Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University, Ministry of Education of China, Beijing, China.
Hepatology. 2016 Jul;64(1):58-72. doi: 10.1002/hep.28391. Epub 2016 Jan 22.
Cholesterol metabolism disorder in hepatocytes predicts a higher risk of metabolic syndrome (MetS). Long noncoding RNAs (lncRNAs) have emerged as critical players in cellular cholesterol metabolism, but their functions are not systematically clarified. Here, we have identified a novel lncRNA named lnc-HC negatively regulating cholesterol metabolism within hepatocytes through physical interaction with hnRNPA2B1. By further binding to the target messenger RNA of Cyp7a1 or Abca1, the lnc-HC-hnRNPA2B1 complex decreases expressions of the two genes that are implicated in cellular cholesterol excretion. lnc-HC knockdown can strongly recover the cholesterol disorder in vivo. In the upstream pathway, lnc-HC is up-regulated by high cholesterol by the transcription activator, CCAAT/enhancer-binding protein beta.
These findings suggest a subtle feed-forward regulation of lnc-HC in cholesterol metabolism and define a novel line of evidence by which lncRNAs modulate the metabolic system at the post-transcriptional level. (Hepatology 2016;64:58-72).
肝细胞中的胆固醇代谢紊乱预示着代谢综合征(MetS)的风险更高。长链非编码 RNA(lncRNA)已成为细胞胆固醇代谢的关键调控因子,但它们的功能尚未得到系统阐明。本研究中,我们发现了一种新的 lncRNA,命名为 lnc-HC,它通过与 hnRNPA2B1 的物理相互作用,在肝细胞内负调控胆固醇代谢。lnc-HC 进一步与 Cyp7a1 或 Abca1 的靶信使 RNA 结合,降低了两个与细胞胆固醇排泄相关基因的表达。lnc-HC 敲低可在体内强烈恢复胆固醇紊乱。在转录激活因子 CCAAT/增强子结合蛋白 β的作用下,lnc-HC 可被高胆固醇上调。
这些发现提示胆固醇代谢中 lnc-HC 的微妙正反馈调节,并为 lncRNA 在转录后水平调节代谢系统提供了新的证据。(《肝脏病学》2016;64:58-72)。