Regulatory Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Chronobiology Unit, Groningen Institute for Evolutionary Life Sciences, University of Groningen, 9700 CC Groningen, the Netherlands.
Cell Rep. 2024 Mar 26;43(3):113951. doi: 10.1016/j.celrep.2024.113951. Epub 2024 Mar 19.
Plasticity in daily timing of activity has been observed in many species, yet the underlying mechanisms driving nocturnality and diurnality are unknown. By regulating how much wheel-running activity will be rewarded with a food pellet, we can manipulate energy balance and switch mice to be nocturnal or diurnal. Here, we present the rhythmic transcriptome of 21 tissues, including 17 brain regions, sampled every 4 h over a 24-h period from nocturnal and diurnal male CBA/CaJ mice. Rhythmic gene expression across tissues comprised different sets of genes with minimal overlap between nocturnal and diurnal mice. We show that non-clock genes in the suprachiasmatic nucleus (SCN) change, and the habenula was most affected. Our results indicate that adaptive flexibility in daily timing of behavior is supported by gene expression dynamics in many tissues and brain regions, especially in the habenula, which suggests a crucial role for the observed nocturnal-diurnal switch.
在许多物种中都观察到了日常活动时间的可塑性,但驱动夜行性和昼行性的潜在机制尚不清楚。通过调节轮跑活动将获得多少食物颗粒作为奖励,我们可以操纵能量平衡并将老鼠转变为夜行性或昼行性。在这里,我们展示了来自夜行性和昼行性雄性 CBA/CaJ 小鼠的 21 种组织(包括 17 个脑区)的每 4 小时采样一次的 24 小时周期的节律转录组。跨组织的节律基因表达由不同的基因组成,夜行性和昼行性小鼠之间的重叠最小。我们表明,视交叉上核(SCN)中的非生物钟基因发生变化,而缰核受影响最大。我们的研究结果表明,行为日常时间的适应性灵活性是由许多组织和脑区的基因表达动态支持的,特别是在缰核中,这表明观察到的昼夜转换起着关键作用。