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 language | English |
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Pages (from-to) | 313-324 |
Number of pages | 12 |
Journal | Biochemical Journal |
Volume | 392 |
Issue number | 2 |
DOIs | |
Publication status | Published - Dec 1 2005 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Molecular Biology
- Cell Biology
Keywords
- Adipogenesis
- G/G switch gene 2 (G0S2)
- Growth arrest
- Peroxisome-proliferator-activated receptor (PPAR)