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肾母细胞瘤1抑癌基因可抑制人端粒酶逆转录酶基因的转录。

The Wilms' tumor 1 tumor suppressor gene represses transcription of the human telomerase reverse transcriptase gene.

作者信息

Oh S, Song Y, Yim J, Kim T K

机构信息

National Creative Research Initiative Center for Genetic Reprogramming, Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Korea.

出版信息

J Biol Chem. 1999 Dec 24;274(52):37473-8. doi: 10.1074/jbc.274.52.37473.

Abstract

Regulation of the human telomerase reverse transcriptase (hTERT) gene is the primary determinant for telomerase enzyme activity, which is found in tumor cells but is largely absent from normal somatic cells. Recent studies have shown that Myc protein can transcriptionally activate the hTERT gene. However, little is known about the repression mechanism of the hTERT gene and telomerase enzyme. Here, we developed an expression cloning strategy to identify cDNAs whose products can repress hTERT promoter activity in telomerase-positive immortal cells. Using this screen, we isolated the Wilms' tumor 1 suppressor gene (WT1). WT1 can repress hTERT promoter activity in 293 kidney cells. The WT1 binding site on the hTERT promoter was identified by deletional analysis. Alteration of the WT1 binding site markedly derepresses transcription from an isolated hTERT promoter by inhibiting interaction of WT1 with DNA. These specific repression effects of WT1 were not observed in HeLa cells, which express no endogenous WT1. Furthermore, we show that WT1 can repress the endogenous hTERT promoter and telomerase enzyme activities. These results suggest that WT1 may be a transcriptional repressor of the hTERT gene, at least in some specific cells.

摘要

人类端粒酶逆转录酶(hTERT)基因的调控是端粒酶活性的主要决定因素,端粒酶活性在肿瘤细胞中存在,但在正常体细胞中基本不存在。最近的研究表明,Myc蛋白可以转录激活hTERT基因。然而,关于hTERT基因和端粒酶的抑制机制知之甚少。在这里,我们开发了一种表达克隆策略,以鉴定其产物能够抑制端粒酶阳性永生化细胞中hTERT启动子活性的cDNA。通过该筛选,我们分离出了威尔姆斯瘤1抑制基因(WT1)。WT1可以抑制293肾细胞中的hTERT启动子活性。通过缺失分析确定了hTERT启动子上的WT1结合位点。WT1结合位点的改变通过抑制WT1与DNA的相互作用,显著解除了从分离的hTERT启动子的转录抑制。在不表达内源性WT1的HeLa细胞中未观察到WT1的这些特异性抑制作用。此外,我们表明WT1可以抑制内源性hTERT启动子和端粒酶活性。这些结果表明,WT1可能是hTERT基因的转录抑制因子,至少在某些特定细胞中是如此。

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