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首页> 外文期刊>Plant Disease >Repair characteristics and time-dependent effects in response to heavy-ion beam irradiation in Saccharomyces cerevisiae: a comparison with X-ray irradiation
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Repair characteristics and time-dependent effects in response to heavy-ion beam irradiation in Saccharomyces cerevisiae: a comparison with X-ray irradiation

机译:响应酵母菌酿酒酵母中重离子束照射的修复特性和时间依赖性效应:与X射线照射的比较

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Heavy-ion beam (HIB) irradiation has been widely used in microbial mutation breeding. However, a global cellular response to such radiation remains mostly uncharacterised. In this study, we used transcriptomics to analyse the damage repair response in Saccharomyces cerevisiae following a semi-lethal HIB irradiation (80 Gy), which induced a significant number of DNA double-strand breaks. Our analysis of differentially expressed genes (DEGs) from 50 to 150 min post-irradiation revealed that upregulated genes were significantly enriched for gene ontology and Kyoto encyclopaedia of genes and genomes terms related to damage repair response. Based on the number of DEGs, their annotation, and their relative expression, we established that the peak of the damage repair response occurred 75 min post-irradiation. Moreover, we exploited the data from our recent study on X-ray irradiation-induced repair to compare the transcriptional patterns induced by semi-lethal HIB and X-ray irradiations. Although these two radiations have different properties, we found a significant overlap (> 50%) for the DEGs associated with five typical DNA repair pathways and, in both cases, identified homologous recombination repair (HRR) as the predominant repair pathway. Nevertheless, when we compared the relative enrichment of the five DNA repair pathways at the key time point of the repair process, we found that the relative enrichment of HRR was higher after HIB irradiation than after X-ray irradiation. Additionally, the peak stage of HRR following HIB irradiation was ahead of that following X-ray irradiation. Since mutations occur during the DNA repair process, uncovering detailed repair characteristics should further the understanding of the associated mutagenesis features.
机译:重离子束(HIB)辐射已广泛用于微生物突变繁殖。然而,对这种辐射的全局细胞响应仍然大多是无论如何。在这项研究中,我们使用转录组织在半致死的Hib辐照(80Gy)之后分析酿酒酵母酿酒酵母的损伤修复响应,其诱导大量DNA双链断裂。我们对50至150分钟的差异表达基因(DEGS)的分析显示,对于基因本体和京都的基因和基因组术语与损伤修复反应有关的基因组织,显着富集了上调基因。基于DEG的数量,它们的注释和相对表达,我们确立了损伤修复反应的峰值发生在辐照后75分钟。此外,我们从我们最近的X射线照射诱导的修复研究中利用了数据,以比较半致死的HIB和X射线照射所引起的转录模式。虽然这两种辐射具有不同的性质,但我们发现与五种典型的DNA修复途径相关的DEG的显着重叠(> 50%),并且在这两种情况下,鉴定了同源重组修复(HRR)作为主要的修复途径。然而,当我们在修复过程的关键时间点进行比较五个DNA修复途径的相对浓缩时,我们发现HIB辐照后HRR的相对富集高于X射线照射后更高。另外,在X射线照射之后,HIB辐射后的HRR的峰阶段提前。由于在DNA修复过程中发生突变,因此揭示详细的修复特性应该进一步了解相关的诱变特征。

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