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Nucleosomes effectively shield DNA from radiation damage in living cells

机译:核体有效地保护DNA免受活细胞的辐射损伤

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Eukaryotic DNA is organized in nucleosomes, which package DNA and regulate its accessibility to transcription, replication, recombination and repair. Here, we show that in living cells nucleosomes protect DNA from high-energy radiation and reactive oxygen species. We combined sequence-based methods (ATAC-seq and BLISS) to determine the position of both nucleosomes and double strand breaks (DSBs) in the genome of nucleosome-rich malignant mesothelioma cells, and of the same cells partially depleted of nucleosomes. The results were replicated in the human MCF-7 breast carcinoma cell line. We found that, for each genomic sequence, the probability of DSB formation is directly proportional to the fraction of time it is nucleosome-free; DSBs accumulate distal from the nucleosome dyad axis. Nucleosome free regions and promoters of actively transcribed genes are more sensitive to DSB formation, and consequently to mutation. We argue that this may be true for a variety of chemical and physical DNA damaging agents.
机译:真核DNA组织在核体中,该核肉组织,其包装DNA并调节其可行性与转录,复制,重组和修复。在这里,我们表明,在活细胞中,核肉保护DNA免受高能辐射和反应性氧。我们组合基于序列的方法(ATAC-SEQ和Bliss),以确定核心富含核心的恶性间皮瘤细胞基因组中的核体和双链断裂(DSB)的位置,以及部分核心耗尽的相同细胞。结果在人MCF-7乳腺癌细胞系中复制。我们发现,对于每个基因组序列,DSB形成的概率与核细胞组的一部分成比例成比例; DSBs从核心二元轴累积远端。活性转录基因的核小核心区域和启动子对DSB形成更敏感,从而突变。我们认为这可能是各种化学和物理DNA损伤剂可能的真实。

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