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解偶联蛋白基因中的一个复杂视黄酸反应元件确定了类视黄醇在产热中的新作用。

A complex retinoic acid response element in the uncoupling protein gene defines a novel role for retinoids in thermogenesis.

作者信息

Rabelo R, Reyes C, Schifman A, Silva J E

机构信息

Department of Medicine, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada.

出版信息

Endocrinology. 1996 Aug;137(8):3488-96. doi: 10.1210/endo.137.8.8754778.

Abstract

Retinoids have been implicated in the control of cell proliferation and differentiation, and in several developmental processes. We report here the molecular bases for a metabolic role of RA, by showing that the expression of the uncoupling protein (UCP), the key element in brown adipose tissue (BAT) thermogenesis, is stimulated by retinoic acid (RA). Both all-trans-RA and 9-cis-RA powerfully increase UCP messenger RNA levels in isolated rat brown adipocytes. Transient transfection experiments in HIB-1B cells, a BAT-derived cell line, identified the sequence -2399/-2490 (called R90) as the RA-responsive sequence in the rat UCP gene. R90 mediated a 20- to 70-fold stimulation of the chloramphenicol acetyl transferase reporter gene by maximal concentrations of all-trans-RA or 9-cis-RA. Non-BAT cells were significantly less responsive. RA effect was also less when chloramphenicol acetyl transferase gene was driven by a heterologous promoter instead of the UCP minimal promoter. By footprinting and site-directed mutagenesis, we identified three discrete sequences as being essential for the RA response within R90, thus defining the complex RA response element (RARE) of this gene. Critical bases in these sequences are arranged in pairs of putative half-sites. RAR gamma-RXR heterodimers can bind to the R90 as revealed by electrophoretic mobility shift assays using in vitro translated receptors, and HIB-1B nuclear extracts with anti-RAR gamma or anti-RXR antibodies. The participation of RAR gamma-RXR heterodimers in RA stimulation is further supported by transient transfection experiments overexpressing selected receptors and dose-response analyses of RA isomers and analogues. These results show that retinoids strongly stimulate the rat UCP gene expression through a complex RARE, composed of three pairs of half-sites, and define a novel role for retinoids in the regulation of facultative thermogenesis and energy expenditure.

摘要

维甲酸与细胞增殖和分化的调控以及多个发育过程有关。我们在此报告视黄酸(RA)代谢作用的分子基础,通过证明棕色脂肪组织(BAT)产热的关键元件解偶联蛋白(UCP)的表达受视黄酸(RA)刺激。全反式视黄酸(all-trans-RA)和9-顺式视黄酸(9-cis-RA)均能有力地提高分离的大鼠棕色脂肪细胞中UCP信使核糖核酸水平。在源自BAT的细胞系HIB-1B细胞中进行的瞬时转染实验确定,序列-2399/-2490(称为R90)为大鼠UCP基因中的视黄酸反应序列。R90介导在全反式视黄酸或9-顺式视黄酸最大浓度作用下氯霉素乙酰转移酶报告基因20至70倍的刺激。非BAT细胞的反应明显较弱。当氯霉素乙酰转移酶基因由异源启动子而非UCP最小启动子驱动时,视黄酸的作用也较小。通过足迹法和定点诱变,我们确定了三个离散序列是R90内视黄酸反应所必需的,从而确定了该基因的复杂视黄酸反应元件(RARE)。这些序列中的关键碱基以假定的半位点对形式排列。如使用体外翻译受体以及用抗RARγ或抗RXR抗体处理的HIB-1B细胞核提取物进行的电泳迁移率变动分析所揭示,RARγ-RXR异二聚体可与R90结合。过表达选定受体的瞬时转染实验以及视黄酸异构体和类似物的剂量反应分析进一步支持了RARγ-RXR异二聚体参与视黄酸刺激。这些结果表明,维甲酸通过由三对半位点组成的复杂RARE强烈刺激大鼠UCP基因表达,并确定了维甲酸在兼性产热和能量消耗调节中的新作用。

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