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首页> 外文期刊>Health Physics: Official Journal of the Health Physics Society >Gene expression analysis in mayak workers with prolonged occupational radiation exposure
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Gene expression analysis in mayak workers with prolonged occupational radiation exposure

机译:基因表达分析在克工人长期的职业辐射照射

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The authors evaluated gene expression in the peripheral blood in relation to occupational exposure in Mayak workers to find out about the existence of a permanent post exposure signature. Workers were exposed to combined incorporated Pu and external gamma rays (n = 82) or to external gamma rays only (n = 18), and 50 unexposed individuals served as controls. Peripheral blood was taken from workers older than 70 y. RNA was isolated, converted into cDNA, and stored at -20°C. A two-stage study design was performed focusing on examinations on the transcriptional (mRNA) and post-transcriptional level (microRNA). In the first stage, 40 samples were identified for screening purposes and selection of candidate genes. For examinations on the transcriptional level, whole genome microarrays and qRT-PCR were employed on the post-transcriptional level (667 microRNAs). Candidate genes were assessed by (1) introducing a twofold difference in gene expression over the reference group and (2) showing a significant p-value using the Kruskal-Wallis test. From 42,545 transcripts of the whole genome microarray, 376 candidate genes (80 up-regulated and 296 down-regulated relative to the reference group) were selected. Expression of almost all of these genes (70-98%) appeared significantly associated with internal Pu and to a lesser extent were associated with external gamma-ray exposure (2-30%). Associations in the same direction were found for 45 microRNAs. Although both exposures led to modulations of different gene sets in different directions, the authors could detect no differences in gene set enrichment analysis.
机译:作者评估基因表达的外周血和职业的关系暴露在克员工了解存在一个永久接触后签名。工人被暴露于合并Pu相结合和外部的伽马射线(n = 82)或外部伽马射线只(n = 18), 50个未曝光个人担任控制。来自工人超过70 y。RNA是什么孤立的,转换成cDNA、和存储-20°C。专注于考试转录(信使rna)和转录后水平(微)。在第一阶段,40个样本用于筛选和选择的候选人基因。水平,全基因组芯片和存在在转录后水平(667小分子核糖核酸)。引入两个差异基因参照群体和表达(2)显示重要的假定值使用克鲁斯卡尔-沃利斯测试。整个基因组芯片,376个候选基因(296年80上调和下调相对参照组)。几乎所有这些基因(70 - 98%)出现了与内部Pu和显著相关一定程度上是与外部联系在一起γ射线照射(2 - 30%)。同一方向45小分子核糖核酸中被发现。尽管风险导致的调节在不同的方向,不同的基因集作者没有发现差异基因集富集分析。

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