Bolzán Alejandro D
Laboratorio de Citogenética y Mutagénesis, Instituto Multidisciplinario de Biología Celular (IMBICE, CONICET-UNLP-CICPBA), calle 526 y Camino General Belgrano, La Plata, Buenos Aires B1906APO, Argentina; Universidad Nacional de La Plata, Facultad de Ciencias Naturales y Museo, calle 60 y 122, La Plata, Buenos Aires, Argentina.
Mutat Res Rev Mutat Res. 2024 Jul-Dec;794:108507. doi: 10.1016/j.mrrev.2024.108507. Epub 2024 May 25.
Given that telomeres play a fundamental role in maintaining genomic stability, the study of the chromosomal aberrations involving telomeric sequences is a topic of considerable research interest. In recent years, the scoring of these types of aberrations has been used in vertebrate cells, particularly human cells, to evaluate the effects of genotoxic agents on telomeres and the involvement of telomeric sequences on chromosomal aberrations. Currently, chromosomal aberrations involving telomeric sequences are evaluated in peripheral blood lymphocytes or immortalized cell lines, using telomere or telomere plus centromere fluorescence in situ hybridization (FISH) with Peptide Nucleic Acid (PNA) probes (PNA-FISH). The telomere PNA probe is more efficient in the detection of telomeric sequences than conventional FISH with a telomere DNA probe. In addition, the intensity of the telomeric PNA-FISH probe signal is directly correlated with the number of telomeric repeats. Therefore, use of this type of probe can identify chromosomal aberrations involving telomeres as well as determine the telomere length of the sample. There are several mistakes and inconsistencies in the literature regarding the identification of telomere aberrations, which prevent accurate scoring and data comparison between different publications concerning these types of aberrations. The aim of this review is to clarify these issues, and provide proper terminology and criteria for the identification, scoring, and analysis of telomere aberrations.
鉴于端粒在维持基因组稳定性中发挥着重要作用,对涉及端粒序列的染色体畸变的研究是一个备受关注的研究课题。近年来,这类畸变的计分已用于脊椎动物细胞,特别是人类细胞,以评估遗传毒性剂对端粒的影响以及端粒序列在染色体畸变中的作用。目前,使用端粒或端粒加着丝粒荧光原位杂交(FISH)和肽核酸(PNA)探针(PNA-FISH)在外周血淋巴细胞或永生化细胞系中评估涉及端粒序列的染色体畸变。与使用端粒DNA探针的传统FISH相比,端粒PNA探针在检测端粒序列方面更有效。此外,端粒PNA-FISH探针信号的强度与端粒重复序列的数量直接相关。因此,使用这类探针可以识别涉及端粒的染色体畸变,并确定样品的端粒长度。关于端粒畸变的识别,文献中存在一些错误和不一致之处,这妨碍了对这类畸变进行准确计分以及不同出版物之间的数据比较。本综述的目的是澄清这些问题,并为端粒畸变的识别、计分和分析提供恰当的术语和标准。