhibitors, the PERIOD and CRYPTOCHROME proteins. Reactivation of CLOCK-BMAL1 occurs at a specific time several hours after PERIOD and CRYPTOCHROME protein turnover, but the mechanism underlying this process is unknown. We found that mouse BMAL1 complexes include TRAP150 (thyroid hormone receptor-associated protein-150; also known as THRAP3). TRAP150 is a selective coactivator for CLOCK-BMAL1, which oscillates under CLOCK-BMAL1 transcriptional control. TRAP150 promotes CLOCK-BMAL1 binding to target genes and links CLOCK-BMAL1 to the transcriptional machinery at target-gene promoters. Depletion of TRAP150 caused low-amplitude, long-period rhythms, identifying it as a positive clock element. The activity of TRAP150 defines a positive feedback loop within the clock and provides a potential mechanism for timing the reactivation of circadian transcription.
哺乳动物的生物钟是建立在一个负反馈环上的,其中异二聚体转录因子生物钟输出周期蛋白(CLOCK)-脑,肌肉 ARNT 样蛋白 1(BMAL1)驱动其自身抑制剂 PERIOD 和 CRYPTOCHROME 蛋白的表达。PERIOD 和 CRYPTOCHROME 蛋白周转数小时后,CLOCK-BMAL1 会重新激活,但该过程的机制尚不清楚。我们发现,小鼠 BMAL1 复合物包括 TRAP150(甲状腺激素受体相关蛋白 150;也称为 THRAP3)。TRAP150 是 CLOCK-BMAL1 的选择性共激活因子,在 CLOCK-BMAL1 转录控制下振荡。TRAP150 促进 CLOCK-BMAL1 与靶基因结合,并将 CLOCK-BMAL1 与靶基因启动子上的转录机制联系起来。TRAP150 的耗竭导致振幅低、周期长的节律,将其鉴定为正向时钟元件。TRAP150 的活性在时钟内定义了一个正反馈环,并为生物钟重新激活提供了一个潜在的机制。