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Differences in repair profiles of interstitial telomeric sites between normal and DNA double-strand break repair deficient Chinese hamster cells.
Rivero, María Teresa; Mosquera, Alejandro; Goyanes, Vicente; Slijepcevic, Predrag; Fernández, José Luis.
Afiliación
  • Rivero MT; Sección de Genétic y Unidad de Investigación, Hospital Teresa Herrera, Complejo Hospitalario, Universitario Juan Canalejo, As Xubias, La Coruña, Spain.
Exp Cell Res ; 295(1): 161-72, 2004 Apr 15.
Article en En | MEDLINE | ID: mdl-15051499
ABSTRACT
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.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Telómero / Reparación del ADN Límite: Animals Idioma: En Revista: Exp Cell Res Año: 2004 Tipo del documento: Article País de afiliación: España
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Telómero / Reparación del ADN Límite: Animals Idioma: En Revista: Exp Cell Res Año: 2004 Tipo del documento: Article País de afiliación: España