School of Biological Sciences, University of East Anglia, Norwich Research Park, Norfolk, UK.
Aging Cell. 2011 Dec;10(6):913-21. doi: 10.1111/j.1474-9726.2011.00741.x. Epub 2011 Sep 28.
Males and females often age at different rates resulting in longevity 'gender gaps', where one sex outlives the other. Why the sexes have different lifespans is an age-old question, still fiercely debated today. One cellular process related to lifespan, which is known to differ according to sex, is the rate at which the protective telomere chromosome caps are lost. In humans, men have shorter lifespans and greater telomere shortening. This has led to speculation in the medical literature that sex-specific telomere shortening is one cause of sex-specific mortality. However, telomere shortening may be a cause for and/or a consequence of the processes that govern survival, and to infer general principles from single-taxon studies may be misleading. Here, we review recent work on telomeres in a variety of animal taxa, including those with reverse sexual lifespan dimorphism (i.e., where males live longer), to establish whether sex-specific survival is generally associated with sex differences in telomere dynamics. By doing this, we attempt to tease apart the potential underlying causes for sex differences in telomere lengths in humans and highlight targets for future research across all taxa.
男性和女性的衰老速度往往不同,导致长寿“性别差距”,即一种性别比另一种性别活得更久。为什么性别会有不同的寿命是一个古老的问题,至今仍在激烈争论。与寿命相关的一个细胞过程,即保护性端粒染色体帽丢失的速度,已知根据性别而有所不同。在人类中,男性的寿命更短,端粒缩短更多。这导致医学文献中推测,性别特异性端粒缩短是性别特异性死亡率的一个原因。然而,端粒缩短可能是决定生存过程的原因和/或结果,并且从单一分类群研究中推断一般原则可能会产生误导。在这里,我们回顾了最近在各种动物分类群中端粒的研究工作,包括那些具有相反性寿命二态性(即,男性寿命更长)的分类群,以确定性别特异性存活是否通常与端粒动力学中的性别差异相关。通过这样做,我们试图梳理出人类中端粒长度存在性别差异的潜在根本原因,并强调所有分类群中未来研究的目标。