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Identification and characterization of negative regulatory elements of the human telomerase catalytic subunit (hTERT) gene promoter: possible role of MZF-2 in transcriptional repression of hTERT

机译:鉴定和表征人类端粒酶催化亚基(hTERT)基因启动子的负调控元件:MZF-2在hTERT转录抑制中的可能作用

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摘要

Human telomerase reverse transcriptase (hTERT) is a catalytic subunit of human telomerase and is a critical determinant of the enzymatic activity of telomerase. Expression of hTERT is known to be regulated mainly at the transcriptional level. In the present study, using transient expression assays, we identified a 400 bp silencer of the hTERT promoter between –776 and –378 upstream of the proximal core promoter. The inhibitory effects of this silencer were enhanced with cellular differentiation. A computer-assisted homology search identified multiple binding motifs for myeloid-specific zinc finger protein 2 (MZF-2) within this region. Mutation introduced in these sites resulted in significant activation of hTERT transcription. Gel shift assays demonstrated that MZF-2 proteins specifically bound to these sites. Overexpression of MZF-2 in cells led to down-regulation of hTERT transcription as well as telomerase activity. These findings suggest that the 400 bp region upstream of the hTERT core promoter that we identified functions as a negative regulatory region and that MZF-2 may be an effector of negative regulation of hTERT.
机译:人端粒酶逆转录酶(hTERT)是人端粒酶的催化亚基,并且是端粒酶酶活性的关键决定因素。已知hTERT的表达主要在转录水平受到调控。在本研究中,我们使用瞬时表达测定法,在近端核心启动子上游–776和–378之间鉴定了hTERT启动子的400 bp沉默子。细胞分化增强了该沉默子的抑制作用。计算机辅助同源性搜索确定了该区域内髓样特异性锌指蛋白2(MZF-2)的多个结合基序。在这些位点引入的突变导致hTERT转录的显着激活。凝胶位移分析表明,MZF-2蛋白与这些位点特异性结合。 MZF-2在细胞中的过表达导致hTERT转录以及端粒酶活性的下调。这些发现表明,我们确定的hTERT核心启动子上游的400 bp区域起着负调控区域的作用,而MZF-2可能是hTERT负调控的效应子。

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