Yang Yue, Wang Xin, Dong Tiefei, Kim Eungseok, Lin Wen-Jye, Chang Chawnshang
George Whipple Laboratory for Cancer Research Department of Pathology, University of Rochester Medical Center, Rochester, New York 14642, USA.
J Biol Chem. 2003 Feb 28;278(9):7709-17. doi: 10.1074/jbc.M207116200. Epub 2002 Dec 16.
Although many co-activators have been identified for various nuclear receptors, relatively fewer co-repressors have been isolated and characterized. Here we report the identification of a novel testicular orphan nuclear receptor-4 (TR4)-associated protein (TRA16) that is mainly localized in the nucleus of cells as a repressor to suppress TR4-mediated transactivation. The suppression of TR4-mediated transactivation is selective because TRA16 shows only a slight influence on the transactivation of androgen receptor, glucocorticoid receptor, and progesterone receptor. Sequence analysis shows that TRA16 is a novel gene with 139 amino acids in an open reading frame with a molecular mass of 16 kDa, which did not match any published gene sequences. Mammalian two-hybrid system and co-immunoprecipitation assays both demonstrate that TRA16 can interact strongly with TR4. The electrophoretic mobility shift assay suggests that TRA16 may suppress TR4-mediated transactivation via decreased binding between the TR4 protein and the TR4 response element on the target gene(s). Furthermore, TRA16 can also block the interaction between TR4 and TR4 ligand-binding domain through interacting with TR4-DNA-binding and ligand-binding domains. These unique suppression mechanisms suggest that TRA16 may function as a novel repressor to selectively suppress the TR4-mediated transactivation.
尽管已经鉴定出许多针对各种核受体的共激活因子,但相对较少的共抑制因子被分离和表征。在此,我们报告鉴定了一种新型的睾丸孤儿核受体4(TR4)相关蛋白(TRA16),它主要定位于细胞核中,作为一种抑制因子抑制TR4介导的反式激活。TRA16对TR4介导的反式激活的抑制具有选择性,因为它对雄激素受体、糖皮质激素受体和孕激素受体的反式激活仅产生轻微影响。序列分析表明,TRA16是一个新基因,其开放阅读框中有139个氨基酸,分子量为16 kDa,与任何已发表的基因序列均不匹配。哺乳动物双杂交系统和免疫共沉淀实验均表明,TRA16能与TR4强烈相互作用。电泳迁移率变动分析表明,TRA16可能通过减少TR4蛋白与靶基因上的TR4反应元件之间的结合来抑制TR4介导的反式激活。此外,TRA16还可通过与TR4的DNA结合域和配体结合域相互作用,阻断TR4与TR4配体结合域之间的相互作用。这些独特的抑制机制表明,TRA16可能作为一种新型抑制因子,选择性地抑制TR4介导的反式激活。