The Salk Institute for Biological Studies, Molecular and Cellular Biology Department, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
DNA Repair (Amst). 2013 Mar 1;12(3):238-45. doi: 10.1016/j.dnarep.2012.12.008. Epub 2013 Jan 21.
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.
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。