Influence of genetic polymorphisms of Hg metabolism and DNA repair on the frequencies of micronuclei, nucleoplasmic bridges, and nuclear buds in communities living in gold mining areas

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lyda Espitia-Pérez , Hugo Brango , Ana Peñata-Taborda , Claudia Galeano-Páez , Manolo Jaramillo-García , Pedro Espitia-Pérez , Karina Pastor–Sierra , Osnamir Bru-Cordero , Luz Stella Hoyos-Giraldo , Ingrid Reyes-Carvajal , Diana Saavedra-Trujillo , Dina Ricardo-Caldera , Andrés Coneo–Pretelt
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引用次数: 0

Abstract

Fishing communities living near gold mining areas are at increased risk of mercury (Hg) exposure via bioaccumulation of methylmercury (MeHg) in fish. This exposure has been linked to health effects that may be triggered by genotoxic events. Genetic polymorphisms play a role in the risk associated with Hg exposure. This study evaluated the effect of single nucleotide polymorphisms (SNPs) in metabolic and DNA repair genes on genetic instability and total hair Hg (T-Hg) levels in 78 individuals from "La Mojana" in northern Colombia and 34 individuals from a reference area. Genetic instability was assessed by the frequency of micronuclei (MNBN), nuclear buds (NBUDS), and nucleoplasmic bridges (NPB). We used a Poisson regression to assess the influence of SNPs on T-Hg levels and genetic instability, and a Bayesian regression to examine the interaction between Hg detoxification and DNA repair. Among exposed individuals, carriers of XRCC1Arg399Gln had a significantly higher frequency of MNBN. Conversely, the XRCC1Arg194Trp and OGG1Ser326Cys polymorphisms were associated with lower frequencies of MNBN. XRCC1Arg399Gln, XRCC1Arg280His, and GSTM1Null carriers showed lower NPB frequencies. Our results also indicated that individuals with the GSTM1Null and GSTT1null polymorphisms had a 1.6-fold risk for higher T-Hg levels. The Bayesian model showed increased MNBN frequencies in carriers of the GSTM1Null polymorphism in combination with XRCC1Arg399Gln and increased NBUDS frequencies in the GSTM1Null carriers with the XRCC3Thr241Met and OGG1Ser326Cys alleles. The GSTM1+ variant was found to be a protective factor in individuals carrying OGG1Ser326Cys (MNBN) and XRCC1Arg280His (NPB); the GSTT1+ polymorphism combined with XRCCArg194Trp also modulated lower MNBN frequencies, while GSTT1+ carriers with the XRCC1Arg399Gln allele showed lower NPB frequencies. Consistent with GSTM1, GSTT1Null carriers with XRCC3Thr241Met showed increased NBUDS frequency. With the rise of gold mining activities, these approaches are vital to identify and safeguard populations vulnerable to Hg's toxic effects.

汞代谢和 DNA 修复的遗传多态性对金矿开采区居民微核、核质桥和核芽频率的影响
生活在金矿开采区附近的渔业社区,通过鱼类体内甲基汞(MeHg)的生物累积,接触汞(Hg)的风险增加。这种接触与健康影响有关,而健康影响可能是由基因毒性事件引发的。基因多态性在与汞接触相关的风险中发挥着作用。本研究评估了代谢基因和 DNA 修复基因中的单核苷酸多态性(SNPs)对哥伦比亚北部 "La Mojana "地区 78 名个体和参考地区 34 名个体的遗传不稳定性和毛发总汞含量(T-Hg)的影响。遗传不稳定性通过微核(MNBN)、核芽(NBUDS)和核质桥(NPB)的频率进行评估。我们采用泊松回归法评估 SNPs 对 T-Hg 水平和遗传不稳定性的影响,并采用贝叶斯回归法研究汞解毒与 DNA 修复之间的相互作用。在暴露个体中,XRCC1Arg399Gln携带者的MNBN频率明显较高。相反,XRCC1Arg194Trp 和 OGG1Ser326Cys 多态性与较低的 MNBN 频率相关。XRCC1Arg399Gln、XRCC1Arg280His 和 GSTM1Null 携带者的 NPB 频率较低。我们的研究结果还表明,GSTM1Null 和 GSTT1null 多态性携带者的 T-Hg 水平较高的风险是正常人的 1.6 倍。贝叶斯模型显示,GSTM1Null 多态性与 XRCC1Arg399Gln 组合的携带者的 MNBN 频率增加,GSTM1Null 与 XRCC3Thr241Met 和 OGG1Ser326Cys 等位基因组合的携带者的 NBUDS 频率增加。在携带 OGG1Ser326Cys(MNBN)和 XRCC1Arg280His(NPB)的个体中,GSTM1+变异是一个保护因素;GSTT1+多态性与 XRCCArg194Trp 结合也会调节较低的 MNBN 频率,而带有 XRCC1Arg399Gln 等位基因的 GSTT1+ 携带者则表现出较低的 NPB 频率。与 GSTM1 相一致,带有 XRCC3Thr241Met 的 GSTT1Null 携带者的 NBUDS 频率增加。随着金矿开采活动的增加,这些方法对于识别和保护易受汞毒性影响的人群至关重要。
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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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