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鸡卵清蛋白上游启动子转录因子作为肝细胞核因子4的辅助共因子,增强肝脏基因表达。

Chicken ovalbumin upstream promoter transcription factors act as auxiliary cofactors for hepatocyte nuclear factor 4 and enhance hepatic gene expression.

作者信息

Ktistaki E, Talianidis I

机构信息

Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology Hellas, Herakleion, Crete, Greece.

出版信息

Mol Cell Biol. 1997 May;17(5):2790-7. doi: 10.1128/MCB.17.5.2790.

Abstract

Chicken ovalbumin upstream promoter transcription factors (COUP-TFs) strongly inhibit transcriptional activation mediated by nuclear hormone receptors, including hepatocyte nuclear factor 4 (HNF-4). COUP-TFs repress HNF-4-dependent gene expression by competition with HNF-4 for common binding sites found in several regulatory regions. Here we show that promoters, such as the HNF-1 promoter, which are recognized by HNF-4 but not by COUP-TFs are activated by COUP-TFI and COUP-TFII in conjunction with HNF-4 more than 100-fold above basal levels, as opposed to about 8-fold activation by HNF-4 alone. This enhancement was strictly dependent on an intact HNF-4 E domain. In vitro and in vivo evidence suggests that COUP-TFs enhance HNF-4 activity by a mechanism that involves their physical interaction with the amino acid 227 to 271 region of HNF-4. Our results indicate that in certain promoters, COUP-TFs act as auxiliary cofactors for HNF-4, orienting the HNF-4 activation domain in a more efficient configuration to achieve enhanced transcriptional activity. These findings provide new insights into the regulatory functions of COUP-TFs, suggesting their involvement in the initial activation and subsequent high-level expression of hepatic regulators, as well as in the positive and negative modulation of downstream target genes.

摘要

鸡卵清蛋白上游启动子转录因子(COUP-TFs)强烈抑制由核激素受体介导的转录激活,包括肝细胞核因子4(HNF-4)。COUP-TFs通过与HNF-4竞争在几个调控区域中发现的共同结合位点来抑制HNF-4依赖的基因表达。在这里我们表明,诸如HNF-1启动子等能被HNF-4识别但不能被COUP-TFs识别的启动子,在与HNF-4共同作用时,被COUP-TFI和COUP-TFII激活的程度比基础水平高出100倍以上,而单独由HNF-4激活时仅约为8倍。这种增强严格依赖于完整的HNF-4 E结构域。体外和体内证据表明,COUP-TFs通过一种涉及它们与HNF-4的227至271氨基酸区域进行物理相互作用的机制来增强HNF-4的活性。我们的结果表明,在某些启动子中,COUP-TFs作为HNF-4的辅助辅因子,将HNF-4激活结构域定向到更有效的构型以实现增强的转录活性。这些发现为COUP-TFs的调控功能提供了新的见解,表明它们参与肝脏调节因子的初始激活和随后的高水平表达,以及下游靶基因的正负调控。

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