Relationship of DNA degradation by Saccharomyces cerevisiae Exonuclease 1 and its stimulation by RPA and Mre11-Rad50-Xrs2 to DNA end resection

Significance The repair of double-strand DNA breaks by homologous recombination is initiated by the nucleolytic resection of the 5′-terminated strand at the DNA break. Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2013-04, Vol.110 (18), p.E1661-E1668
Hauptverfasser: Cannavo, Elda, Cejka, Petr, Kowalczykowski, Stephen C
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Sprache:eng
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Zusammenfassung:Significance The repair of double-strand DNA breaks by homologous recombination is initiated by the nucleolytic resection of the 5′-terminated strand at the DNA break. Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo1. Here we investigated the relationship between the three nucleolytic complexes in vitro. With a focus on Exo1, we show that it is stimulated by the single-strand DNA-binding protein, RPA, and also by the Mre11-Rad50-Xrs2 complex. Furthermore, our analysis provides biochemical evidence for the view that Exo1 and Dna2-Sgs1-Top3-Rmi1 function downstream of Mre11-Rad50-Xrs2 as independent and mutually exclusive DNA end-processing pathways.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1305166110