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泛素结合酶9(Ubc9)与鸡卵清蛋白上游启动子转录因子I相互作用,并抑制受体依赖性转录。

Ubc9 interacts with chicken ovalbumin upstream promoter-transcription factor I and represses receptor-dependent transcription.

作者信息

Kobayashi S, Shibata H, Kurihara I, Yokota K, Suda N, Saito I, Saruta T

机构信息

Department of Internal Medicine, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

J Mol Endocrinol. 2004 Feb;32(1):69-86. doi: 10.1677/jme.0.0320069.

Abstract

Chicken ovalbumin upstream promoter-transcription factors (COUP-TFs) are orphan receptors involved in regulation of neurogenesis and organogenesis. COUP-TF family members are generally considered to be transcriptional repressors and several mechanisms have been proposed to underlie this activity. To explore novel transcriptional coregulators for COUP-TFs, we used the COUP-TFI as bait in a yeast two-hybrid screen of an adrenocortical adenoma cDNA library. We have identified Ubc9, a class E2 conjugating enzyme of small ubiquitin-related modifier (SUMO)-1 as a COUP-TFI corepressor. Ubc9 interacts with COUP-TFI in yeast and in glutathione S-transferase pulldown and coimmunoprecipitation assays. Fluorescence imaging studies show that both Ubc9 and COUP-TFI are colocalized in the nuclei of transfected COS-1 cells. The C-terminal region of Ubc9 encoding amino acids 59-158 interacts with the C-terminus of COUP-TFI encoding amino acids 383-403, in which transcriptional repression domains are located. Mammalian one-hybrid assays utilizing a variety of Ubc9 fragments fused to Gal4 DNA-binding domain show that a Ubc9 fragment encoding amino acids 1-89 contains autonomous transferrable repression domain. Transfection of Ubc9 into COS-1 cells markedly enhances transcriptional repression by Gal4 DNA-binding domain-fused to COUP-TFI(155-423), but not by Gal4-COUP-TFI(155-388) which lacks a repressor domain. Coexpression of a C-terminal deletion mutant of Ubc9(1-58), which fails to interact with COUP-TFI, but retains a transcriptional repression domain, has no effect on Gal4-COUP-TFI-mediated repression activity. These findings indicate that interaction of Ubc9 with COUP-TFI is crucial for the corepressor function of Ubc9. Overexpression of Ubc9 similarly enhances COUP-TFI-dependent repression of the promoter activity of the bovine CYP17 gene encoding steroid 17alpha-hydroxylase. In addition, the C93S mutant of Ubc9, which abrogates SUMO-1 conjugation activity, continues to function as a COUP-TFI corepressor. Our studies indicate that Ubc9 functions as a novel COUP-TFI corepressor, the function of which is distinct from its SUMO-1 conjugating enzyme activity.

摘要

鸡卵清蛋白上游启动子转录因子(COUP-TFs)是参与神经发生和器官发生调控的孤儿受体。COUP-TF家族成员通常被认为是转录抑制因子,并且已经提出了几种机制来解释这种活性。为了探索COUP-TFs的新型转录共调节因子,我们在肾上腺皮质腺瘤cDNA文库的酵母双杂交筛选中使用COUP-TFI作为诱饵。我们鉴定出Ubc9,一种小泛素相关修饰物(SUMO)-1的E2类缀合酶,作为COUP-TFI的共抑制因子。Ubc9在酵母中以及在谷胱甘肽S-转移酶下拉和免疫共沉淀试验中与COUP-TFI相互作用。荧光成像研究表明,Ubc9和COUP-TFI都共定位于转染的COS-1细胞的细胞核中。Ubc9编码氨基酸59 - 158的C末端区域与COUP-TFI编码氨基酸383 - 403的C末端相互作用,转录抑制结构域位于该区域。利用与Gal4 DNA结合结构域融合的各种Ubc9片段进行的哺乳动物单杂交试验表明,编码氨基酸1 - 89的Ubc9片段含有自主可转移的抑制结构域。将Ubc9转染到COS-1细胞中显著增强了与COUP-TFI(155 - 423)融合的Gal4 DNA结合结构域的转录抑制作用,但对缺乏抑制结构域的Gal4 - COUP-TFI(155 - 388)没有增强作用。与COUP-TFI不相互作用但保留转录抑制结构域的Ubc9(1 - 58)的C末端缺失突变体的共表达,对Gal4 - COUP-TFI介导的抑制活性没有影响。这些发现表明,Ubc9与COUP-TFI的相互作用对于Ubc9的共抑制因子功能至关重要。Ubc9的过表达同样增强了COUP-TFI对编码类固醇17α-羟化酶的牛CYP17基因启动子活性的依赖性抑制作用。此外,消除SUMO-1缀合活性的Ubc9的C93S突变体继续作为COUP-TFI的共抑制因子发挥作用。我们的研究表明,Ubc9作为一种新型的COUP-TFI共抑制因子发挥作用,其功能与其SUMO-1缀合酶活性不同。

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