Jiangsu Key Laboratory for Molecular and Medical Biotechnology and College of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.
Hepatology. 2011 Oct;54(4):1410-20. doi: 10.1002/hep.24514. Epub 2011 Aug 19.
Many aspects of energy metabolism, including glucose and lipid homeostasis and mitochondrial oxidative metabolism, are under precise control by the mammalian circadian clock. However, the molecular mechanism for coordinate integration of the circadian clock and various metabolic pathways is poorly understood. Here we show that BAF60a, a chromatin-remodeling complex subunit, is rhythmically expressed in the liver of mice. Mice with liver-specific knockdown of BAF60a show abnormalities in the rhythmic expression pattern of clock and metabolic genes and in the circulating metabolite profile. Consistently, knockdown of BAF60a impairs the oscillation of clock genes in serum-shocked HepG(2) cells. At the molecular level, BAF60a activates Bmal1 and G6Pase transcription by way of the coactivation of retinoid-related orphan receptor alpha (RORα). In addition, BAF60a is present near ROR response elements (RORE) on the proximal Bmal1 and G6Pase promoters and turns the chromatin structure into the active state.
Our data suggest a critical role for BAF60a in the coordinated regulation of hepatic circadian clock and energy metabolism in mammals.
许多能量代谢方面,包括葡萄糖和脂质稳态和线粒体氧化代谢,都受到哺乳动物生物钟的精确控制。然而,生物钟和各种代谢途径的协调整合的分子机制还了解甚少。在这里,我们表明,BAF60a,染色质重塑复合物亚基,在小鼠肝脏中呈节律性表达。肝特异性 BAF60a 敲低的小鼠表现出时钟和代谢基因的节律表达模式以及循环代谢物谱的异常。一致地,BAF60a 敲低会损害血清冲击 HepG(2)细胞中时钟基因的振荡。在分子水平上,BAF60a 通过激活视黄酸相关孤儿受体 α(RORα)来激活 Bmal1 和 G6Pase 的转录。此外,BAF60a 存在于近端 Bmal1 和 G6Pase 启动子上的 ROR 反应元件(RORE)附近,并将染色质结构转变为活性状态。
我们的数据表明 BAF60a 在哺乳动物肝脏生物钟和能量代谢的协调调节中起着关键作用。