首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Effect of Wortmannin on the repair profiles of DNA double-strand breaks in the whole genome and in interstitial telomeric sequences of Chinese hamster cells.
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Effect of Wortmannin on the repair profiles of DNA double-strand breaks in the whole genome and in interstitial telomeric sequences of Chinese hamster cells.

机译:渥曼青霉素对中国仓鼠细胞全基因组和间质端粒序列DNA双链断裂修复模式的影响。

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The DNA breakage detection-fluorescence in situ hybridization (DBD-FISH) procedure was applied to analyze the effect of Wortmannin (WM) in the rejoining kinetics of ionizing radiation-induced DNA double-strand breaks (DSBs) in the whole genome and in the long interstitial telomeric repeat sequence (ITRS) blocks from Chinese hamster cell lines. The results indicate that the ITRS blocks from wild-type Chinese hamster cell lines, CHO9 and V79B, exhibit a slower initial rejoining rate of ionizing radiation-induced DSBs than the genome overall. Neither Rad51C nor the catalytic subunit of DNA-dependent protein kinase (DNA-PKcs) activities, involved in homologous recombination (HR) and in non-homologous end-joining (NHEJ) pathways of DSB repair respectively, influenced the rejoining kinetics within ITRS in contrast to DNA sequences in the whole genome. Nevertheless, DSB removal rate within ITRS was decreased in the absence of Ku86 activity, though at a lower affectation level than in the whole genome, thus homogenizing both rejoining kinetics rates. WM treatment slowed down the DSB rejoining kinetics rate in ITRS, this effect being more pronounced in the whole genome, resulting in a similar pattern to that of the Ku86 deficient cells. In fact, no WM effect was detected in the Ku86 deficient Chinese hamster cells, so probably WM does not add further impairment in DSB rejoining than that resulted as a consequence of absence of Ku activity. The same slowing effect was also observed after treatment of Rad51C and DNA-PKcs defective hamster cells by WM, suggesting that: (1) there is no potentiation of the HR when the NHEJ is impaired by WM, either in the whole genome or in the ITRS, and (2) that this impairment may probably involve more targets than DNA-PKcs. These results suggest that there is an intragenomic heterogeneity in DSB repair, as well as in the effect of WM on this process.
机译:DNA断裂检测-荧光原位杂交(DBD-FISH)方法用于分析Wortmannin(WM)在整个基因组和整个细胞中电离辐射诱导的DNA双链断裂(DSBs)的重新结合动力学中的作用。中国仓鼠细胞系的长间隙端粒重复序列(ITRS)块。结果表明,野生型中国仓鼠细胞系CHO9和V79B的ITRS阻滞比电离辐射诱导的DSB的初始重新结合速率慢于整个基因组。无论是Rad51C还是DNA依赖性蛋白激酶(DNA-PKcs)活性的催化亚基,分别参与DSB修复的同源重组(HR)和非同源末端连接(NHEJ)途径,都不会影响ITRS内的重新结合动力学。与整个基因组中的DNA序列形成对比。尽管如此,在不存在Ku86活性的情况下,ITRS中的DSB去除率却降低了,尽管其影响水平低于整个基因组中的水平,从而使两个重新结合的动力学率均一。 WM处理减慢了ITRS中DSB的重新结合动力学速率,这种作用在整个基因组中更加明显,从而导致与Ku86缺陷细胞相似的模式。实际上,在缺乏Ku86的中国仓鼠细胞中未检测到WM效应,因此,与由于缺乏Ku活性而导致的DSB重新结合相比,WM可能不会进一步增加DSB再结合的损伤。 WM处理Rad51C和DNA-PKcs缺陷的仓鼠细胞后,也观察到了相同的减慢作用,这表明:(1)当WM损害NHEJ时,无论是在整个基因组中还是在HME中,HR均无增强作用。 ITRS,(2)与DNA-PKcs相比,这种损伤可能涉及更多的靶标。这些结果表明,DSB修复中存在基因组内异质性,以及WM在此过程中的影响。

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