| Literature DB >> 12734185 |
Naoya Yahagi1, Hitoshi Shimano, Takashi Matsuzaka, Yuho Najima, Motohiro Sekiya, Yoshimi Nakagawa, Tomohiro Ide, Sachiko Tomita, Hiroaki Okazaki, Yoshiaki Tamura, Yoko Iizuka, Ken Ohashi, Takanari Gotoda, Ryozo Nagai, Satoshi Kimura, Shun Ishibashi, Jun-Ichi Osuga, Nobuhiro Yamada.
Abstract
The tumor suppressor p53 is a transcription factor that activates or represses its target genes after various genotoxic stresses. We have previously shown that sterol regulatory element-binding protein-1 (SREBP-1), a key transcriptional regulator of triglyceride synthesis, and the lipogenic enzymes under its control are markedly suppressed in adipocytes from genetically obese ob/ob mice. Here we demonstrate that p53 and its target genes are highly induced in adipocytes of ob/ob mice in a fed state, leading to the negative regulation of SREBP-1 and thereby lipogenic genes. In fact, disruption of p53 in ob/ob mice completely suppressed the p53-regulated genes to wild-type levels and partially restored expression of lipogenic enzymes. Consistently, reporter gene analysis showed that p53 overexpression suppressed the promoter activity of the SREBP-1c gene and its downstream genes. Thus, the activation of p53 might constitute a negative feedback loop against excess fat accumulation in adipocytes. In conclusion, we discovered a novel role of p53 in the pathophysiology of obesity.Entities:
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Year: 2003 PMID: 12734185 DOI: 10.1074/jbc.M302364200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157