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      Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae.

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          Abstract

          The budding yeast Saccharomyces cerevisiae has been the principal organism used in experiments to examine genetic recombination in eukaryotes. Studies over the past decade have shown that meiotic recombination and probably most mitotic recombination arise from the repair of double-strand breaks (DSBs). There are multiple pathways by which such DSBs can be repaired, including several homologous recombination pathways and still other nonhomologous mechanisms. Our understanding has also been greatly enriched by the characterization of many proteins involved in recombination and by insights that link aspects of DNA repair to chromosome replication. New molecular models of DSB-induced gene conversion are presented. This review encompasses these different aspects of DSB-induced recombination in Saccharomyces and attempts to relate genetic, molecular biological, and biochemical studies of the processes of DNA repair and recombination.

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          Author and article information

          Journal
          Microbiol Mol Biol Rev
          Microbiology and molecular biology reviews : MMBR
          American Society for Microbiology
          1092-2172
          1092-2172
          Jun 1999
          : 63
          : 2
          Affiliations
          [1 ] Rosenstiel Center and Department of Biology, Brandeis University, Waltham, Massachusetts 02454-9110, USA.
          Article
          10.1128/MMBR.63.2.349-404.1999
          98970
          10357855
          eead9ce6-ef0b-4d57-9d24-4805cf116015
          History

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