Kappei Dennis, Londoño-Vallejo J Arturo
Telomeres & Cancer Laboratory, UMR7147, Institut Curie-CNRS-UPMC, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
Mech Ageing Dev. 2008 Jan-Feb;129(1-2):17-26. doi: 10.1016/j.mad.2007.10.009. Epub 2007 Oct 30.
Telomere shortening accompanies human aging, and premature aging syndromes are often associated with short telomeres. These two observations are central to the hypothesis that telomere length directly influences longevity. If true, genetically determined mechanisms of telomere length homeostasis should significantly contribute to variations of longevity in the human population. On the other hand, telomere shortening is also observed in the course of many aging-associated disorders but determining whether it is a cause or a consequence is not an easy task. Here, we review the most relevant experimental and descriptive data relating telomere length, as a quantitative trait, to aging and longevity.
端粒缩短伴随着人类衰老,早衰综合征常与短端粒相关。这两个观察结果是端粒长度直接影响寿命这一假说的核心。如果这一假说成立,由基因决定的端粒长度稳态机制应在很大程度上导致人类群体寿命的差异。另一方面,在许多与衰老相关的疾病过程中也观察到了端粒缩短,但要确定它是病因还是结果并非易事。在此,我们综述了将端粒长度作为一种数量性状与衰老和寿命相关的最相关实验和描述性数据。