Moskaleva Elizaveta Yu, Glukhov Alexander I, Zhirnik Alexander S, Vysotskaya Olga V, Vorobiova Svetlana A
Kurchatov complex for NBICS Sciences and Nature-like Technologies, National Research Center "Kurchatov Institute", Moscow, 123182, Russia. ARRAY(0x63c0e4a83948).
Department of Biological Chemistry, I. M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, 119048, Russia.
Biochemistry (Mosc). 2025 Jun;90(6):700-724. doi: 10.1134/S0006297925600814.
Telomere biology still remains a topic of interest in life sciences. Analysis of several thousand clinical samples from healthy individuals performed in recent years has shown that the telomere length (TL) in peripheral blood leukocytes correlates with the TL in cells of internal organ and reflects their condition. TL decreases under the influence of damaging factors and can serve as an indicator of health status. The telomere shortening leads to the cell proliferation arrest and is considered as a marker of replicative aging of proliferating cells. A decrease in the TL in peripheral blood leukocytes is viewed as an indicator of organism aging. Recent studies have allowed to formulate the concept on the role of the CST-polymerase α/primase in the C-strand fill in after completion of 3'G overhang synthesis by telomerase during telomere replication. The discovery of the telomeric RNA (TERRA) and its role in the regulation of telomerase activity (TA) and alternative lengthening of telomeres, as well as the possibility of TERRA translation, has provided evidence of the complex epigenetic regulation of the TL maintenance. Analysis of the published data indicates that telomeres are dynamic structures, whose length undergoes significant changes under the influence of damaging factors. TL is determined not only by the chronological age, but also by the exposure to the exogenous and endogenous deleterious factors during the lifetime. A decrease in the TL due to inherited mutations in the genes coding for proteins involved in the telomere structure formation and telomere replication (primarily, proteins of the shelterin and CST complexes and telomerase) has been found in a number of hereditary diseases - telomeropathies. The assessment of TL and TA is of great importance for the diagnostics of telomeropathies and can be useful in the diagnostics of cancer. Analysis of TL can be used for monitoring the health status (e.g., in the case of exposure to ionizing radiation and space flight factors), as well as predicting individual's sensitivity to the action of various damaging agents. The application of modern advancement in genetic technologies in the analysis of TL and TA makes it available for the use in clinical and epidemiological studies, diagnostics of telomeropathies, and monitoring of astronauts' health.
端粒生物学仍然是生命科学中一个备受关注的话题。近年来对数千份来自健康个体的临床样本进行的分析表明,外周血白细胞中的端粒长度(TL)与内脏器官细胞中的TL相关,并反映其状况。TL在损伤因素的影响下会缩短,可作为健康状况的指标。端粒缩短会导致细胞增殖停滞,被认为是增殖细胞复制性衰老的标志物。外周血白细胞中TL的降低被视为机体衰老的指标。最近的研究使得人们能够阐述CST-聚合酶α/引发酶在端粒复制过程中端粒酶完成3'G悬突合成后填充C链中的作用这一概念。端粒RNA(TERRA)的发现及其在端粒酶活性(TA)调节和端粒替代延长中的作用,以及TERRA翻译的可能性,为TL维持的复杂表观遗传调控提供了证据。对已发表数据的分析表明,端粒是动态结构,其长度在损伤因素的影响下会发生显著变化。TL不仅由实际年龄决定,还受到一生中接触外源性和内源性有害因素的影响。在许多遗传性疾病——端粒病中,已发现由于编码参与端粒结构形成和端粒复制的蛋白质(主要是保护素和CST复合物的蛋白质以及端粒酶)的基因发生遗传突变而导致TL降低。TL和TA的评估对于端粒病的诊断非常重要,并且在癌症诊断中可能有用。TL分析可用于监测健康状况(例如,在接触电离辐射和太空飞行因素的情况下),以及预测个体对各种损伤因子作用的敏感性。在TL和TA分析中应用现代遗传技术的进展使其可用于临床和流行病学研究、端粒病的诊断以及宇航员健康监测。