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Ionizing radiation-induced instant pairing of heterochromatin of homologous chromosomes in human cells

机译:电离辐射诱导人细胞中同源染色体异染色质的即时配对

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Using fluorescence in situ hybridization with human band-specific DNA probes we examined the effect of ionizing radiation on the intra-nuclear localization of the heterochromatic region 9q12→q13 and the euchromatic region 8p11.2 of similar sized chromosomes 9 and 8 respectively in confluent (G1) primary human fibroblasts. Microscopic analysis of the interphase nuclei revealed colocalization of the homologous heterochromatic regions from chromosome 9 in a proportion of cells directly after exposure to 4 Gy X-rays. The percentage of cells with paired chromosomes 9 gradually decreased to control levels during a period of one hour. No significant changes in localization were observed for chromosome 8. Using 2-D image analysis, radial and inter-homologue distances were measured for both chromosome bands. In unexposed cells, a random distribution of the chromosomes over the interphase nucleus was found. Directly after irradiation, the average inter-homologue distance decreased for chromosome 9 without alterations in radial distribution. The percentage of cells with inter-homologue distance <3 μm increased from 11% in control cells to 25% in irradiated cells. In contrast, irradiation did not result in significant changes in the inter-homologue distance for chromosome 8. Colocalization of the heterochromatic regions of homologous chromosomes 9 was not observed in cells irradiated on ice. This observation, together with the time dependency of the colocalization, suggests an underlying active cellular process. The biological relevance of the observed homologous pairing remains unclear. It might be related to a homology dependent repair process of ionizing radiation induced DNA damage that is specific for heterochromatin. However, also other more general cellular responses to radiation-induced stress or change in chromatin organization might be responsible for the observed pairing of heterochromatic regions.
机译:我们使用荧光原位杂交技术与人类条带特异性DNA探针进行了研究,研究了电离辐射对分别在相似大小的9号和8号染色体上的异色区9q12→q13和常色区8p11.2的核内定位的影响( G1)原代人成纤维细胞。对相间核的显微镜分析显示,暴露于4 Gy X射线后,在一定比例的细胞中,来自9号染色体的同源异色区域共定位。一小时内,具有成对染色体9的细胞百分比逐渐降低至控制水平。没有观察到染色体8的本地化显着变化。使用2-D图像分析,测量了两个染色体带的径向距离和同源间距离。在未暴露的细胞中,发现染色体在相间核上随机分布。辐照后,染色体9的平均同源间距离减小,而径向分布没有变化。同源间距离<3μm的细胞百分比从对照细胞的11%增加到受辐照细胞的25%。相反,辐照并没有导致染色体8的同源间距离发生显着变化。在冰上辐照的细胞中未观察到同源染色体9的异色区域的共定位。该观察结果以及共定位的时间依赖性表明存在潜在的活跃细胞过程。观察到的同源配对的生物学相关性仍不清楚。它可能与电离辐射引起的DNA损伤的异源性修复过程有关,该过程对异染色质具有特异性。但是,对辐射诱导的应激或染色质组织变化的其他更一般的细胞反应也可能是观察到的异色区域配对的原因。

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