How Shelterin Solves the Telomere End-Protection Problem

被引:103
作者
de Lange, T. [1 ]
机构
[1] Rockefeller Univ, Lab Cell Biol & Genet, New York, NY 10065 USA
来源
NUCLEAR ORGANIZATION AND FUNCTION | 2010年 / 75卷
基金
美国国家卫生研究院;
关键词
DNA-DAMAGE RESPONSE; HOMOLOGOUS RECOMBINATION; POLY(ADP-RIBOSE) POLYMERASE; MAMMALIAN TELOMERES; BINDING PROTEIN; DYSFUNCTIONAL TELOMERES; LENGTH REGULATOR; BREAK REPAIR; HUMAN RAP1; TRF2;
D O I
10.1101/sqb.2010.75.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The symphony of the human genome concludes with a long Gregorian chant of TTAGGG repeats. This monotonous coda represents one of the most complex problems in chromosome biology: the question of how cells distinguish their natural chromosome ends from double-strand breaks elsewhere in the genome. McClintock's classic finding of chromosome breakage-fusion-bridge cycles, first reported by her at one of the early Cold Spring Harbor Laboratory Symposia (the ninth), served as a prelude to this question. The 75th Cold Spring Harbor Laboratory Symposium marks the completion of a series of mouse gene deletion experiments that revealed DNA-damage-response pathways that threaten chromosome ends and how the components of the telomeric shelterin complex prevent activation of these pathways.
引用
收藏
页码:167 / 177
页数:11
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