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转化生长因子-β2基因的转录依赖于位于该基因一个必需的环磷酸腺苷反应元件/激活转录因子基序与TATA盒之间的一个E盒。

Transcription of the transforming growth factor-beta2 gene is dependent on an E-box located between an essential cAMP response element/activating transcription factor motif and the TATA box of the gene.

作者信息

Scholtz B, Kingsley-Kallesen M, Rizzino A

机构信息

Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198-6805, USA.

出版信息

J Biol Chem. 1996 Dec 13;271(50):32375-80. doi: 10.1074/jbc.271.50.32375.

Abstract

Transforming growth factor-beta2 (TGF-beta2) is an important regulator of cell proliferation and differentiation; however, its transcriptional regulation is not well understood. Here we report characterization of an essential E-box motif, positioned at -50/-45 between a previously described functional cAMP response element/activating transcription factor site and the TATA box of the human TGF-beta2 promoter. By site-directed mutagenesis, we demonstrate that this E-box motif is necessary for the promoter activity, not only in differentiated cells derived from embryonal carcinoma cells, but also in choriocarcinoma cells and in MCF-7 breast carcinoma cells. We also demonstrate that the transcription factors USF1 and USF2 bind to this E-box motif in vitro when nuclear extracts from each of these cell lines are examined by gel retardation assays. Moreover, using a dominant-negative USF2 protein, we show that USF proteins are critical for TGF-beta2 promoter activity in vivo. The importance of the E-box motif described in this study is supported by the presence of an E-box motif in the same position in the chicken TGF-beta2 gene promoter.

摘要

转化生长因子-β2(TGF-β2)是细胞增殖和分化的重要调节因子;然而,其转录调控机制尚未完全明确。在此,我们报告了一个位于人TGF-β2启动子的功能性cAMP反应元件/激活转录因子位点与TATA盒之间-50/-45位置的关键E盒基序的特征。通过定点诱变,我们证明该E盒基序不仅对源自胚胎癌细胞的分化细胞中的启动子活性是必需的,而且对绒毛膜癌细胞和MCF-7乳腺癌细胞中的启动子活性也是必需的。当通过凝胶阻滞试验检测这些细胞系各自的核提取物时,我们还证明转录因子USF1和USF2在体外与该E盒基序结合。此外,使用显性负性USF2蛋白,我们表明USF蛋白在体内对TGF-β2启动子活性至关重要。鸡TGF-β2基因启动子中相同位置存在E盒基序,支持了本研究中所描述的E盒基序的重要性。

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