Nakai A, Nagasaka A
Department of Internal Medicine, Fujita Health University School of Medicine.
Nihon Rinsho. 1994 Apr;52(4):916-21.
Thyroid hormone receptor (THR) binds to specific thyroid hormone response element (TRE). Using an electrophoretic mobility shift assay (gel-shift), Murray and Towel recently found that cell nuclear extracts enhance the binding of THR to TRE. This protein has been designated T3 receptor auxiliary protein (TRAP). Retinoid X receptors (RXR alpha, beta) can function as TRAP. TRAP forms a heterodimer with THR through the ligand binding domain of both receptors. This area contains leucine zipper like heptad repeats which can form amphipathic alpha-helixes. The ligand (9-cis retinoic acid) of RXR may or may not synergistically increase T3/THR-mediated transactivation. The effects of 9-cis retinoic acid depends on the nature of the TRE. One of the functions of TRAP may be to alter the expression of T3-regulated genes.
甲状腺激素受体(THR)与特定的甲状腺激素反应元件(TRE)结合。默里和托韦尔最近利用电泳迁移率变动分析(凝胶迁移)发现,细胞核提取物可增强THR与TRE的结合。这种蛋白质被命名为T3受体辅助蛋白(TRAP)。维甲酸X受体(RXRα、β)可作为TRAP发挥作用。TRAP通过两个受体的配体结合域与THR形成异源二聚体。该区域包含类似亮氨酸拉链的七肽重复序列,可形成两亲性α螺旋。RXR的配体(9-顺式维甲酸)可能协同增加也可能不协同增加T3/THR介导的反式激活。9-顺式维甲酸的作用取决于TRE的性质。TRAP的功能之一可能是改变T3调控基因的表达。