遗传变异对NADPH氧化酶活性的影响:一项广泛的基因型-表型评估。

IF 3.6 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Tana Takacova, Markus Anton Schirmer
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引用次数: 0

摘要

简介:氧化应激与多种疾病有关,NADPH氧化酶复合物(NOX)是活性氧(ROS)的重要来源。将遗传多态性与酶活性联系起来的研究产生了相互矛盾的结果。方法:我们的目标是建立一个强大的方案,在高度标准化的条件下评估体外NOX活性,并将这些测量结果与1000个人类基因组和HapMap项目编目的遗传多态性相关联。淋巴母细胞样细胞系(LCLs)作为模型系统,样本来自三个高加索人群的健康参与者。在290个LCL中(198个在训练组,92个在测试组),利用化学发光技术测量了12-肉豆蔻酸13-醋酸phorbol激发的氮氧化物活性,每个LCL进行了一系列多次重复测量,总共超过1500次氮氧化物活性评估。随后研究了NOX活性与NOX亚基基因CYBA、CYBB、NCF1、NCF2和NCF4的单核苷酸多态性(snp)之间的关系。结果:在639个有效多态性标记中,314个小等位基因频率≥5%,15个snp与训练集中NOX活性有统计学显著相关。然而,这15种关联在检验集中未得到证实(p均≥0.1)。将所有290个lcl作为一个单一队列进行的额外分析得出了三个关联,结论:我们的结果不支持NOX亚基共同遗传多样性对白种人受试者酶活性的可重复影响。这项研究是迄今为止关于氮氧化物基因变异与酶活性之间关系的最大评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of genetic variability on NADPH oxidase activity: An extensive genotype-phenotype assessment.

Introduction: Oxidative stress is implicated in various diseases, and the NADPH oxidase enzyme complex (NOX) is a significant source of reactive oxygen species (ROS). Research linking genetic polymorphisms to enzyme activity has produced conflicting results.

Methods: We aimed to establish a robust protocol to assess NOX activity in vitro under highly standardized conditions and correlate these measurements with genetic polymorphisms catalogued by the 1000 Human Genome and HapMap projects. Lymphoblastoid cell lines (LCLs) served as a model system with samples from healthy participants from three Caucasian populations. NOX activity stimulated by phorbol 12-myristate 13-acetate was measured using chemiluminescence in 290 LCLs (198 in a training and 92 in a test set) through a series of multiply repeated measurements per LCL comprising in total over 1,500 NOX activity assessments. The association between NOX activity and single nucleotide polymorphisms (SNPs) in the NOX subunit genes CYBA, CYBB, NCF1, NCF2, and NCF4 was subsequently examined.

Results: Out of 639 valid polymorphic markers, 314 had a minor allele frequency of ≥5%, and 15 SNPs showed a statistically significant correlation with NOX activity in the training set. However, these 15 associations were not confirmed in the test set (all p ≥ 0.1). Additional analyses treating all 290 LCLs as a single cohort yielded three associations at p < 0.01, i.e. CYBA rs1017828, NCF1 rs191081238, and NCF4 rs4821544. However, statistical significance could not be called for any of these genetic markers upon adjustment for multiple testing, regardless whether a co-dominant, dominant or recessive allelic effect was assumed.

Conclusion: Our results do not support a reproducible impact of common genetic diversity in NOX subunits on the enzyme activity in subjects of Caucasian origin. This study represents the largest evaluation concerning relationships between NOX genetic variants and enzyme activity to date.

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来源期刊
Free Radical Research
Free Radical Research 生物-生化与分子生物学
CiteScore
6.70
自引率
0.00%
发文量
47
审稿时长
3 months
期刊介绍: Free Radical Research publishes high-quality research papers, hypotheses and reviews in free radicals and other reactive species in biological, clinical, environmental and other systems; redox signalling; antioxidants, including diet-derived antioxidants and other relevant aspects of human nutrition; and oxidative damage, mechanisms and measurement.
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