2010
DOI: 10.1158/1541-7786.mcr-09-0141
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Repression of Human Telomerase Reverse Transcriptase Using Artificial Zinc Finger Transcription Factors

Abstract: 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 t… Show more

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Cited by 13 publications
(8 citation statements)
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“…Bioluminescent reporters are regularly used to study the regulation of gene expression by cis- or trans-acting factors, such as gene regulatory elements[1], transcription factors[2], or exogenous regulators[3]. Luciferase enzymes have also been used for tracking cell migration[4] in living subjects and monitoring intracellular molecular interactions[5].…”
Section: Introductionmentioning
confidence: 99%
“…Bioluminescent reporters are regularly used to study the regulation of gene expression by cis- or trans-acting factors, such as gene regulatory elements[1], transcription factors[2], or exogenous regulators[3]. Luciferase enzymes have also been used for tracking cell migration[4] in living subjects and monitoring intracellular molecular interactions[5].…”
Section: Introductionmentioning
confidence: 99%
“…An artificial transcriptional zinc-finger-mediated upregulation of telomerase activity through epigenetic mechanisms specifically in satellite cells could perhaps lead to increased self-renewal such that the stem cells do not become depleted as the need for repair continues over the lifetime of the patient. A similar approach has recently been explored to repress expression of telomerase in transformed cells using artificial zinc fingers fused to the transcriptional repressor domain of KRAB [71]. Epigenetic enzymes could thus represent a viable target for future gene therapies to permit muscle repair in muscular dystrophy patients.…”
Section: Modulating Epigenetics As a Therapeutic Approach To Muscularmentioning
confidence: 99%
“…Recently regulated genes include: mammary serine protease inhibitor (maspin) [103,118], dystrophin-related gene utrophin [119], vascular endothelial growth factor A (VEGF-A) [120,121], gamma-globin [122], heme oxygenase-1 gene (HMOX1) [123], glial cell line-derived neurotrophic factor gene (GDNF) [124], derived tyrosine kinase receptors ErbB2 [90,125], and ErbB3 [100,125]. Genes that were successfully downregulated by ATFs comprise: VEGF-A [120,121], ErbB2 [90,125], ErbB3 [100], the human telomerase reverse transcriptase (hTERT) [126], the nuclear hormone receptor PPARγ gene (PPARγ) [127], and the repression of the checkpoint kinase 2 (CHK2) gene [88]. The most recent application of engineered ZF DBDs embrace the ability to specifically modify the genome using zinc finger nucleases (ZFNs).…”
Section: Design Of the Dna Binding Domain (Dbd)mentioning
confidence: 99%