甾醇调节元件结合蛋白
脂质代谢
脂肪酸合酶
生物
乙酰辅酶A羧化酶
生物化学
脂肪酸合成
新陈代谢
甘油三酯
脂肪酸代谢
脂肪生成
转基因
脂肪酸
基因表达
基因
丙酮酸羧化酶
胆固醇
酶
作者
Li Duan,Min Cheng,Yuqiang Niu,Xiaojing Chi,Xiuying Liu,Jingjing Fan,Heng Fan,Yongsheng Chang,Wei Yang
摘要
Sterol regulatory element binding proteins (SREBPs) are master regulators of hepatic lipid homeostasis. Aberrant expression of SREBPs frequently leads to lipid metabolism dysregulation. Long non-coding RNAs (lncRNAs) have been identified with diverse biological functions, but the effects of lncRNAs on lipid metabolism are rarely reported. Here, we identified a novel human specific lncRNA, lncHR1, as a negative regulator of SREBP-1c expression. Overexpression of lncHR1 inhibited expression of SREBP-1c and fatty acid synthase (FAS) and then repressed oleic acid-induced hepatic cell triglyceride (TG) and lipid droplet (LD) accumulation. In vivo, the data of established transgenic animals showed that mice with lncHR1 expression had less hepatic expression of SREBP-1c, FAS, Acetyl-CoA carboxylase α (ACCα), and less hepatic and plasma TG after being fed a high-fat diet. Therefore, we report a novel lncRNA which can decrease lipid metabolism by repressing SREBP-1c gene expression.
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