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Transcription factor AP-2β: A negative regulator of IRS-1 gene expression

2010; Elsevier BV; Volume: 392; Issue: 4 Linguagem: Inglês

10.1016/j.bbrc.2010.01.056

1090-2104

Xiangning Meng, Motoyuki Kondo, Katsutaro Morino, Tomoya Fuke, Toshiyuki Obata, Takeshi Yoshizaki, Satoshi Ugi, Yoshihiko Nishio, Shiro Maeda, Eiichi Araki, Atsunori Kashiwagi, Hiroshi Maegawa,

Metabolism, Diabetes, and Cancer

Down-regulation of insulin receptor substrate-1 (IRS-1) expression could modify the ability of IRS-1 to fulfill its functions. It has been proposed that the phosphorylation of IRS-1 on serine residues could promote its degradation. However, few studies have investigated the transcriptional regulation of IRS-1 in the pathogenesis of insulin resistance. Genotyping for genome-wide single nucleotide polymorphisms revealed that the transcription factor activating enhancer-binding protein-2β (AP-2β) is a novel candidate gene for conferring susceptibility to obesity and type 2 diabetes. AP-2β is expressed in adipose tissue and its expression is increased during the maturation of adipocytes. Overexpression of AP-2β leads to adipocyte hypertrophy, directly inhibits adiponectin expression, and enhanced the expression of inflammatory adipokines such as IL-6 and MCP-1. In this study, we found that overexpression of AP-2β in 3T3-L1 adipocytes impaired the promoter activity of IRS-1, and subsequently decreased mRNA and protein expression. Electrophoretic mobility shift assays showed that AP-2β bound specifically to the IRS-1 promoter region. Furthermore, site-directed mutagenesis of the AP-2 binding site located at −362 to −351, relative to the transcription start site, markedly decreased AP-2-induced suppression of IRS-1 promoter activity, whereas other putative AP-2 binding sites did not. Our results clearly showed that AP-2β directly decreased IRS-1 expression by binding to its promoter. Based on these findings, we speculate that the AP-2β transcriptional factor is a unique regulator of IRS-1 and a candidate gene for insulin resistance.