Masuyama H, Brownfield C M, St-Arnaud R, MacDonald P N
Department of Pharmacological and Physiological Science, Saint Louis University Health Science Center, Missouri 63104, USA.
Mol Endocrinol. 1997 Sep;11(10):1507-17. doi: 10.1210/mend.11.10.9990.
A ligand-dependent transcriptional activation domain (AF-2) exists in region E of the nuclear receptors. This highly conserved domain may contact several coactivators that are putatively involved in nuclear receptor-mediated transcription. In this study, a panel of vitamin D receptor (VDR) AF-2 mutants was created to examine the importance of several conserved residues in VDR-activated transcription. Two AF-2 mutants (L417S and E420Q) exhibited normal ligand binding, heterodimerization with retinoid X receptor, and vitamin D-responsive element interaction, but they were transcriptionally inactive in a VDR-responsive reporter gene assay. All AF-2 mutations that abolished VDR-mediated transactivation also eliminated interactions between VDR and several putative coactivator proteins including suppressor of gal1 (SUG1), steroid hormone receptor coactivator-1 (SRC-1), or receptor interacting protein (RIP140), suggesting that coactivator interaction is important for AF-2-mediated transcription. In support of this concept, the minimal AF-2 domain [VDR(408-427)] fused to the gal4 DNA binding domain was sufficient to mediate transactivation as well as interaction with putative coactivators. Introducing the L417S and E420Q mutations into the minimal AF-2 domain abolished this autonomous transactivation and coactivator interactions. Finally, we demonstrate that the minimal AF-2 domain interacted with an AF-2 deletion mutant of the VDR in a 1,25-(OH)2D3-dependent manner, suggesting a ligand-induced intramolecular folding of the VDR AF-2 domain. The L417S mutant of this domain disrupted the interaction with VDR ligand-binding domain, while the E420Q mutant did not affect this interaction. These studies suggest that the conserved AF-2 motif may mediate transactivation through ligand-dependent intermolecular interaction with coactivators and through ligand-induced intramolecular contacts with the VDR ligand-binding domain itself.
核受体的E区域存在一个配体依赖性转录激活结构域(AF-2)。这个高度保守的结构域可能与几种推测参与核受体介导转录的共激活因子相互作用。在本研究中,构建了一组维生素D受体(VDR)AF-2突变体,以研究VDR激活转录过程中几个保守残基的重要性。两个AF-2突变体(L417S和E420Q)表现出正常的配体结合、与视黄酸X受体的异源二聚化以及维生素D反应元件相互作用,但在VDR反应性报告基因检测中它们转录无活性。所有消除VDR介导的反式激活的AF-2突变也消除了VDR与几种推测的共激活因子蛋白之间的相互作用,这些共激活因子蛋白包括gal1抑制因子(SUG1)、类固醇激素受体共激活因子-1(SRC-1)或受体相互作用蛋白(RIP140),这表明共激活因子相互作用对AF-2介导的转录很重要。支持这一概念的是,与gal4 DNA结合结构域融合的最小AF-2结构域[VDR(408 - 427)]足以介导反式激活以及与推测的共激活因子的相互作用。将L417S和E420Q突变引入最小AF-2结构域可消除这种自主反式激活和共激活因子相互作用。最后,我们证明最小AF-2结构域以1,25-(OH)2D3依赖性方式与VDR的AF-2缺失突变体相互作用,这表明VDR AF-2结构域存在配体诱导的分子内折叠。该结构域的L417S突变破坏了与VDR配体结合结构域的相互作用,而E420Q突变不影响这种相互作用。这些研究表明,保守的AF-2基序可能通过与共激活因子的配体依赖性分子间相互作用以及通过与VDR配体结合结构域本身的配体诱导分子内接触来介导反式激活。