Shibata H, Nawaz Z, Tsai S Y, O'Malley B W, Tsai M J
Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Mol Endocrinol. 1997 Jun;11(6):714-24. doi: 10.1210/mend.11.6.0002.
Chicken ovalbumin upstream promoter-transcription factors (COUP-TFs) are orphan receptors that belong to the steroid/thyroid hormone receptor (TR) superfamily and can repress the transcriptional activity of several target genes; however, the precise mechanism of this repression is unknown. Transfection of a Gal4 DNA-binding domain fused to the putative ligand-binding domain of COUP-TFI (Gal4-COUP-TFI) significantly represses the basal transcriptional activity of a reporter gene containing Gal4-binding sites. Cotransfection of COUP-TFI can relieve the Gal4-COUP-TFI repression in a dose-dependent manner. In contrast, COUP-TFI delta35, which lacks the repressor domain (the C-terminal 35 amino acids), fails to relieve this repression. This finding suggests that the repressor domain of COUP-TFI may squelch a limiting amount of corepressor in HeLa cells. In addition, increasing concentrations of TRbeta also can relieve the COUP-TFI repression in a hormone-sensitive manner. Similarly, overexpression of increasing concentration of COUP-TFI, but not COUP-TFI delta35, can squelch the silencing activity of the unliganded TRbeta. Collectively, these results indicate that COUP-TFI and TRbeta share a common corepressor(s) for their silencing activity. To determine which corepressor is involved in the COUP-TF-silencing activity, we used a yeast two-hybrid and in vitro GST pull-down assays to demonstrate that COUP-TFI can interact with the fragment of N-CoR (nuclear receptor-corepressor) encoding amino acids 921-2453 and the fragments of SMRT (silencing mediator for retinoic acid receptor and TR) encoding amino acids 29-564 and 565-1289, respectively. Interestingly, the fragment of SMRT encoding amino acids 1192-1495, which strongly interacts with TRbeta, interacts very weakly with COUP-TFI. Furthermore, overexpression of N-CoR or SMRT potentiates the silencing activity of COUP-TFI and can relieve the COUP-TFI-mediated squelching of Gal4-COUP-TFI activity. Therefore, our studies indicate that N-CoR and SMRT act as corepressors for the COUP-TFI silencing activity.
鸡卵清蛋白上游启动子转录因子(COUP-TFs)是属于类固醇/甲状腺激素受体(TR)超家族的孤儿受体,能够抑制多个靶基因的转录活性;然而,这种抑制的确切机制尚不清楚。将与COUP-TFI假定配体结合域融合的Gal4 DNA结合域(Gal4-COUP-TFI)转染,可显著抑制含有Gal4结合位点的报告基因的基础转录活性。共转染COUP-TFI能够以剂量依赖的方式缓解Gal4-COUP-TFI的抑制作用。相比之下,缺少抑制结构域(C末端35个氨基酸)的COUP-TFI delta35无法缓解这种抑制作用。这一发现表明,COUP-TFI的抑制结构域可能会消耗HeLa细胞中有限量的共抑制因子。此外,增加TRbeta的浓度也能够以激素敏感的方式缓解COUP-TFI的抑制作用。同样,增加浓度的COUP-TFI(而非COUP-TFI delta35)的过表达能够抑制未结合配体的TRbeta的沉默活性。总体而言,这些结果表明,COUP-TFI和TRbeta在其沉默活性方面共享一种共同的共抑制因子。为了确定哪种共抑制因子参与了COUP-TF的沉默活性,我们使用酵母双杂交和体外GST下拉实验来证明,COUP-TFI能够分别与编码氨基酸921 - 2453的N-CoR(核受体共抑制因子)片段以及编码氨基酸29 - 564和565 - 1289的SMRT(视黄酸受体和TR的沉默介质)片段相互作用。有趣的是,与TRbeta强烈相互作用的编码氨基酸1192 - 1495的SMRT片段与COUP-TFI的相互作用非常弱。此外,N-CoR或SMRT的过表达增强了COUP-TFI的沉默活性,并能够缓解COUP-TFI介导的对Gal4-COUP-TFI活性的抑制作用。因此,我们的研究表明,N-CoR和SMRT作为COUP-TFI沉默活性的共抑制因子发挥作用。