CHRONO regulates the circadian clock via the REV-ERBα - BMAL1 loop.

Qin Zhou, Lanxin Gao, Ruohan Wang, Shaoying Lan, Dan Li, Ximing Qin
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Abstract

The period length of the circadian clock is important for organisms to maintain homeostasis. CHRONO has been shown to play an important role in regulating the period of the mammalian clock and has recently been implicated to function in several important physiological aspects. However, the mechanisms underlying transcriptional regulation by CHRONO to determine the circadian period remain elusive. Here, we report that CHRONO acts as a transcriptional repressor on JUN/FOS complexes independent of the classical BMAL1/CLOCK complexes. CHRONO can regulate BMAL1 expression by differentially regulating REV-ERBα and REV-ERBβ. We further developed a mathematical model and the model simulations strongly agreed with our findings that CHRONO acts on both REV-ERBα and BMAL1 to regulate the circadian period. The model also sheds light on the physiological significance of the fact that CHRONO cycles in most of the mammalian tissues. Thus, our experimental and computational approaches reveal the molecular mechanisms of regulating the circadian period by an important circadian component, CHRONO.

CHRONO通过rev - erba - BMAL1回路调节生物钟。
生物钟的周期长度对生物体维持体内平衡很重要。CHRONO已被证明在调节哺乳动物生物钟周期中发挥重要作用,最近被认为在几个重要的生理方面发挥作用。然而,CHRONO决定昼夜节律的转录调控机制仍然难以捉摸。在这里,我们报道了CHRONO作为JUN/FOS复合物的转录抑制因子独立于经典的BMAL1/CLOCK复合物。CHRONO可通过差异调节rev - erba和rev - erbb β来调节BMAL1的表达。我们进一步建立了一个数学模型,模型模拟结果与我们的发现非常一致,即CHRONO同时作用于rev - erba和BMAL1来调节昼夜节律。该模型还揭示了CHRONO在大多数哺乳动物组织中循环的生理意义。因此,我们的实验和计算方法揭示了通过重要的昼夜节律成分CHRONO调节昼夜节律周期的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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