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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >CTCF mediates the TERT enhancer-promoter interactions in lung cancer cells: Identification of a novel enhancer region involved in the regulation of TERT gene
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CTCF mediates the TERT enhancer-promoter interactions in lung cancer cells: Identification of a novel enhancer region involved in the regulation of TERT gene

机译:CTCF介导肺癌细胞中TERT增强子-启动子的相互作用:鉴定涉及TERT基因调控的新型增强子区域

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Telomerase activation is a hallmark of cancer. Although the regulation of the telomerase reverse transcriptase catalytic subunit (TERT), the rate-limiting factor for telomerase activity, has been studied intensively it remains incompletely understood. In cells devoid of telomerase activity, TERT is embedded in a region of condensed chromatin and the chromatin remodeling protein CCCTC-binding factor (CTCF) has been implicated in the inhibition of TERT expression. The importance of TERT activation for cellular immortalization and carcinogenesis is attested by the fact that the gene is expressed in more than 90% of immortal cell lines and tumors and that gain of TERT is the most frequent amplification event in early stage lung cancer. This study was designed to study the mechanisms of regulation of the TERT gene expression by the CTCF transcription factor in three human lung cancer cell lines, A427, A549 and H838. Depletion of CTCF by siRNA resulted in reduced TERT mRNA levels in two (A427 and A549) of the three cell lines. A novel enhancer element was identified approximately 4.5 kb upstream of the TERT transcription start site. Chromatin immunoprecipitation experiments revealed recruitment of CTCF to this enhancer element. Chromosome conformation capture experiments demonstrated the presence of CTCF-dependent chromatin loops between this enhancer element and the TERT proximal promoter in A427 and A549 cell lines. In summary, the results show that CTCF plays an important role in maintaining TERT expression in a subset of human lung cancer cell lines. This role may be due to CTCF-dependent enhancer-promoter interactions.
机译:端粒酶激活是癌症的标志。尽管已经深入研究了端粒酶逆转录酶催化亚基(TERT)的调控,端粒酶活性的速率限制因子,但仍不完全了解。在没有端粒酶活性的细胞中,TERT嵌入浓缩的染色质区域中,并且染色质重塑蛋白CCCTC结合因子(CTCF)与抑制TERT表达有关。 TERT激活对于细胞永生化和致癌作用的重要性由以下事实证明:该基因在90%以上的永生细胞系和肿瘤中表达,而TERT的获得是早期肺癌中最频繁的扩增事件。本研究旨在研究CTCF转录因子在三种人类肺癌细胞A427,A549和H838中调节TERT基因表达的机制。 siRNA消耗CTCF导致三种细胞系中两种(A427和A549)的TERT mRNA水平降低。在TERT转录起始位点上游约4.5 kb处发现了一个新的增强子元件。染色质免疫沉淀实验表明,CTCF募集到该增强子元件上。染色体构象捕获实验表明,在A427和A549细胞系中,该增强子元件与TERT近端启动子之间存在CTCF依赖性染色质环。总之,结果表明,CTCF在维持人肺癌细胞亚群中TERT的表达中起着重要作用。此作用可能是由于依赖CTCF的增强子-启动子相互作用。

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