Department of Health Sciences, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, Anhui, China.
Int J Mol Sci. 2020 Apr 2;21(7):2469. doi: 10.3390/ijms21072469.
Circadian rhythm is an endogenous, self-sustainable oscillation that participates in regulating organisms' physiological activities. Key to this oscillation is a negative feedback by the main clock components Periods and Cryptochromes that repress the transcriptional activity of BMAL1/CLOCK (defined in the Abbreviations) complexes. In addition, a novel repressor, CHRONO, has been identified recently, but details of CHRONO's function during repressing the circadian cycle remain unclear. Here we report that a domain of CHRONO mainly composed of α-helixes is critical to repression through the exploitation of protein-protein interactions according to luciferase reporter assays, co-immunoprecipitation, immunofluorescence, genome editing, and structural information analysis via circular dichroism spectroscopy. This repression is fulfilled by interactions between CHRONO and a region on the C-terminus of BMAL1 where Cryptochrome and CBP (defined in the Abbreviations) bind. Our resultsindicate that CHRONO and PER differentially function as BMAL1/CLOCK-dependent repressors. Besides, the N-terminus of CHRONO is important for its nuclear localization. We further develop a repression model of how PER, CRY, and CHRONO proteins associate with BMAL1, respectively.
昼夜节律是一种内源性的、自我维持的振荡,参与调节生物体的生理活动。这种振荡的关键是主要时钟成分 Periods 和 Cryptochromes 通过抑制 BMAL1/CLOCK(在缩写中定义)复合物的转录活性来进行负反馈。此外,最近已经鉴定出一种新型的抑制剂 CHRONO,但 CHRONO 在抑制昼夜节律周期中的功能细节仍不清楚。在这里,我们报告说,CHRONO 的一个主要由α螺旋组成的结构域通过利用蛋白质-蛋白质相互作用来进行抑制,这是至关重要的,根据荧光素酶报告基因检测、共免疫沉淀、免疫荧光、基因组编辑和通过圆二色性光谱分析的结构信息分析。这种抑制是通过 CHRONO 与 BMAL1 的 C 末端上的一个区域之间的相互作用来实现的,Cryptochrome 和 CBP(在缩写中定义)结合在该区域上。我们的结果表明,CHRONO 和 PER 作为 BMAL1/CLOCK 依赖性抑制剂的功能不同。此外,CHRONO 的 N 端对于其核定位很重要。我们进一步开发了一个抑制模型,说明 PER、CRY 和 CHRONO 蛋白分别与 BMAL1 相关联。