Preparation and Resolution of Holliday Junction DNA Recombination Intermediates

Methods Enzymol. 2018:600:569-590. doi: 10.1016/bs.mie.2017.11.022. Epub 2018 Jan 9.

Abstract

Holliday junctions provide a covalent link between recombining DNA molecules and need to be removed prior to chromosome segregation at mitosis. Defects in their resolution lead to mitotic catastrophe, characterized by the formation of DNA breaks and chromosome aberrations. Enzymes that resolve recombination intermediates have been identified in all forms of life, from bacteriophage, to bacteria, yeast, and humans. In higher eukaryotes, Holliday junctions are resolved by GEN1, a nuclease that is mechanistically similar to the prototypic resolvase Escherichia coli RuvC, and by the SMX trinuclease complex. Studies of these enzymes have been facilitated by the use of plasmid-sized DNA recombination intermediates made by RecA-mediated strand exchange. Here, we detail the preparation of these recombination intermediates, which resemble α-structures, and their resolution by RuvC and GEN1.

Keywords: Branch migration; DNA repair; GEN1; Resolvase; RuvC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA, Cruciform / chemistry*
  • DNA, Single-Stranded / chemistry*
  • DNA, Single-Stranded / isolation & purification
  • Endodeoxyribonucleases / chemistry*
  • Endodeoxyribonucleases / isolation & purification
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / isolation & purification
  • Holliday Junction Resolvases / chemistry*
  • Holliday Junction Resolvases / isolation & purification
  • Isotope Labeling / instrumentation
  • Isotope Labeling / methods
  • Phosphorus Radioisotopes / chemistry
  • Recombinational DNA Repair*

Substances

  • DNA, Cruciform
  • DNA, Single-Stranded
  • Escherichia coli Proteins
  • Phosphorus Radioisotopes
  • ruvC protein, E coli
  • Phosphorus-32
  • Endodeoxyribonucleases
  • GEN1 protein, human
  • Holliday Junction Resolvases