Resumen
DNA double-strand breaks (DSBs) are critical lesions that can lead to cell death or chromosomal rearrangements. Rad51 is necessary for most mitotic and meiotic DSB repair events, although a number of RAD51-independent pathways exist. Previously, we described DSB repair in rad51Δ yeast diploids that was stimulated by a DNA region termed "facilitator of break-induced replication" (FBI) located approximately 30 kb from the site of an HO-induced DSB. Here, we demonstrate that FBI is a large inverted DNA repeat that channels the repair of DSBs into the single-strand annealing-gross chromosomal rearrangements (SSA-GCR) pathway. Further, analysis of DSB repair in rad54Δ cells allowed us to propose that the SSA-GCR repair pathway is suppressed in the presence of Rad51p. Therefore, an additional role of Rad51 might be to protect eukaryotic genomes from instabilities by preventing chromosomal rearrangements.
| Idioma original | English (US) |
|---|---|
| Páginas (desde-hasta) | 9-18 |
| Número de páginas | 10 |
| Publicación | Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis |
| Volumen | 645 |
| N.º | 1-2 |
| DOI | |
| Estado | Published - oct 14 2008 |
| Publicado de forma externa | Sí |
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Health, Toxicology and Mutagenesis
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