Ruan Xiangbo, Li Ping, Cangelosi Andrew, Yang Ling, Cao Haiming
Center for Molecular Medicine, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892, USA.
Center for Molecular Medicine, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892, USA.
Cell Rep. 2016 Mar 1;14(8):1867-75. doi: 10.1016/j.celrep.2016.01.062. Epub 2016 Feb 18.
Glucose levels in mammals are tightly controlled through multiple mechanisms to meet systemic energy demands. Downregulation of hepatic glucokinase (GCK) during fasting facilitates the transition of the liver from a glucose-consuming to a gluconeogenic organ. Here, we report the transcriptional regulation of hepatic GCK by a long non-coding RNA (lncRNA) named liver GCK repressor (lncLGR). lncLGR is induced by fasting, and physiological overexpression of lncLGR to mimic fasting levels effectively suppresses GCK expression and reduces hepatic glycogen content in mice. Consistently, lncLGR knockdown enhances GCK expression and glycogen storage in fasted mice. Mechanistically, lncLGR specifically binds to heterogenous nuclear ribonucleoprotein L (hnRNPL), which is further confirmed to be a transcriptional repressor of GCK in vivo. Finally, we demonstrate that lncLGR facilitates the recruitment of hnRNPL to the GCK promoter and suppresses GCK transcription. Our data establish a lncRNA-mediated mechanism that regulates hepatic GCK expression and glycogen deposition in a physiological context.
哺乳动物的血糖水平通过多种机制受到严格控制,以满足全身能量需求。禁食期间肝葡萄糖激酶(GCK)的下调有助于肝脏从消耗葡萄糖的器官转变为糖异生器官。在此,我们报告了一种名为肝脏GCK抑制因子(lncLGR)的长链非编码RNA(lncRNA)对肝脏GCK的转录调控。lncLGR由禁食诱导,lncLGR的生理过表达以模拟禁食水平可有效抑制小鼠的GCK表达并降低肝脏糖原含量。同样,lncLGR敲低可增强禁食小鼠的GCK表达和糖原储存。从机制上讲,lncLGR特异性结合异质性核糖核蛋白L(hnRNPL),这在体内进一步证实是GCK的转录抑制因子。最后,我们证明lncLGR促进hnRNPL募集到GCK启动子并抑制GCK转录。我们的数据建立了一种lncRNA介导的机制,该机制在生理背景下调节肝脏GCK表达和糖原沉积。