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未结合配体的甲状腺激素受体β介导的转录沉默需要一种可溶性共抑制因子,该因子与受体的配体结合结构域相互作用。

Transcriptional silencing by unliganded thyroid hormone receptor beta requires a soluble corepressor that interacts with the ligand-binding domain of the receptor.

作者信息

Tong G X, Jeyakumar M, Tanen M R, Bagchi M K

机构信息

Population Council and the Rockefeller University, New York, NY 10021, USA.

出版信息

Mol Cell Biol. 1996 May;16(5):1909-20. doi: 10.1128/MCB.16.5.1909.

Abstract

Unliganded thyroid hormone receptor (TR) functions as a transcriptional repressor of genes bearing thyroid hormone response elements in their promoters. Binding of hormonal ligand to the receptor releases the transcriptional silencing and leads to gene activation. Previous studies showed that the silencing activity of TR is located within the C-terminal ligand-binding domain (LBD) of the receptor. To dissect the role of the LBD in receptor-mediated silencing, we used a cell-free transcription system containing HeLa nuclear extracts in which exogenously added unliganded TRbeta repressed the basal level of RNA polymerase II-driven transcription from a thyroid hormone response element-linked template. We designed competition experiments with a peptide fragment containing the entire LBD (positions 145 to 456) of TRbeta. This peptide, which lacks the DNA-binding domain, did not affect basal RNA synthesis from the thyroid hormone response element-linked promoter when added to a cell-free transcription reaction mixture. However, the addition of the LBD peptide to a reaction mixture containing TRbeta led to a complete reversal of receptor-mediated transcriptional silencing in the absence of thyroid hormone. An LBD peptide harboring point mutations, which severely impair receptor dimerization, also inhibited efficiently the silencing activity of TR, indicating that the relief of repression by the LBD was not due to the sequestration of TR or its heterodimeric partner retinoid X receptor into inactive homo- or heterodimers. We postulate that the LBD peptide competed with TR for a regulatory molecule, termed a corepressor, that exists in the HeLa nuclear extracts and is essential for efficient receptor-mediated gene repression. We have identified the region from positions 145 to 260 (the D domain) of the LBD as a potential binding site of the putative corepressor. We observed further that a peptide containing the LBD of retinoic acid receptor (RAR) competed for TR-mediated silencing, suggesting that the RAR LBD may bind to the same corepressor activity as the TR LBD. Interestingly, the RAR LBD complexed with its cognate ligand, all-trans retinoic acid, failed to compete for transcriptional silencing by TRbeta, indicating that the association of the LBD with the corepressor is ligand dependent. Finally, we provide strong biochemical evidence supporting the existence of the corepressor activity in the HeLa nuclear extracts. Our studies demonstrated that the silencing activity of TR was greatly reduced in the nuclear extracts preincubated with immobilized, hormone-free glutathione S-transferase-LBD fusion proteins, indicating that the corepressor activity was depleted from these extracts through protein-protein interactions with the LBD. Similar treatment with immobilized, hormone-bound glutathione S-transferase-LBD, on the other hand, failed to deplete the corepressor activity from the nuclear extracts, indicating that ligand binding to the LBD disrupts its interaction with the corepressor. From these results, we propose that a corepressor binds to the LBD of unliganded TR and critically influences the interaction of the receptor with the basal transcription machinery to promote silencing. Ligand binding to TR results in the release of the corepressor from the LBD and triggers the reversal of silencing by allowing the events leading to gene activation to proceed.

摘要

未结合配体的甲状腺激素受体(TR)作为一种转录抑制因子,作用于其启动子中带有甲状腺激素反应元件的基因。激素配体与受体的结合解除转录沉默并导致基因激活。先前的研究表明,TR的沉默活性位于受体的C末端配体结合结构域(LBD)内。为了剖析LBD在受体介导的沉默中的作用,我们使用了一个包含HeLa细胞核提取物的无细胞转录系统,其中外源添加的未结合配体的TRβ抑制了来自甲状腺激素反应元件连接模板的RNA聚合酶II驱动转录的基础水平。我们设计了与包含TRβ整个LBD(第145至456位)的肽片段的竞争实验。该肽缺乏DNA结合结构域,当添加到无细胞转录反应混合物中时,不影响来自甲状腺激素反应元件连接启动子的基础RNA合成。然而,将LBD肽添加到含有TRβ的反应混合物中导致在没有甲状腺激素的情况下受体介导的转录沉默完全逆转。携带严重损害受体二聚化的点突变的LBD肽也有效抑制了TR的沉默活性,表明LBD对抑制的解除不是由于TR或其异源二聚体伙伴视黄酸X受体被隔离成无活性的同二聚体或异二聚体。我们推测LBD肽与TR竞争一种调节分子,称为共抑制因子,它存在于HeLa细胞核提取物中,并且对于有效的受体介导的基因抑制至关重要。我们已经确定LBD的第145至260位区域(D结构域)是假定共抑制因子的潜在结合位点。我们进一步观察到,含有视黄酸受体(RAR)LBD的肽竞争TR介导的沉默,表明RAR LBD可能与与TR LBD相同的共抑制因子活性结合。有趣的是,与其同源配体全反式视黄酸复合的RAR LBD未能竞争TRβ介导的转录沉默,表明LBD与共抑制因子的结合是配体依赖性的。最后,我们提供了强有力的生化证据支持HeLa细胞核提取物中共抑制因子活性的存在。我们的研究表明,在用固定化的、无激素的谷胱甘肽S-转移酶-LBD融合蛋白预孵育的细胞核提取物中,TR的沉默活性大大降低,表明共抑制因子活性通过与LBD的蛋白质-蛋白质相互作用从这些提取物中耗尽。另一方面,用固定化的、结合激素的谷胱甘肽S-转移酶-LBD进行类似处理未能从细胞核提取物中耗尽共抑制因子活性,表明配体与LBD的结合破坏了其与共抑制因子的相互作用。从这些结果中,我们提出共抑制因子与未结合配体的TR的LBD结合,并严重影响受体与基础转录机制的相互作用以促进沉默。配体与TR的结合导致共抑制因子从LBD释放,并通过允许导致基因激活的事件进行来触发沉默的逆转。

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