RAD50 is required for efficient initiation of resection and recombinational repair at random, gamma-induced double-strand break ends

PLoS Genet. 2009 Sep;5(9):e1000656. doi: 10.1371/journal.pgen.1000656. Epub 2009 Sep 18.

Abstract

Resection of DNA double-strand break (DSB) ends is generally considered a critical determinant in pathways of DSB repair and genome stability. Unlike for enzymatically induced site-specific DSBs, little is known about processing of random "dirty-ended" DSBs created by DNA damaging agents such as ionizing radiation. Here we present a novel system for monitoring early events in the repair of random DSBs, based on our finding that single-strand tails generated by resection at the ends of large molecules in budding yeast decreases mobility during pulsed field gel electrophoresis (PFGE). We utilized this "PFGE-shift" to follow the fate of both ends of linear molecules generated by a single random DSB in circular chromosomes. Within 10 min after gamma-irradiation of G2/M arrested WT cells, there is a near-synchronous PFGE-shift of the linearized circular molecules, corresponding to resection of a few hundred bases. Resection at the radiation-induced DSBs continues so that by the time of significant repair of DSBs at 1 hr there is about 1-2 kb resection per DSB end. The PFGE-shift is comparable in WT and recombination-defective rad52 and rad51 strains but somewhat delayed in exo1 mutants. However, in rad50 and mre11 null mutants the initiation and generation of resected ends at radiation-induced DSB ends is greatly reduced in G2/M. Thus, the Rad50/Mre11/Xrs2 complex is responsible for rapid processing of most damaged ends into substrates that subsequently undergo recombinational repair. A similar requirement was found for RAD50 in asynchronously growing cells. Among the few molecules exhibiting shift in the rad50 mutant, the residual resection is consistent with resection at only one of the DSB ends. Surprisingly, within 1 hr after irradiation, double-length linear molecules are detected in the WT and rad50, but not in rad52, strains that are likely due to crossovers that are largely resection- and RAD50-independent.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Chromosomes, Fungal / metabolism
  • DNA Breaks, Double-Stranded / radiation effects*
  • DNA Repair / radiation effects*
  • DNA, Fungal / metabolism
  • DNA-Binding Proteins / metabolism*
  • Dimerization
  • Dose-Response Relationship, Radiation
  • Electrophoresis, Gel, Pulsed-Field
  • Exodeoxyribonucleases / metabolism
  • G2 Phase / radiation effects
  • Gamma Rays*
  • Mitosis / radiation effects
  • Mutation / genetics
  • Rad51 Recombinase / metabolism
  • Rad52 DNA Repair and Recombination Protein / metabolism
  • Recombination, Genetic / genetics*
  • Recombination, Genetic / radiation effects
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / radiation effects
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • DNA, Fungal
  • DNA-Binding Proteins
  • RAD50 protein, S cerevisiae
  • Rad52 DNA Repair and Recombination Protein
  • Saccharomyces cerevisiae Proteins
  • Rad51 Recombinase
  • Exodeoxyribonucleases
  • exodeoxyribonuclease I