Joshi Radhika, Cai Yao D, Xia Yongliang, Chiu Joanna C, Emery Patrick
Department of Neurobiology, University of Massachusetts Chan Medical School, Worcester, MA, United States.
Department of Entomology and Nematology, University of California, Davis, Davis, CA, United States.
Front Physiol. 2022 Jun 2;13:888262. doi: 10.3389/fphys.2022.888262. eCollection 2022.
Ambient temperature varies constantly. However, the period of circadian pacemakers is remarkably stable over a wide-range of ecologically- and physiologically-relevant temperatures, even though the kinetics of most biochemical reactions accelerates as temperature rises. This thermal buffering phenomenon, called temperature compensation, is a critical feature of circadian rhythms, but how it is achieved remains elusive. Here, we uncovered the important role played by the PERIOD (PER) phosphodegron in temperature compensation. This phosphorylation hotspot is crucial for PER proteasomal degradation and is the functional homolog of mammalian PER2 S478 phosphodegron, which also impacts temperature compensation. Using CRISPR-Cas9, we introduced a series of mutations that altered three Serines of the PER phosphodegron. While all three Serine to Alanine substitutions lengthened period at all temperatures tested, temperature compensation was differentially affected. S44A and S45A substitutions caused undercompensation, while S47A resulted in overcompensation. These results thus reveal unexpected functional heterogeneity of phosphodegron residues in thermal compensation. Furthermore, mutations impairing phosphorylation of the phosphocluster showed undercompensation, consistent with its inhibitory role on S47 phosphorylation. We observed that S47A substitution caused increased accumulation of hyper-phosphorylated PER at warmer temperatures. This finding was corroborated by cell culture assays in which S47A slowed down phosphorylation-dependent PER degradation at high temperatures, causing PER degradation to be excessively temperature-compensated. Thus, our results point to a novel role of the PER phosphodegron in temperature compensation through temperature-dependent modulation of the abundance of hyper-phosphorylated PER. Our work reveals interesting mechanistic convergences and differences between mammalian and temperature compensation of the circadian clock.
环境温度不断变化。然而,尽管大多数生化反应的动力学随着温度升高而加快,但昼夜节律起搏器的周期在广泛的生态和生理相关温度范围内却非常稳定。这种热缓冲现象,称为温度补偿,是昼夜节律的一个关键特征,但其实现方式仍然难以捉摸。在这里,我们发现了周期蛋白(PER)磷酸化降解结构域在温度补偿中发挥的重要作用。这个磷酸化热点对于PER蛋白酶体降解至关重要,并且是哺乳动物PER2 S478磷酸化降解结构域的功能同源物,后者也影响温度补偿。我们使用CRISPR-Cas9技术引入了一系列突变,这些突变改变了PER磷酸化降解结构域的三个丝氨酸。虽然所有三个丝氨酸到丙氨酸的替换都在所有测试温度下延长了周期,但温度补偿受到了不同的影响。S44A和S45A替换导致补偿不足,而S47A则导致补偿过度。因此,这些结果揭示了磷酸化降解结构域残基在热补偿中意想不到的功能异质性。此外,损害磷酸簇磷酸化的突变表现出补偿不足,这与其对S47磷酸化的抑制作用一致。我们观察到S47A替换在较高温度下导致过度磷酸化的PER积累增加。这一发现得到了细胞培养实验的证实,在该实验中,S47A在高温下减缓了磷酸化依赖性PER的降解,导致PER降解过度温度补偿。因此,我们的结果指出了PER磷酸化降解结构域在温度补偿中的一个新作用,即通过温度依赖性调节过度磷酸化PER的丰度来实现。我们的工作揭示了哺乳动物和昼夜节律时钟温度补偿之间有趣的机制趋同和差异。