Burris T P, Nawaz Z, Tsai M J, O'Malley B W
Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9525-9. doi: 10.1073/pnas.92.21.9525.
Nuclear hormone receptors are transcription factors that require multiple protein-protein interactions to regulate the expression of their target genes. Using the yeast two-hybrid system, we identified a protein, thyroid hormone receptor uncoupling protein (TRUP), that specifically interacts with a region of the human thyroid hormone receptor (TR) consisting of the hinge region and the N-terminal portion of the ligand binding domain in a hormone-independent manner. Interestingly, TRUP inhibits transactivation by TR and the retinoic acid receptor but has no effect on the estrogen receptor or the retinoid X receptor in mammalian cells. We also demonstrate that TRUP exerts its action on TR and retinoic acid receptor by interfering with their abilities to interact with their DNA. TRUP represents a type of regulatory protein that modulates the transcriptional activity of a subclass of the nuclear hormone receptor superfamily by preventing interaction with their genomic response elements.
核激素受体是一类转录因子,它们需要多种蛋白质-蛋白质相互作用来调节其靶基因的表达。利用酵母双杂交系统,我们鉴定出一种蛋白质,即甲状腺激素受体解偶联蛋白(TRUP),它以激素非依赖的方式与人类甲状腺激素受体(TR)中由铰链区和配体结合域的N端部分组成的区域特异性相互作用。有趣的是,TRUP在哺乳动物细胞中抑制TR和视黄酸受体的反式激活,但对雌激素受体或视黄酸X受体没有影响。我们还证明,TRUP通过干扰TR和视黄酸受体与DNA相互作用的能力来发挥其作用。TRUP代表一种调节蛋白,它通过阻止与基因组反应元件的相互作用来调节核激素受体超家族一个亚类的转录活性。