Liu Xiao, Dang Yunkun, Matsu-Ura Toru, He Yubo, He Qun, Hong Christian I, Liu Yi
Department of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9040, USA.
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, OH 45267, USA.
Mol Cell. 2017 Jul 20;67(2):203-213.e4. doi: 10.1016/j.molcel.2017.05.029. Epub 2017 Jun 22.
Although the coupling between circadian and cell cycles allows circadian clocks to gate cell division and DNA replication in many organisms, circadian clocks were thought to function independently of cell cycle. Here, we show that DNA replication is required for circadian clock function in Neurospora. Genetic and pharmacological inhibition of DNA replication abolished both overt and molecular rhythmicities by repressing frequency (frq) gene transcription. DNA replication is essential for the rhythmic changes of nucleosome composition at the frq promoter. The FACT complex, known to be involved in histone disassembly/reassembly, is required for clock function and is recruited to the frq promoter in a replication-dependent manner to promote replacement of histone H2A.Z by H2A. Finally, deletion of H2A.Z uncoupled the dependence of the circadian clock on DNA replication. Together, these results establish circadian clock and cell cycle as interdependent coupled oscillators and identify DNA replication as a critical process in the circadian mechanism.
尽管昼夜节律与细胞周期之间的耦合使得昼夜节律钟能够在许多生物体中控制细胞分裂和DNA复制,但昼夜节律钟曾被认为独立于细胞周期发挥作用。在此,我们表明DNA复制对于脉孢菌中的昼夜节律钟功能是必需的。DNA复制的遗传和药理学抑制通过抑制频率(frq)基因转录消除了明显的和分子节律性。DNA复制对于frq启动子处核小体组成的节律性变化至关重要。已知参与组蛋白拆卸/重新组装的FACT复合物对于生物钟功能是必需的,并以复制依赖的方式被招募到frq启动子上,以促进H2A取代组蛋白H2A.Z。最后,H2A.Z的缺失解除了昼夜节律钟对DNA复制的依赖性。总之,这些结果将昼夜节律钟和细胞周期确立为相互依赖的耦合振荡器,并将DNA复制确定为昼夜节律机制中的一个关键过程。