Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication

Science. 2011 Dec 23;334(6063):1713-6. doi: 10.1126/science.1210770.

Abstract

In eukaryotes, it is unknown whether mismatch repair (MMR) is temporally coupled to DNA replication and how strand-specific MMR is directed. We fused Saccharomyces cerevisiae MSH6 with cyclins to restrict the availability of the Msh2-Msh6 mismatch recognition complex to either S phase or G2/M phase of the cell cycle. The Msh6-S cyclin fusion was proficient for suppressing mutations at three loci that replicate at mid-S phase, whereas the Msh6-G2/M cyclin fusion was defective. However, the Msh6-G2/M cyclin fusion was functional for MMR at a very late-replicating region of the genome. In contrast, the heteroduplex rejection function of MMR during recombination was partially functional during both S phase and G2/M phase. These results indicate a temporal coupling of MMR, but not heteroduplex rejection, to DNA replication.

Publication types

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

MeSH terms

  • Cell Division
  • Cyclin B / genetics
  • Cyclin B / metabolism
  • DNA Mismatch Repair*
  • DNA Replication*
  • DNA, Fungal / metabolism*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Frameshift Mutation
  • G2 Phase
  • Genes, Fungal
  • Mutation
  • Nucleic Acid Heteroduplexes / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Recombination, Genetic
  • S Phase
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae / physiology
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • CLB2 protein, S cerevisiae
  • CLB6 protein, S cerevisiae
  • Cyclin B
  • DNA, Fungal
  • DNA-Binding Proteins
  • G-T mismatch-binding protein
  • Nucleic Acid Heteroduplexes
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins