共 110 条
How Shelterin Solves the Telomere End-Protection Problem
被引:103
作者:

de Lange, T.
论文数: 0 引用数: 0
h-index: 0
机构:
Rockefeller Univ, Lab Cell Biol & Genet, New York, NY 10065 USA Rockefeller Univ, Lab Cell Biol & Genet, New York, NY 10065 USA
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.
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页码:167 / 177
页数:11
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共 110 条
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