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首页> 外文期刊>Molecular biology of the cell >An InCytes from MBC Selection: Telomerase Reverse Transcriptase Is Required for the Localization of Telomerase RNA to Cajal Bodies and Telomeres in Human Cancer Cells
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An InCytes from MBC Selection: Telomerase Reverse Transcriptase Is Required for the Localization of Telomerase RNA to Cajal Bodies and Telomeres in Human Cancer Cells

机译:从MBC选择中获得的InCytes:端粒酶逆转录酶是将端粒酶RNA定位到人类癌细胞中的Cajal体和端粒所必需的

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Telomere maintenance by telomerase is critical for the unlimited division potential of most human cancer cells. The two essential components of human telomerase, telomerase RNA (hTR) and telomerase reverse transcriptase (hTERT), are recruited from distinct subnuclear sites to telomeres during S phase. Throughout the remainder of the cell cycle hTR is found primarily in Cajal bodies. The localization of hTR to Cajal bodies and telomeres is specific to cancer cells where telomerase is active and is not observed in primary cells. Here we show that the trafficking of hTR to both telomeres and Cajal bodies depends on hTERT. RNA interference–mediated depletion of hTERT in cancer cells leads to loss of hTR from both Cajal bodies and telomeres without affecting hTR levels. In addition, expression of hTERT in telomerase-negative cells (including primary and ALT cancer cell lines) induces hTR to localize to both sites. Factors that did not stimulate hTR localization in our experiments include increased hTR RNA levels and Cajal body numbers, and expression of SV40 large T antigen and oncogenic Ras. Our findings suggest that the trafficking of telomerase to Cajal bodies and telomeres in cancer cells correlates with and depends on the assembly of the enzyme.
机译:端粒酶维持端粒对于大多数人类癌细胞的无限分裂潜力至关重要。人端粒酶的两个基本成分,端粒酶RNA(hTR)和端粒酶逆转录酶(hTERT),在S期从不同的亚核位点被募集到端粒中。在整个细胞周期的其余时间内,hTR主要存在于Cajal体中。 hTR在Cajal体和端粒中的定位是特定于癌细胞的,端粒酶是活跃的,在原代细胞中未观察到。在这里,我们表明,hTR向端粒和Cajal体的运输均取决于hTERT。 RNA干扰介导的癌细胞中hTERT的消耗导致cajal体和端粒的hTR丧失,而不会影响hTR水平。此外,hTERT在端粒酶阴性细胞(包括原发性和ALT癌细胞系)中的表达诱导hTR定位于两个位点。在我们的实验中,不能刺激hTR定位的因素包括hTR RNA水平和Cajal体数增加,以及SV40大T抗原和致癌Ras的表达。我们的发现表明,端粒酶向癌细胞中Cajal体和端粒的运输与酶的组装有关并取决于其组装。

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