Yang Yulin, Duan Zeyu, Liu Xiao-Lan, Li Zhanbiao, Shen Zhenghao, Gong Shimin, Lu Qiaojia, Hu Yue, Song Linhao, Wang Zeyu, Cao Xuemei, Dang Yunkun, Wang Linqi, He Qun, Liu Xiao
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
College of Life Sciences, University of the Chinese Academy of Sciences, Beijing 100049, China.
Nucleic Acids Res. 2025 Feb 27;53(5). doi: 10.1093/nar/gkaf162.
The interplay between circadian clocks, the cell cycle, and DNA repair has been extensively documented, yet the epigenetic control of circadian clocks by DNA damage responses remains relatively unexplored. Here, we showed that checkpoint kinases CHK1/2 regulate chromatin structure during DNA damage in Neurospora crassa to maintain robust circadian rhythms. Under DNA damage stress, deletion of chk1/2 disrupted the rhythmic transcription of the clock gene frq by suppressing the rhythmic binding of the transcription activator White Collar complex (WCC) at the frq promoter, as the chromatin structure remained condensed. Mechanistically, CHK1/2 interacted with WC-2 and were recruited by WCC to bind at the frq promoter to phosphorylate H3T11, promoting H3 acetylation, especially H3K56 acetylation, to counteract the histone variant H2A.Z deposition, thereby establishing a suitable chromatin state to maintain robust circadian rhythms despite DNA damage. Additionally, a genome-wide correlation was discovered between H3T11 phosphorylation and H3K56 acetylation, showing a specific function at the frq promoter that is dependent on CHK1/2. Furthermore, transcriptome analysis revealed that CHK1/2 are responsible for robust rhythmic transcription of metabolic and DNA repair genes during DNA damage. These findings highlight the essential role of checkpoint kinases in maintaining robust circadian rhythms under DNA damage stress.
昼夜节律时钟、细胞周期和DNA修复之间的相互作用已有大量文献记载,但DNA损伤反应对昼夜节律时钟的表观遗传控制仍相对未被探索。在此,我们表明,在粗糙脉孢菌中,检查点激酶CHK1/2在DNA损伤期间调节染色质结构,以维持稳健的昼夜节律。在DNA损伤应激下,chk1/2的缺失通过抑制转录激活因子白领复合物(WCC)在frq启动子处的节律性结合,破坏了时钟基因frq的节律性转录,因为染色质结构仍然浓缩。机制上,CHK1/2与WC-2相互作用,并被WCC招募到frq启动子处结合,使H3T11磷酸化,促进H3乙酰化,尤其是H3K56乙酰化,以抵消组蛋白变体H2A.Z的沉积,从而建立一个合适的染色质状态,尽管存在DNA损伤仍能维持稳健的昼夜节律。此外,还发现了H3T11磷酸化与H3K56乙酰化之间的全基因组相关性,表明在frq启动子处有一个依赖于CHK1/2的特定功能。此外,转录组分析表明,CHK1/2负责在DNA损伤期间代谢和DNA修复基因的稳健节律性转录。这些发现突出了检查点激酶在DNA损伤应激下维持稳健昼夜节律中的重要作用。