Serchov Tsvetan, Jilg Antje, Wolf Christian T, Radtke Ina, Stehle Jörg H, Heumann Rolf
Department of Molecular Neurobiochemistry, Ruhr-University, 44780, Bochum, Germany.
International Graduate School of Neuroscience, Ruhr-University, 44780, Bochum, Germany.
Mol Neurobiol. 2016 Apr;53(3):1843-1855. doi: 10.1007/s12035-015-9135-0. Epub 2015 Mar 12.
Circadian rhythms, generated in the mouse suprachiasmatic nucleus (SCN), are synchronized to the environmental day-night changes by photic input. The activation of the extracellular signal-regulated kinases 1 and 2 (ERK1,2) and cAMP response element-binding protein (CREB)-mediated transcription play a critical role in this photoentrainment. The small GTPase Ras is one of the major upstream regulators of the ERK1,2/CREB pathway. In contrast to the well-described role of Ras in structural and functional synaptic plasticity in the adult mouse brain, the physiological regulation of Ras by photic sensory input is yet unknown. Here, we describe for the first time a circadian rhythm of Ras activity in the mouse SCN. Using synRas transgenic mice, expressing constitutively activated V12-Ha-Ras selectively in neurons, we demonstrate that enhanced Ras activation causes shortening of the circadian period length. We found upregulated expression and decreased inhibitory phosphorylation of the circadian period length modulator, glycogen synthase kinase-3 beta (GSK3β), in the SCN of synRas mice. Conversely, downregulation of Ras activity by blocking its function with an antibody in oscillating cell cultures reduced protein levels and increased phosphorylation of GSK3β and lengthened the period of BMAL1 promoter-driven luciferase activity. Furthermore, enhanced Ras activity in synRas mice resulted in a potentiation of light-induced phase delays at early subjective night, and increased photic induction of pERK1,2/pCREB and c-Fos. In contrast, at late subjective night, photic activation of Ras/ERK1,2/CREB in synRas mice was not sufficient to stimulate c-Fos protein expression and phase advance the clock. Taken together, our results demonstrate that Ras activity fine tunes the period length and modulates photoentrainment of the circadian clock.
在小鼠视交叉上核(SCN)中产生的昼夜节律通过光信号输入与环境中的昼夜变化同步。细胞外信号调节激酶1和2(ERK1,2)的激活以及cAMP反应元件结合蛋白(CREB)介导的转录在这种光诱导同步中起关键作用。小GTP酶Ras是ERK1,2/CREB途径的主要上游调节因子之一。与Ras在成年小鼠大脑结构和功能突触可塑性中所描述的作用不同,光感觉输入对Ras的生理调节尚不清楚。在这里,我们首次描述了小鼠SCN中Ras活性的昼夜节律。使用在神经元中选择性表达组成型激活的V12-Ha-Ras的synRas转基因小鼠,我们证明增强的Ras激活会导致昼夜周期长度缩短。我们发现synRas小鼠的SCN中昼夜周期长度调节因子糖原合酶激酶-3β(GSK3β)的表达上调且抑制性磷酸化降低。相反,在振荡细胞培养物中用抗体阻断Ras功能来下调其活性,会降低蛋白水平并增加GSK3β的磷酸化,延长BMAL1启动子驱动的荧光素酶活性的周期。此外,synRas小鼠中增强的Ras活性导致在主观夜早期光诱导的相位延迟增强,并增加了pERK1,2/pCREB和c-Fos的光诱导。相比之下,在主观夜后期,synRas小鼠中Ras/ERK1,2/CREB的光激活不足以刺激c-Fos蛋白表达并使生物钟提前。综上所述,我们的结果表明Ras活性微调周期长度并调节昼夜节律钟的光诱导同步。