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肾上腺类固醇生成中的COUP-TF与转录共调节因子

COUP-TF and transcriptional co-regulators in adrenal steroidogenesis.

作者信息

Shibata Hirotaka, Kobayashi Sakiko, Kurihara Isao, Suda Noriko, Yokota Kenichi, Murai Ayano, Ikeda Yayoi, Saito Ikuo, Rainey William E, Saruta Takao

机构信息

Health Center, Keio University, Tokyo, Japan.

出版信息

Endocr Res. 2004 Nov;30(4):795-801. doi: 10.1081/erc-200044042.

Abstract

Chicken ovalbumin upstream promoter-transcription factors (COUP-TFs) and steroidogenic factor-1 (SF-1) play key roles in the transcriptional regulation of steroidogenic P450 genes. Transfection studies showed that SF-1 activated bovine CYP17 promoter activity, whereas COUP-TFs repressed it from the CRS2 element in a mutually exclusive manner in mouse adrenocortical Y-1 cells. COUP-TFI and SF-1 competitively bind to the Ad5 element of the human CYP11B2 gene promoter. Unexpectedly, overexpression of COUP-TFI increased the CYP11B2 promoter activity, whereas overexpression of SF-1 repressed it in human adrenocortical H295R cells. In cortisol-producing adrenal cortical adenomas, down-regulation of nuclear receptors, including COUP-TFs was found. We therefore screened for COUP-TFI-interacting proteins using a yeast two-hybrid system and have identified Ubc9 and PIAS1, SUMO-1 conjugating enzyme and ligase, respectively. Coexpression of Ubc9 and PIAS1 synergistically enhanced COUP-TFI-mediated trans-repression of CYP17 gene as well as transactivation of CYP11B2 gene. The SUMOylation-defective mutants of these proteins continued to function as co-regulators of COUP-TFI. These findings indicate that Ubc9 and PIAS1 can function as transcriptional co-regulators of COUP-TFI to modulate adrenal cortical steroidogenesis in a SUMOylation-independent manner.

摘要

鸡卵清蛋白上游启动子转录因子(COUP-TFs)和类固醇生成因子-1(SF-1)在类固醇生成性细胞色素P450基因的转录调控中起关键作用。转染研究表明,SF-1激活牛CYP17启动子活性,而在小鼠肾上腺皮质Y-1细胞中,COUP-TFs以互斥方式从CRS2元件抑制该活性。COUP-TFI和SF-1竞争性结合人CYP11B2基因启动子的Ad5元件。出乎意料的是,在人肾上腺皮质H295R细胞中,COUP-TFI的过表达增加了CYP11B2启动子活性,而SF-1的过表达则抑制了该活性。在产生皮质醇的肾上腺皮质腺瘤中,发现包括COUP-TFs在内的核受体下调。因此,我们使用酵母双杂交系统筛选了与COUP-TFI相互作用的蛋白,分别鉴定出泛素结合酶9(Ubc9)和小泛素样修饰蛋白1(SUMO-1)连接酶PIAS1。Ubc9和PIAS1的共表达协同增强了COUP-TFI介导的对CYP17基因的反式抑制以及对CYP11B2基因的反式激活。这些蛋白的SUMO化缺陷突变体继续作为COUP-TFI的共调节因子发挥作用。这些发现表明,Ubc9和PIAS1可以作为COUP-TFI的转录共调节因子,以不依赖SUMO化的方式调节肾上腺皮质类固醇生成。

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