Zambon Alexander C, McDearmon Erin L, Salomonis Nathan, Vranizan Karen M, Johansen Kirsten L, Adey Deborah, Takahashi Joseph S, Schambelan Morris, Conklin Bruce R
Gladstone Institute of Cardiovascular Disease, Department of Medicine, University of California, San Francisco, CA 94141, USA.
Genome Biol. 2003;4(10):R61. doi: 10.1186/gb-2003-4-10-r61. Epub 2003 Sep 25.
Skeletal muscle remodeling is a critical component of an organism's response to environmental changes. Exercise causes structural changes in muscle and can induce phase shifts in circadian rhythms, fluctuations in physiology and behavior with a period of around 24 hours that are maintained by a core clock mechanism. Both exercise-induced remodeling and circadian rhythms rely on the transcriptional regulation of key genes.
We used DNA microarrays to determine the effects of resistance exercise (RE) on gene regulation in biopsy samples of human quadriceps muscle obtained 6 and 18 hours after an acute bout of isotonic exercise with one leg. We also profiled diurnal gene regulation at the same time points (2000 and 0800 hours) in the non-exercised leg. Comparison of our results with published circadian gene profiles in mice identified 44 putative genes that were regulated in a circadian fashion. We then used quantitative PCR to validate the circadian expression of selected gene orthologs in mouse skeletal muscle.
The coordinated regulation of the circadian clock genes Cry1, Per2, and Bmal1 6 hours after RE and diurnal genes 18 hours after RE in the exercised leg suggest that RE may directly modulate circadian rhythms in human skeletal muscle.
骨骼肌重塑是生物体对环境变化做出反应的关键组成部分。运动可导致肌肉结构变化,并能诱导昼夜节律的相位偏移,即生理和行为的波动,其周期约为24小时,由核心生物钟机制维持。运动诱导的重塑和昼夜节律均依赖于关键基因的转录调控。
我们使用DNA微阵列来确定抗阻运动(RE)对单腿进行急性等张运动6小时和18小时后获取的人股四头肌活检样本中基因调控的影响。我们还在同一时间点(2000和0800时)对未运动腿的昼夜基因调控进行了分析。将我们的结果与已发表的小鼠昼夜节律基因图谱进行比较,确定了44个以昼夜节律方式调控的假定基因。然后我们使用定量PCR来验证所选基因直系同源物在小鼠骨骼肌中的昼夜表达。
运动腿在RE后6小时生物钟基因Cry1、Per2和Bmal1以及RE后18小时昼夜基因的协同调控表明,RE可能直接调节人类骨骼肌的昼夜节律。