Yin Yang 1 promotes hepatic steatosis through repression of farnesoid X receptor in obese mice

Gut. 2014 Jan;63(1):170-8. doi: 10.1136/gutjnl-2012-303150. Epub 2013 Jan 24.

Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) is characterised by accumulation of excessive triglycerides in the liver. Obesity is usually associated with NAFLD through an unknown mechanism.

Objective: To investigate the roles of Yin Yang 1 (YY1) in the progression of obesity-associated hepatosteatosis.

Methods: Expression levels of hepatic YY1 were identified by microarray analysis in high-fat-diet (HFD)-induced obese mice. Liver triglyceride metabolism was analysed in mice with YY1 overexpression and suppression.

Results: YY1 expression was markedly upregulated in HFD-induced obese mice and NAFLD patients. Overexpression of YY1 in healthy mice promoted hepatosteatosis under high-fat dietary conditions, whereas liver-specific ablation of YY1 using adenoviral shRNA ameliorated triglyceride accumulation in obese mice. At the molecular level, YY1 suppressed farnesoid X receptor (FXR) expression through binding to the YY1 responsive element at intron 1 of the FXR gene.

Conclusions: These findings indicate that YY1 plays a crucial role in obesity-associated hepatosteatosis, through repression of FXR expression.

Keywords: Nonalcoholic Steatohepatitis; Signal Transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Blotting, Western
  • Chromatin Immunoprecipitation
  • Fatty Liver / etiology*
  • Fatty Liver / metabolism
  • Humans
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Non-alcoholic Fatty Liver Disease
  • Obesity / complications
  • Obesity / metabolism*
  • Oligonucleotide Array Sequence Analysis
  • Real-Time Polymerase Chain Reaction
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Triglycerides / metabolism
  • Up-Regulation
  • YY1 Transcription Factor / metabolism*

Substances

  • Biomarkers
  • Receptors, Cytoplasmic and Nuclear
  • Triglycerides
  • YY1 Transcription Factor
  • YY1 protein, human
  • Yy1 protein, mouse
  • farnesoid X-activated receptor