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Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering

机译:使用染色体工程技术在人类3p21.3染色体上定位hTERT阻遏物区域

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摘要

Telomerase is a ribonucleoprotein enzyme that synthesizes telomeric DNA. The reactivation of telomerase activity by aberrant upregulation/expression of its catalytic subunit hTERT is a major pathway in human tumorigenesis. However, regulatory mechanisms that control hTERT expression are largely unknown. Previously, we and others have demonstrated that the introduction of human chromosome 3, via microcell-mediated chromosome transfer (MMCT), repressed transcription of the hTERT gene. These results suggested that human chromosome 3 contains a regulatory factor(s) involved in the repression of hTERT. To further localize this putative hTERT repressor(s), we have developed a unique experimental approach by introducing various truncated chromosome 3 regions produced by a novel chromosomal engineering technology into the renal cell carcinoma cell line (RCC23 cells). These cells autonomously express ectopic hTERT (exohTERT) promoted by a retroviral LTR promoter in order to permit cellular division after repression of endogenous hTERT. We found a telomerase repressor region located within a 7-Mb interval on chromosome 3p21.3. These results provide important information regarding hTERT regulation and a unique method to identify hTERT repressor elements.
机译:端粒酶是一种合成端粒DNA的核糖核蛋白酶。通过异常上调/表达其催化亚基hTERT来重新激活端粒酶活性是人类肿瘤发生的主要途径。但是,控制hTERT表达的调节机制在很大程度上是未知的。以前,我们和其他人已经证明,通过微细胞介导的染色体转移(MMCT)引入人类3号染色体,可以抑制hTERT基因的转录。这些结果表明,人染色体3包含与hTERT的抑制有关的调节因子。为了进一步定位这种假定的hTERT阻遏物,我们已经开发了一种独特的实验方法,将由新型染色体工程技术产生的各种截短的3号染色体区域引入到肾癌细胞系(RCC23细胞)中。这些细胞自主表达由逆转录病毒LTR启动子促进的异位hTERT(exohTERT),以便在抑制内源性hTERT后允许细胞分裂。我们在染色体3p21.3上的7 Mb间隔内发现了一个端粒酶阻遏物区域。这些结果提供了有关hTERT调控的重要信息以及鉴定hTERT阻遏物元件的独特方法。

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