LINE-1 甲基化指数与姊妹染色单体交换和染色单体畸变(而非染色体畸变)相关,而这些姊妹染色单体交换和染色单体畸变发生在一个含有钚 239 的核化学设施的人员身上

IF 0.6 4区 生物学 Q4 GENETICS & HEREDITY Russian Journal of Genetics Pub Date : 2024-05-03 DOI:10.1134/s1022795424040148
S. A. Vasilyev, E. N. Tolmacheva, E. A. Sazhenova, N. N. Sukhanova, Yu. S. Yakovleva, N. B. Torkhova, M. B. Plaksin, I. N. Lebedev
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引用次数: 0

摘要

摘要 成年个体体细胞中染色体异常的程度具有显著的个体差异,这可能部分受到遗传和表观遗传背景的影响。细胞中的表观遗传景观主要由基因组甲基化决定。本研究旨在分析全球基因组甲基化与钚工人淋巴细胞染色体异常频率之间的关系。研究分析了 40 名来自掺入了钚 239 的核化学工厂(俄罗斯塞韦尔斯克)的男性工人和 49 名未受到电离辐射职业暴露的健康男性志愿者的淋巴细胞中染色体畸变、微核、2、7、8、12、X 和 Y 染色体非整倍体以及姐妹染色单体交换的频率。长穿插核元素-1(LINE-1)甲基化指数是全球基因组甲基化的一个著名标记。工人组的中心粒阴性微核(4.74 ± 2.26 vs. 3.02 ± 1.69‰)、染色体类型畸变(0.81 ± 0.79 vs. 0.44 ± 0.69%)和染色体总不连接(0.93 ± 0.43 vs. 0.50 ± 0.25%)的频率明显高于对照组(p <0.05)。工人组和对照组的 LINE-1 甲基化指数差异不大(74.93 ± 3.63 vs. 73.92 ± 4.62%)。在对照组中观察到 LINE-1 甲基化与微核频率之间存在相关性(R = -0.35,p = 0.031),而只在钚工人组中观察到 LINE-1 甲基化与染色体类型畸变(R = -0.42,p = 0.012)(但不包括染色体类型畸变)和姐妹染色单体交换(R = -0.53,p = 0.004)之间存在相关性。因此,钚暴露后的LINE-1低甲基化主要与染色体断裂(修复或修复不良)有关。
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LINE-1 Methylation Index Correlates with Sister Chromatid Exchanges and Chromatid but Not Chromosome Aberrations in Personnel from a Nuclear Chemical Facility with Incorporated Plutonium-239

Abstract

The level of chromosomal abnormalities in the somatic cells of adult individuals is characterized by significant interindividual variability, which may be partly affected by the genetic and epigenetic background. The epigenetic landscape in cells is largely determined by genome methylation. This study aimed to analyze the relationships between global genome methylation and the frequencies of chromosome abnormalities in lymphocytes of plutonium workers. The frequencies of chromosome aberrations, micronuclei, aneuploidy of chromosomes 2, 7, 8, 12, X, and Y and sister chromatid exchanges were analyzed in the lymphocytes of 40 male workers from a nuclear chemical facility (Seversk, Russia) with incorporated plutonium-239 and 49 healthy male volunteers who had no occupational exposure to ionizing radiation. The long interspersed nuclear elements-1 (LINE-1) methylation index was assessed as a well-known marker of global genome methylation. The frequencies of centromere-negative micronuclei (4.74 ± 2.26 vs. 3.02 ± 1.69‰), chromosome-type aberrations (0.81 ± 0.79 vs. 0.44 ± 0.69%), and total chromosome non-disjunction (0.93 ± 0.43 vs. 0.50 ± 0.25%) were significantly higher in the group of workers than in controls (p < 0.05). The LINE-1 methylation index did not differ significantly between the worker and control groups (74.93 ± 3.63 vs. 73.92 ± 4.62%). Correlations between LINE-1 methylation and the frequency of micronuclei (R = –0.35, p = 0.031) were observed in the control group, whereas correlations of LINE-1 methylation with chromatid-type aberrations (R = –0.42, p = 0.012) (but not chromosome-type aberrations) and with sister chromatid exchanges (R = –0.53, p = 0.004) were observed only in the group of plutonium workers. Thus, LINE-1 hypomethylation after plutonium exposure is associated mainly with chromatid breaks, either repaired or misrepaired.

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来源期刊
Russian Journal of Genetics
Russian Journal of Genetics 生物-遗传学
CiteScore
1.00
自引率
33.30%
发文量
126
审稿时长
1 months
期刊介绍: Russian Journal of Genetics is a journal intended to make significant contribution to the development of genetics. The journal publishes reviews and experimental papers in the areas of theoretical and applied genetics. It presents fundamental research on genetic processes at molecular, cell, organism, and population levels, including problems of the conservation and rational management of genetic resources and the functional genomics, evolutionary genomics and medical genetics.
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