| Literature DB >> 18755201 |
Brandon Downing1, Rachel Morgan, Kelly VanHulle, Angela Deem, Anna Malkova.
Abstract
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 rad51Delta yeast diploids that was stimulated by a DNA region termed "facilitator of break-induced replication" (FBI) located approximately 30kb 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 rad54Delta 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.Entities:
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Year: 2008 PMID: 18755201 PMCID: PMC2643024 DOI: 10.1016/j.mrfmmm.2008.07.013
Source DB: PubMed Journal: Mutat Res ISSN: 0027-5107 Impact factor: 2.433