Yu Hyeon Jong, Byun Yoon Hwan, Park Chul-Kee
Department of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Department of Neurosurgery, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea.
Comput Struct Biotechnol J. 2024 Apr 10;23:1489-1498. doi: 10.1016/j.csbj.2024.04.011. eCollection 2024 Dec.
Telomeres are located at the ends of chromosomes and have specific sequences with a distinctive structure that safeguards genes. They possess capping structures that protect chromosome ends from fusion events and ensure chromosome stability. Telomeres shorten in length during each cycle of cell division. When this length reaches a certain threshold, it can lead to genomic instability, thus being implicated in various diseases, including cancer and neurodegenerative disorders. The possibility of telomeres serving as a biomarker for aging and age-related disease is being explored, and their significance is still under study. This is because post-mitotic cells, which are mature cells that do not undergo mitosis, do not experience telomere shortening due to age. Instead, other causes, for example, exposure to oxidative stress, can directly damage the telomeres, causing genomic instability. Nonetheless, a general agreement has been established that measuring telomere length offers valuable insights and forms a crucial foundation for analyzing gene expression and epigenetic data. Numerous approaches have been developed to accurately measure telomere lengths. In this review, we summarize various methods and their advantages and limitations for assessing telomere length.
端粒位于染色体末端,具有特定序列和独特结构,可保护基因。它们拥有帽状结构,能保护染色体末端不发生融合事件并确保染色体稳定性。在细胞分裂的每个周期中,端粒长度都会缩短。当这个长度达到一定阈值时,会导致基因组不稳定,进而引发包括癌症和神经退行性疾病在内的各种疾病。目前正在探索端粒作为衰老和与年龄相关疾病生物标志物的可能性,其意义仍在研究中。这是因为不再进行有丝分裂的成熟细胞(即后有丝分裂细胞)不会因年龄增长而出现端粒缩短。相反,其他因素,例如暴露于氧化应激下,可直接损伤端粒,导致基因组不稳定。尽管如此,人们已达成普遍共识,即测量端粒长度能提供有价值的见解,并为分析基因表达和表观遗传数据奠定关键基础。现已开发出多种方法来精确测量端粒长度。在本综述中,我们总结了评估端粒长度的各种方法及其优缺点。