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Telomeric and extra-telomeric roles for telomerase and the telomere-binding proteins.

机译:端粒酶和端粒结合蛋白的端粒作用和端粒外作用。

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摘要

Mammalian telomeres are formed by tandem repeats of the TTAGGG sequence, which are progressively lost with each round of cell division. Telomere protection requires a minimal length of TTAGGG repeats to allow the binding of shelterin, which prevents the activation of a DNA damage response (DDR) at chromosome ends. Telomere elongation is carried out by telomerase. Telomerase can also act as a transcriptional modulator of the Wnt-beta-catenin signalling pathway and has RNA-dependent RNA polymerase activity. Dysfunctional telomeres can lead to either cancer or ageing pathologies depending on the integrity of the DDR. This Review discusses the role of telomeric proteins in cancer and ageing through modulating telomere length and protection, as well as regulating gene expression by binding to non-telomeric sites.
机译:哺乳动物端粒是由TTAGGG序列的串联重复序列形成的,随着细胞分裂的每一轮逐渐丢失。端粒保护需要最短的TTAGGG重复序列长度,以允许伞菌蛋白结合,从而阻止了染色体末端DNA损伤反应(DDR)的激活。端粒延长是通过端粒酶进行的。端粒酶还可以充当Wnt-β-catenin信号通路的转录调节剂,并具有RNA依赖性RNA聚合酶活性。功能失调的端粒取决于DDR的完整性,可导致癌症或衰老。这篇综述讨论了端粒蛋白在癌症和衰老中的作用,其通过调节端粒的长度和保护,以及通过与非端粒位点的结合来调节基因表达。

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