The Nse5-Nse6 dimer mediates DNA repair roles of the Smc5-Smc6 complex

Mol Cell Biol. 2006 Mar;26(5):1617-30. doi: 10.1128/MCB.26.5.1617-1630.2006.

Abstract

Stabilization and processing of stalled replication forks is critical for cell survival and genomic integrity. We characterize a novel DNA repair heterodimer of Nse5 and Nse6, which are nonessential nuclear proteins critical for chromosome segregation in fission yeast. The Nse5/6 dimer facilitates DNA repair as part of the Smc5-Smc6 holocomplex (Smc5/6), the basic architecture of which we define. Nse5-Nse6 [corrected] (Nse5 and Nse6) [corrected] mutants display a high level of spontaneous DNA damage and mitotic catastrophe in the absence of the master checkpoint regulator Rad3 (hATR). Nse5/6 mutants are required for the response to genotoxic agents that block the progression of replication forks, acting in a pathway that allows the tolerance of irreparable UV lesions. Interestingly, the UV sensitivity of Nse5/6 [corrected] is suppressed by concomitant deletion of the homologous recombination repair factor, Rhp51 (Rad51). Further, the viability of Nse5/6 mutants depends on Mus81 and Rqh1, factors that resolve or prevent the formation of Holliday junctions. Consistently, the UV sensitivity of cells lacking Nse5/6 can be partially suppressed by overexpressing the bacterial resolvase RusA. We propose a role for Nse5/6 mutants in suppressing recombination that results in Holliday junction formation or in Holliday junction resolution.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism*
  • DNA Helicases / genetics
  • DNA Helicases / metabolism
  • DNA Repair / physiology*
  • DNA Replication / physiology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Dimerization
  • Endonucleases / genetics
  • Endonucleases / metabolism
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Genome, Fungal / genetics
  • Genomic Instability
  • Holliday Junction Resolvases / genetics
  • Holliday Junction Resolvases / metabolism
  • Multiprotein Complexes
  • Mutation
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Recombination, Genetic
  • Schizosaccharomyces / genetics
  • Schizosaccharomyces / radiation effects
  • Schizosaccharomyces pombe Proteins / genetics
  • Schizosaccharomyces pombe Proteins / metabolism*
  • Ultraviolet Rays

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • MUS81 protein, S pombe
  • Multiprotein Complexes
  • Nse5 protein, S pombe
  • Nse6 protein, S pombe
  • Nuclear Proteins
  • Recombinant Proteins
  • Schizosaccharomyces pombe Proteins
  • Smc5 protein, S pombe
  • smc6 protein, S pombe
  • Endonucleases
  • Holliday Junction Resolvases
  • RusA protein, E coli
  • DNA Helicases
  • Rqh1 protein, S pombe