利用染色体工程定位人类染色体3p21.3上的hTERT抑制子区域。

Q4 Biochemistry, Genetics and Molecular Biology
Satoshi Abe, Hiromi Tanaka, Tomomi Notsu, Shin-Ichi Horike, Chikako Fujisaki, Dong-Lai Qi, Takahito Ohhira, David Gilley, Mitsuo Oshimura, Hiroyuki Kugoh
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引用次数: 14

摘要

端粒酶是一种合成端粒DNA的核糖核蛋白酶。端粒酶催化亚基hTERT的异常上调/表达对端粒酶活性的再激活是人类肿瘤发生的主要途径。然而,控制hTERT表达的调控机制在很大程度上是未知的。之前,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,抑制了hTERT基因的转录。这些结果表明,人类3号染色体含有一个参与抑制hTERT的调节因子。为了进一步定位这种假定的hTERT抑制因子,我们开发了一种独特的实验方法,将一种新的染色体工程技术产生的各种截断的3号染色体区域引入肾细胞癌细胞系(RCC23细胞)。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),从而在内源性hTERT被抑制后允许细胞分裂。我们在染色体3p21.3上发现了一个端粒酶抑制区,位于7 mb的间隔内。这些结果提供了有关hTERT调控的重要信息和鉴定hTERT抑制因子的独特方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
Genome Integrity
Genome Integrity Biochemistry, Genetics and Molecular Biology-Genetics
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