Differences in repair profiles of interstitial telomeric sites between normal and DNA double-strand break repair deficient Chinese hamster cells

被引:27
作者
Rivero, MT
Mosquera, A
Goyanes, V
Slijepcevic, P
Fernández, JL
机构
[1] Ctr Oncol Galicia, Lab Genet Mol & Radiobiol, La Coruna 15009, Spain
[2] Brunel Univ, Dept Biol Sci, Uxbridge UB8 3PH, Middx, England
[3] Complejo Hosp Univ Juan Canalejo, Secc Genet, Hosp Teresa Herrera, La Coruna 15006, Spain
[4] Complejo Hosp Univ Juan Canalejo, Unidad Invest, Hosp Teresa Herrera, La Coruna 15006, Spain
关键词
DBD-FISH; comet assay; interstitial telomeric sequences; DNA single-strand breaks; DNA double-strand breaks; ionizing radiation; homologous recombination; non-homologous end joining;
D O I
10.1016/j.yexcr.2003.12.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Interstitial Telomeric Repeat Sequence (ITRS) blocks are recognized as hot spots for spontaneous and ionizing radiation-induced chromosome breakage and recombination. Background and ionizing radiation-induced DNA breaks in large blocks of ITRS from Chinese hamster cell lines were analyzed using the DNA Breakage Detection-Fluorescence In Situ Hybridization (DBD-FISH) procedure. Our results indicate an extremely alkali-sensitivity of ITRS. Furthermore, it appears that ITRS blocks exhibit a particular chromatin structure, being enriched in short unpaired DNA segments. These segments could be liable to severe topological stress in highly compacted areas of the genome resulting in their spontaneous fragility and thus explaining their alkali-sensitivity. The induction and repair kinetics of DNA single-strand breaks (ssb) and DNA double-strand breaks (dsb) induced by ionizing radiation were assessed by DBD-FISH on neutral comets using Chinese hamster cells deficient in either DNA-PKcs or Rad51C. Our results indicate that the initial rejoining rate of dsb within ITRS is slower than that in the whole genome, in wild-type cells, demonstrating an intragenomic heterogeneity in dsb repair. Interestingly, in the absence of DNA-PKcs activity, the rejoining rate of dsb within ITRS is not modified, unlike in the whole genome. This was also found in the case of Rad51C mutant cells. Our results suggest the possibility that different DNA sequences or chromatin organizations may be targeted by specific dsb repair pathways. Furthermore, it appears that additional unknown dsb repair pathways may be operational in mammalian cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:161 / 172
页数:12
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