首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Polo-like Kinase 1 (Plk1) Up-regulates Telomerase Activity by Affecting Human Telomerase Reverse Transcriptase (hTERT) Stability
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Polo-like Kinase 1 (Plk1) Up-regulates Telomerase Activity by Affecting Human Telomerase Reverse Transcriptase (hTERT) Stability

机译:马球样激酶1(Plk1)通过影响人类端粒酶逆转录酶(hTERT)稳定性上调端粒酶活性。

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摘要

Maintenance of telomere is regulated by active telomerase complex, including telomerase holoenzyme and its associated proteins. The activity of telomerase is precisely controlled in cells, and its dysregulation is one of the hallmarks of cancer. The telomerase catalytic subunit human telomerase reverse transcriptase (hTERT) plays a central role for telomerase activity. In this study, we indentified that Polo-like kinase 1 (Plk1) is a novel telomerase-associated protein. Plk1 can interact with hTERT independently of its kinase activity. More importantly, we found that Plk1 is associated with active telomerase complex. In addition, we demonstrated that knockdown of Plk1 caused the reduction of telomerase activity, whereas overexpression of Plk1 increased telomerase activity. Further analysis showed that overexpression of Plk1 led to a significant increase of hTERT protein by prolonging its half-life but did not affect the level of hTERT mRNA. Furthermore, we found that Plk1 enhanced the chromatin loading of hTERT and inhibited its ubiquitination. This implied that Plk1 affected hTERT stability by inhibiting its ubiquitin-mediated degradation. Collectively, these observations suggested that Plk1 is a positive modulator of telomerase by enhancing the stability of hTERT.
机译:端粒的维持受活性端粒酶复合物(包括端粒酶全酶及其相关蛋白)的调节。端粒酶的活性在细胞中得到精确控制,其失调是癌症的标志之一。端粒酶催化亚基人端粒酶逆转录酶(hTERT)在端粒酶活性中起着核心作用。在这项研究中,我们确定了Polo样激酶1(Plk1)是一种新型的端粒酶相关蛋白。 Plk1可以独立于hTERT与其激酶活性相互作用。更重要的是,我们发现Plk1与活性端粒酶复合物相关。此外,我们证明了敲低Plk1会导致端粒酶活性降低,而Plk1的过表达会增加端粒酶活性。进一步的分析表明,Plk1的过表达通过延长其半衰期而导致hTERT蛋白的显着增加,但并不影响hTERT mRNA的水平。此外,我们发现Plk1增强了hTERT的染色质负载并抑制了其泛素化。这暗示Plk1通过抑制其泛素介导的降解影响hTERT稳定性。总体而言,这些观察结果表明,Plk1通过增强hTERT的稳定性是端粒酶的正调节剂。

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