The G0/G1 switch gene 2 is a novel PPAR target gene

Fokko Zandbergen, Stéphane Mandard, Pascal Escher, Nguan Soon Tan, David Patsouris, Tim Jatkoe, Sandra Rojas-Caro, Steve Madore, Walter Wahli, Sherrie Tafuri, Michael Müller, Sander Kersten*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

193 Citations (Scopus)

Abstract

PPARs (peroxisome-proliferator-activated receptors) α, β/δ and γ are a group of transcription factors that are involved in numerous processes, including lipid metabolism and adipogenesis. By comparing liver mRNAs of wild-type and PPARα-null mice using microarrays, a novel putative target gene of PPARα, G0S2 (G0/G1 switch gene 2), was identified. Hepatic expression of G0S2 was up-regulated by fasting and by the PPARα agonist Wy14643 in a PPARα-dependent manner. Surprisingly, the G0S2 mRNA level was highest in brown and white adipose tissue and was greatly up-regulated during mouse 3T3-L1 and human SGBS (Simpson-Golabi-Behmel syndrome) adipogenesis. Transactivation, gel shift and chromatin immunoprecipitation assays indicated that G0S2 is a direct PPARγ and probable PPARα target gene with a functional PPRE (PPAR-responsive element) in its promoter. Upregulation of G0S2 mRNA seemed to be specific for adipogenesis, and was not observed during osteogenesis or myogenesis. In 3T3-L1 fibroblasts, expression of G0S2 was associated with growth arrest, which is required for 3T3-L1 adipogenesis. Together, these data indicate that G0S2 is a novel target gene of PPARs that may be involved in adipocyte differentiation.

Original languageEnglish
Pages (from-to)313-324
Number of pages12
JournalBiochemical Journal
Volume392
Issue number2
DOIs
Publication statusPublished - Dec 1 2005
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Keywords

  • Adipogenesis
  • G/G switch gene 2 (G0S2)
  • Growth arrest
  • Peroxisome-proliferator-activated receptor (PPAR)

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