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5' C-丰富的端粒突出端是端粒快速截短事件的结果。

5' C-rich telomeric overhangs are an outcome of rapid telomere truncation events.

机构信息

The Salk Institute for Biological Studies, Molecular and Cellular Biology Department, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

DNA Repair (Amst). 2013 Mar 1;12(3):238-45. doi: 10.1016/j.dnarep.2012.12.008. Epub 2013 Jan 21.

Abstract

A subset of human tumors ensures indefinite telomere length maintenance by activating a telomerase-independent mechanism known as Alternative Lengthening of Telomeres (ALT). Most tumor cells of ALT origin share a constellation of unique characteristics, which include large stores of extra-chromosomal telomeric material, chronic telomere dysfunction and a peculiar enrichment in chromosome ends with 5' C-rich overhangs. Here we demonstrate that acute telomere de-protection and the subsequent DNA damage signal are not sufficient to facilitate formation of 5' C-overhangs at the chromosome end. Rather chromosome ends bearing 5' C-overhangs are a by-product of rapid cleavage events, processing of which occurs independently of the DNA damage response and is partly mediated through the XRCC3 endonuclease.

摘要

人类肿瘤的一个亚群通过激活一种称为端粒酶非依赖性机制(ALT)的端粒长度维持机制来确保端粒的无限延长。大多数 ALT 来源的肿瘤细胞具有一系列独特的特征,包括大量额外的染色体端粒物质、慢性端粒功能障碍和染色体末端富含 5' C 丰富的突出物。在这里,我们证明急性端粒去保护和随后的 DNA 损伤信号不足以促进染色体末端 5' C 突出物的形成。相反,带有 5' C 突出物的染色体末端是快速切割事件的产物,其加工过程独立于 DNA 损伤反应,部分通过 XRCC3 内切酶介导。

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