Telomere length profiles in humans -: All ends are not equal

被引:38
作者
Gilson, Eric
Londono-Vallejo, Arturo
机构
[1] Ecole Normale Super Lyon, Fac Med, Mol Cell Biol Lab, Lyon, France
[2] UPMC, CNRS, Inst Curie, Telomere & Canc Lab, Paris, France
关键词
telomere; telomerase; length regulation; counting mechanism; length polymorphism; cis-acting factors;
D O I
10.4161/cc.6.20.4798
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Telomere length is an important parameter of telomere function since it determines number of aspects controlling chromosome stability and cell division. Since telomeres shorten with age in humans and premature aging syndromes are often associated with the presence of short telomeres, it has been proposed that telomere length is also an important parameter for organismal aging. How mean telomere lengths are determined in humans remains puzzling, but it is clear that genetic and epigenetic factors appear to be of great importance. Experimental evidence obtained from many different organisms has provided the basis for a widely accepted counting mechanism based on a negative feedback loop for telomerase activity at the level of individual telomeres. In addition, recent studies in both normal and pathological contexts point to the existence of chromosome-specific mechanisms of telomere length regulation determining a telomere length profile, which is inherited and maintained throughout life. In this review, we recapitulate the available data, propose a synthetic view of telomere length control mechanisms in humans and suggest new approaches to test current hypotheses.
引用
收藏
页码:2486 / 2494
页数:9
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