Department of Biochemistry, Wonju College of Medicine, Yonsei University, Wonju, Republic of Korea.
Mol Cancer Res. 2010 Feb;8(2):246-53. doi: 10.1158/1541-7786.MCR-09-0141. Epub 2010 Feb 9.
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.
端粒酶激活是人类癌症发展的关键步骤。催化亚单位人端粒酶逆转录酶 (hTERT) 的表达代表端粒酶活性的限制因素。在这项研究中,我们使用人工锌指蛋白 (ZFP) 转录因子 (TF) 在转录水平上抑制人类癌细胞系中 hTERT 的表达。我们构建了源自人类基因组的四指 ZFP,它结合 hTERT 基因启动子内的 12 个碱基识别序列,并将其与 KRAB 抑制域融合,以创建一种有效的转录抑制剂。荧光素酶活性在所有转录抑制剂的荧光素酶报告基因检测中均降低了>80%。当它们被转染到端粒酶阳性的 HEK293 细胞系中时,观察到 mRNA 水平和端粒酶活性降低,以及端粒长度缩短。人工 ZFP-TFs 的转染也抑制了 HEK293 细胞的实际生长。抑制作用在 100 天的培养中得以维持。针对 hTERT 启动子区域的人工 ZFP-TFs 对端粒酶表达的抑制为抑制人类癌细胞生长提供了一种新的有前途的策略。