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Repression of human telomerase reverse transcriptase using artificial zinc finger transcription factors.

机译:使用人工锌指转录因子抑制人端粒酶逆转录酶。

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Telomerase activation is a key step in the development of human cancers. Expression of the catalytic subunit, human telomerase reverse transcriptase (hTERT), represents the limiting factor for telomerase activity. In this study, we have used artificial zinc finger protein (ZFP) transcription factors (TF) to repress the expression of hTERT in human cancer cell lines at the transcriptional level. We have constructed four-fingered ZFPs derived from the human genome which binds 12-bp recognition sequences within the promoter of the hTERT gene and fused them with a KRAB repressor domain to create a potent transcriptional repressor. Luciferase activity was decreased by >80% in all of the transcriptional repressors with luciferase reporter assay. When they were transfected into the telomerase-positive HEK293 cell line, a decrease of mRNA level and telomerase activity together with shortening of telomere length was observed. Actual growth of HEK293 cells was also inhibited by transfection of artificial ZFP-TFs. The repression was maintained for 100 days of culture. The repression of telomerase expression by artificial ZFP-TFs targeting the promoter region of the hTERT presents a new promising strategy for inhibiting the growth of human cancer cells.
机译:端粒酶激活是人类癌症发展的关键步骤。催化亚基,人类端粒酶逆转录酶(hTERT)的表达代表了端粒酶活性的限制因素。在这项研究中,我们已使用人工锌指蛋白(ZFP)转录因子(TF)在转录水平上抑制hTERT在人类癌细胞系中的表达。我们已经构建了源自人类基因组的四指ZFP,该ZFP结合hTERT基因启动子内的12 bp识别序列,并将其与KRAB阻遏物域融合,以创建有效的转录阻遏物。使用萤光素酶报告基因测定,所有转录阻遏物的萤光素酶活性均降低> 80%。当将它们转染到端粒酶阳性的HEK293细胞系中时,观察到mRNA水平和端粒酶活性的降低,以及端粒长度的缩短。人工ZFP-TF的转染也抑制了HEK293细胞的实际生长。压制维持100天的培养。靶向hTERT启动子区域的人工ZFP-TF抑制端粒酶表达,为抑制人类癌细胞的生长提供了一种新的有希望的策略。

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