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人类孤儿受体COUP-TFII通过降低hTERT转录来抑制端粒酶活性的证据。

The evidences of human orphan receptor COUP-TFII inhibiting telomerase activity through decreasing hTERT transcription.

作者信息

Wang Qiang, Bai Zengliang, Li Xuan, Hou Lin, Zhang Bo

机构信息

The provincial Key Laboratory of Mechanisms of Development and Gene Control, Life Science School of Shandong University, Jinan, China.

出版信息

Cancer Lett. 2004 Oct 8;214(1):81-90. doi: 10.1016/j.canlet.2004.03.032.

Abstract

Activation of hTERT, the human telomerase catalytic subunit, has been implicated as the critical event in triggering telomerase activity of cancer cells, but the details of regulation of hTERT need to be elucidated. By screening HeLa cDNA library with hTERT promoter-based yeast one-hybrid assay, one of positive clones, which potentially interacted with hTERT promoter, contained the full sequences of COUP-TFII cDNA. EMSA showed that the prepared His-tagged COUP-TFII could firmly bind to -201 to +35 fragment of hTERT promoter. The precise binding sites were confirmed by DNase I footprint analysis and proved to involve the E-box motif of hTERT promoter. Luciferase reporter assays indicated that COUP-TFII could suppress the transcription of hTERT promoter, and the inhibition to some extent could be reversed by co-transfection of c-myc. Stable introduction of COUP-TFII into HeLa cells decreased both endogenous hTERT expression and telomerase activity. The results suggested that the human COUP-TFII could specifically interact with hTERT promoter, in part via the E-box, and suppress the expression of hTERT.

摘要

人端粒酶催化亚基hTERT的激活被认为是触发癌细胞端粒酶活性的关键事件,但hTERT的调控细节仍有待阐明。通过基于hTERT启动子的酵母单杂交试验筛选HeLa cDNA文库,其中一个与hTERT启动子可能相互作用的阳性克隆包含COUP-TFII cDNA的完整序列。电泳迁移率变动分析表明所制备的His标签COUP-TFII能牢固结合到hTERT启动子的-201至+35片段。通过DNase I足迹分析确定了精确的结合位点,并证明其涉及hTERT启动子的E-box基序。荧光素酶报告基因试验表明COUP-TFII可抑制hTERT启动子的转录,并且通过共转染c-myc在一定程度上可逆转这种抑制作用。将COUP-TFII稳定导入HeLa细胞可降低内源性hTERT表达和端粒酶活性。结果表明人COUP-TFII可特异性地与hTERT启动子相互作用,部分通过E-box,并抑制hTERT的表达。

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