Chakir Ibtissam, Dumont Stéphanie, Pévet Paul, Ouarour Ali, Challet Etienne, Vuillez Patrick
Faculty of Science, Laboratory of Biology and Health, Abdelmalek Essaâdi University, BP2121, Tetouan 93002, Morocco; Regulation of Circadian Clocks Team, Institute for Cellular and Integrative Neurosciences, UPR3212, CNRS and University of Strasbourg, Strasbourg, France.
Regulation of Circadian Clocks Team, Institute for Cellular and Integrative Neurosciences, UPR3212, CNRS and University of Strasbourg, Strasbourg, France.
Brain Res. 2015 Jan 12;1594:165-72. doi: 10.1016/j.brainres.2014.10.063. Epub 2014 Nov 6.
A major challenge in the field of circadian rhythms is to understand the neural mechanisms controlling the oppositely phased temporal organization of physiology and behaviour between night- and day-active animals. Most identified components of the master clock in the suprachiasmatic nuclei (SCN), called circadian genes, display similar oscillations according to the time of day, independent of the temporal niche. This has led to the predominant view that the switch between night- and day-active animals occurs downstream of the master clock, likely also involving differential feedback of behavioral cues onto the SCN. The Barbary striped grass mouse, Lemniscomys barbarus is known as a day-active Muridae. Here we show that this rodent, when housed in constant darkness, displays a temporal rhythmicity of metabolism matching its diurnal behaviour (i.e., high levels of plasma leptin and hepatic glycogen during subjective midday and dusk, respectively). Regarding clockwork in their SCN, these mice show peaks in the mRNA profiles of the circadian gene Period1 (Per1) and the clock-controlled gene Vasopressin (Avp), which occur during the middle and late subjective day, respectively, in accordance with many observations in both diurnal and nocturnal species. Strikingly, expression of the circadian gene Clock in the SCN of the Barbary striped grass mouse was not constitutive as in nocturnal rodents, but it was rhythmic. As this is also the case for the other diurnal species investigated in the literature (sheep, marmoset, and quail), a hypothesis is that the transcriptional control of Clock within the SCN participates in the mechanisms underlying diurnality and nocturnality.
昼夜节律领域的一个主要挑战是理解控制夜行性动物和昼行性动物生理与行为相反相位时间组织的神经机制。视交叉上核(SCN)中大多数已确定的主时钟成分,即所谓的昼夜节律基因,会根据一天中的时间显示出相似的振荡,与时间生态位无关。这导致了一种主流观点,即夜行性动物和昼行性动物之间的转换发生在主时钟的下游,可能还涉及行为线索对SCN的差异反馈。北非条纹草鼠(Lemniscomys barbarus)是一种已知的昼行性鼠科动物。在这里我们表明,这种啮齿动物在持续黑暗环境中饲养时,其新陈代谢呈现出与昼夜行为相匹配的时间节律性(即分别在主观中午和黄昏时血浆瘦素和肝糖原水平较高)。关于它们SCN中的生物钟机制,这些小鼠在昼夜节律基因Period1(Per1)和生物钟控制基因加压素(Avp)的mRNA谱中出现峰值,分别出现在主观白天的中期和后期,这与在昼行性和夜行性物种中的许多观察结果一致。令人惊讶的是,北非条纹草鼠SCN中昼夜节律基因Clock的表达并不像夜行性啮齿动物那样是组成型的,而是有节律的。由于文献中研究的其他昼行性物种(绵羊、狨猴和鹌鹑)也是如此,因此有一种假设是,SCN内Clock的转录控制参与了昼夜性和夜行性的潜在机制。