A novel long noncoding RNA Lnc-HC binds hnRNPA2B1 to regulate expressions of Cyp7a1 and Abca1 in hepatocytic cholesterol metabolism

  • Xi Lan
  • , Jidong Yan
  • , Juan Ren
  • , Bo Zhong
  • , Jing Li
  • , Yue Li
  • , Li Liu
  • , Jing Yi
  • , Qingzhu Sun
  • , Xudong Yang
  • , Jian Sun
  • , Liesu Meng
  • , Wenhua Zhu
  • , Rikard Holmdahl
  • , Dongmin Li
  • , Shemin Lu

Research output: Contribution to journalArticlepeer-review

121 Scopus citations

Abstract

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. Conclusion: 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).

Original languageEnglish
Pages (from-to)58-72
Number of pages15
JournalHepatology
Volume64
Issue number1
DOIs
StatePublished - 1 Jul 2016

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