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Insights into Cdc13 dependent telomere length regulation

机译:洞察Cdc13依赖的端粒长度调节

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摘要

Cdc13 is a single stranded telomere binding protein that specifically localizes to the telomere ends of budding yeasts and is essential for cell viability. It caps the ends of chromosomes thus preventing chromosome end-to-end fusions and exonucleolytic degradation, events that could lead to genomic instability and senescence, the hallmark of aging. Cdc13 is also involved in telomere length regulation by recruiting or preventing access of telomerase to the telomeric overhang. Recruitment of telomerase to the telomeres for G-strand extension is required for continuous cell division, while preventing its access to the telomeres through capping the chromosome ends prevents mitotic events that could lead to cell immortality, the hall mark of carcinogenesis. Cdc13 and its putative homologues human CTC1 and POT1 are therefore key to many biological processes directly associated with life extension and cancer prevention and can be viewed as an ideal target for cancer and age related therapies.
机译:Cdc13是单链端粒结合蛋白,其特异性定位于发芽酵母的端粒末端,对于细胞活力至关重要。它覆盖了染色体的末端,从而防止了染色体的端到端融合和核酸外切降解,这些事件可能导致基因组不稳定和衰老,这是衰老的标志。 Cdc13还通过募集或阻止端粒酶进入端粒突出端来参与端粒长度调节。连续细胞分裂需要将端粒酶招募至端粒以进行G链延伸,同时通过覆盖染色体末端阻止端粒酶接近端粒可防止有丝分裂事件,这可能导致细胞永生,这是致癌作用的标志。因此,Cdc13及其推定的同源物人类CTC1和POT1是许多与寿命延长和癌症预防直接相关的生物学过程的关键,可以被视为癌症和年龄相关疗法的理想靶标。

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