University of Kent, School of Biosciences, Giles Lane, Canterbury, Kent, CT2-7NJ, UK.
Department of Child Health, East Kent Hospitals University Foundation NHS Trust, William Harvey Hospital, Ashford, Kent, TN24-0LZ, UK.
Cells. 2019 Jan 19;8(1):73. doi: 10.3390/cells8010073.
Telomeres are nucleoprotein structures that cap the end of each chromosome arm and function to maintain genome stability. The length of telomeres is known to shorten with each cell division and it is well-established that telomere attrition is related to replicative capacity in vitro. Moreover, telomere loss is also correlated with the process of aging in vivo. In this review, we discuss the mechanisms that lead to telomere shortening and summarise telomere homeostasis in humans throughout a lifetime. In addition, we discuss the available evidence that shows that telomere shortening is related to human aging and the onset of age-related disease.
端粒是一种核蛋白结构,位于每条染色体臂的末端,其功能是维持基因组的稳定性。已知端粒的长度会随着每个细胞分裂而缩短,并且已经确立端粒损耗与体外的复制能力有关。此外,端粒的丢失也与体内衰老过程有关。在这篇综述中,我们讨论了导致端粒缩短的机制,并总结了人类在整个生命周期中端粒的动态平衡。此外,我们还讨论了现有的证据,表明端粒缩短与人类衰老和与年龄相关的疾病的发生有关。