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孤儿核激素受体Rev-erbalpha调节人类载脂蛋白CIII启动子。

Orphan nuclear hormone receptor Rev-erbalpha regulates the human apolipoprotein CIII promoter.

作者信息

Coste Hervé, Rodríguez Joan C

机构信息

GlaxoSmithKline, 25 avenue du Québec, 91951 Les Ulis cedex, France.

出版信息

J Biol Chem. 2002 Jul 26;277(30):27120-9. doi: 10.1074/jbc.M203421200. Epub 2002 May 20.

Abstract

Apolipoprotein CIII (apoCIII) plays an important role in plasma triglyceride and remnant lipoprotein metabolism. Because hypertriglyceridemia is an independent risk factor in coronary artery disease and the presence in plasma of triglyceride-rich remnant lipoproteins is correlated with atherosclerosis, considerable research efforts have been focused on the identification of factors regulating apoCIII gene expression to decrease its production. Here we report that the orphan nuclear hormone receptor Rev-erbalpha regulates the human apoCIII gene promoter. In apoCIII expressing human hepatic HepG2 cells, transfection of Rev-erbalpha specifically repressed apoCIII gene promoter activity. We determined by deletion and site-directed mutagenesis experiments that Rev-erbalpha dependent repression is mainly due to an element present in the proximal promoter of the apoCIII gene. In contrast, we found no functional Rev-erbalpha response elements in the convergently transcribed human apoAI gene or the common regulatory enhancer. The identified Rev-erbalpha response element coincides with a RORalpha1 element, and in the present study we provide evidence that functional cross-talk between these orphan receptors modulates the apoCIII promoter. In vitro binding analysis showed that monomers of Rev-erbalpha bound this element but not another upstream RORalpha1 response element. In addition, we showed that the closely related nuclear orphan receptor RVR also specifically repressed the human apoCIII gene. These studies underscore a novel physiological role for members of the Rev-erb family of nuclear receptors in the regulation of genes involved in triglyceride metabolism and the pathogenesis of atherosclerosis.

摘要

载脂蛋白CIII(apoCIII)在血浆甘油三酯和残余脂蛋白代谢中起重要作用。由于高甘油三酯血症是冠状动脉疾病的独立危险因素,且富含甘油三酯的残余脂蛋白在血浆中的存在与动脉粥样硬化相关,因此大量研究致力于确定调节apoCIII基因表达以减少其产生的因素。在此我们报告,孤儿核激素受体Rev-erbalpha调节人apoCIII基因启动子。在表达apoCIII的人肝癌HepG2细胞中,转染Rev-erbalpha可特异性抑制apoCIII基因启动子活性。我们通过缺失和定点诱变实验确定,Rev-erbalpha依赖性抑制主要归因于apoCIII基因近端启动子中存在的一个元件。相反,我们在反向转录的人apoAI基因或共同调节增强子中未发现功能性Rev-erbalpha反应元件。所鉴定的Rev-erbalpha反应元件与一个RORalpha1元件重合,在本研究中我们提供证据表明这些孤儿受体之间的功能性相互作用调节apoCIII启动子。体外结合分析表明,Rev-erbalpha单体结合该元件,但不结合另一个上游RORalpha1反应元件。此外,我们表明密切相关的核孤儿受体RVR也特异性抑制人apoCIII基因。这些研究强调了Rev-erb家族核受体成员在调节参与甘油三酯代谢和动脉粥样硬化发病机制的基因方面的新生理作用。

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