Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Methods Mol Biol. 2021;2130:195-203. doi: 10.1007/978-1-0716-0381-9_15.
Daily rhythms of behaviors and physiologies are driven by transcriptional-translational negative feedback loops of clock genes and encoded clock proteins (Bass and Takahashi Science 330:1349-1354, 2010; Brown et al. Dev Cell 22:477-487, 2012). Posttranslational modifications of clock proteins, including protein phosphorylation, play an essential role for normal oscillation of the circadian clock through regulation of their activities, stabilities, interactions, and intracellular localization (Gallego and Virshup Nat Rev Mol Cell Biol 8:139-148, 2007; Hirano et al. Nat Struct Mol Biol 23:1053-1060, 2016). In this chapter, we describe detailed methods for quantitative analysis of phosphorylation levels of clock proteins, particularly focusing on circadian phosphorylation of CLOCK, BMAL1, and their complex (Yoshitane et al. Mol Cell Biol 29:3675-3686, 2009).
昼夜节律的行为和生理学是由时钟基因和编码时钟蛋白的转录-翻译负反馈环驱动的(Bass 和 Takahashi Science 330:1349-1354, 2010; Brown 等人 Dev Cell 22:477-487, 2012)。时钟蛋白的翻译后修饰,包括蛋白磷酸化,通过调节其活性、稳定性、相互作用和细胞内定位,对生物钟的正常振荡起着至关重要的作用(Gallego 和 Virshup Nat Rev Mol Cell Biol 8:139-148, 2007; Hirano 等人 Nat Struct Mol Biol 23:1053-1060, 2016)。在本章中,我们描述了定量分析时钟蛋白磷酸化水平的详细方法,特别是聚焦于 CLOCK、BMAL1 及其复合物的昼夜磷酸化(Yoshitane 等人 Mol Cell Biol 29:3675-3686, 2009)。