Department of Diabetes and Endocrinology, Saitama Medical University, Saitama 350-0495, Japan.
J Atheroscler Thromb. 2010 Feb;17(1):73-83. doi: 10.5551/jat.2410. Epub 2010 Jan 21.
PPARgamma (peroxisome proliferator-activated receptor gamma) is a member of the nuclear receptor superfamily of ligand-activated transcription factors that regulate the expression of genes associated with lipid metabolism. Herein, we show that expression levels of the novel PPARgamma transcript exhibit circadian oscillation. To study the mechanisms controlling PPARgamma expression, a novel PPARgamma gene promoter was cloned and characterized.
We analyzed the novel PPARgamma promoter by luciferase reporter assays and gel shift analysis.
Surprisingly, it was not an intron but rather the novel first exon of PPARgamma that was found to have functional minimal promoter activity. Luciferase reporter assays and gel shift assays revealed that the novel first exon is essential for novel PPARgamma promoter activation and that DBP (albumin gene D-site binding protein) and E4BP4 (E4 promoter A binding protein 4) bind directly to D-sites in the novel first exon.
Our results demonstrate that the PAR-bZIP (bZIP, basic leucine zipper) family and E4BP4 are the main regulatory factors involved in oscillation of novel PPARgamma expression. This regulatory mechanism clearly differs from that of the circadian expression of PPARalpha.
过氧化物酶体增殖物激活受体γ(PPARγ)是核受体超家族配体激活转录因子的成员,调节与脂质代谢相关基因的表达。在此,我们发现新型 PPARγ 转录本的表达水平呈现昼夜节律性波动。为了研究控制 PPARγ 表达的机制,我们克隆并鉴定了一个新型 PPARγ 基因启动子。
我们通过荧光素酶报告基因检测和凝胶迁移分析来分析新型 PPARγ 启动子。
令人惊讶的是,具有功能的最小启动子活性的是新型 PPARγ 的第一个外显子,而不是内含子。荧光素酶报告基因检测和凝胶迁移分析表明,新型第一外显子对于新型 PPARγ 启动子的激活至关重要,并且 DBP(白蛋白基因 D 位点结合蛋白)和 E4BP4(E4 启动子 A 结合蛋白 4)直接与新型第一外显子中的 D 位点结合。
我们的结果表明,PAR-bZIP(bZIP,碱性亮氨酸拉链)家族和 E4BP4 是参与新型 PPARγ 表达昼夜节律波动的主要调节因子。这种调节机制明显不同于 PPARα 的昼夜表达。