E3 ubiquitin ligase E6AP negatively regulates adipogenesis by downregulating proadipogenic factor C/EBPalpha

PLoS One. 2013 Jun 7;8(6):e65330. doi: 10.1371/journal.pone.0065330. Print 2013.

Abstract

CCAAT/Enhancer Binding Protein Alpha (C/EBPα) is a key transcription factor involved in the adipocyte differentiation. Here for the first time we demonstrate that E6AP, an E3 ubiquitin ligase inhibits adipocyte differentiation in 3T3-L1 cells as revealed by reduced lipid staining with oil red. Knock down of E6AP in mouse 3T3L1 preadipocytes is sufficient to convert them to adipocytes independent of external hormonal induction. C/EBPα protein level is drastically increased in E6AP deficient 3T3L1 preadipocytes while inverse is observed when wild type E6AP is over expressed. We show that transient transfection of wild type E6AP downregulates C/EBPα protein expression in a dose dependent manner while catalytically inactive E6AP-C843A rather stabilizes it. In addition, wild type E6AP inhibits expression of proadipogenic genes while E6AP-C843A enhances them. More importantly, overexpression of E6AP-C843A in mesenchymal progenitor cells promotes accumulation of lipid droplets while there is drastically reduced lipid droplet formation when E6AP is over expressed. Taken together, our finding suggests that E6AP may negatively control adipogenesis by inhibiting C/EBPα expression by targeting it to ubiquitin-proteasome pathway for degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / metabolism
  • Adipogenesis*
  • Animals
  • Biocatalysis
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • CCAAT-Enhancer-Binding Protein-alpha / genetics
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism*
  • Cell Differentiation
  • Cell Separation
  • Down-Regulation*
  • Gene Knockdown Techniques
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Models, Biological
  • Mutant Proteins / metabolism
  • RNA, Small Interfering / metabolism
  • Transcriptional Activation / genetics
  • Ubiquitin-Protein Ligases / metabolism*
  • Up-Regulation

Substances

  • CCAAT-Enhancer-Binding Protein-alpha
  • Mutant Proteins
  • RNA, Small Interfering
  • Ube3a protein, mouse
  • Ubiquitin-Protein Ligases

Grants and funding

The authors are sincerely thankful to CSIR-Central Drug Research Institute for its financial support in the completion of this project. This work was supported by CSIR grants HCP0004, BSC0201i and DBT grant GAP00068 to AKT, and ICMR Senior research fellowship to P Pal. Institutional (CSIR-CDRI), Institutional manuscript number for this article is 49/2012/AKT. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.