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Chromatin regulation and non-coding RNAs at mammalian telomeres
被引:63
|作者:
Schoeftner, Stefan
[1
]
Blasco, Maria A.
[1
]
机构:
[1] Spanish Natl Canc Res Ctr CNIO, Mol Oncol Program, Telomeres & Telomerase Grp, Madrid 28029, Spain
关键词:
Telomeres;
Epigenetics;
TelRNA;
TERRA;
Telomeric chromatin;
Silencing;
HISTONE H3 LYSINE-9;
PLURIPOTENT STEM-CELLS;
REPEAT-CONTAINING RNA;
DNA METHYLATION;
EPIGENETIC REGULATION;
HOMOLOGOUS RECOMBINATION;
CHROMOSOMAL INSTABILITY;
SILENCED CHROMATIN;
LIFE-SPAN;
RB FAMILY;
D O I:
10.1016/j.semcdb.2009.09.015
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
In eukaryotes, terminal chromosome repeats are bound by a specialized nucleoprotein complex that controls telomere length and protects chromosome ends from DNA repair and degradation. In mammals the "shelterin" complex mediates these central functions at telomeres. In the recent years it has become evident that also the heterochromatic structure of mammalian telomeres is implicated in telomere length regulation. Impaired telomeric chromatin compaction results in a loss of telomere length control. Progressive telomere shortening affects chromatin compaction at telomeric and subtelomeric repeats and activates alternative telomere maintenance mechanisms. Dynamics of chromatin structure of telomeres during early mammalian development and nuclear reprogramming further indicates a central role of telomeric heterochromatin in organismal development. In addition, the recent discovery that telomeres are transcribed, giving rise to UUAGGG-repeat containing TelRNAs/TERRA, opens a new level of chromatin regulation at telomeres. Understanding the links between the epigenetic status of telomeres, TERRA/TelRNA and telomere homeostasis will open new avenues for our understanding of organismal development, cancer and ageing. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:186 / 193
页数:8
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