Real-time tracking reveals catalytic roles for the two DNA binding sites of Rad51

Nat Commun. 2020 Jun 11;11(1):2950. doi: 10.1038/s41467-020-16750-3.

Abstract

During homologous recombination, Rad51 forms a nucleoprotein filament on single-stranded DNA to promote DNA strand exchange. This filament binds to double-stranded DNA (dsDNA), searches for homology, and promotes transfer of the complementary strand, producing a new heteroduplex. Strand exchange proceeds via two distinct three-strand intermediates, C1 and C2. C1 contains the intact donor dsDNA whereas C2 contains newly formed heteroduplex DNA. Here, we show that the conserved DNA binding motifs, loop 1 (L1) and loop 2 (L2) in site I of Rad51, play distinct roles in this process. L1 is involved in formation of the C1 complex whereas L2 mediates the C1-C2 transition, producing the heteroduplex. Another DNA binding motif, site II, serves as the DNA entry position for initial Rad51 filament formation, as well as for donor dsDNA incorporation. Our study provides a comprehensive molecular model for the catalytic process of strand exchange mediated by eukaryotic RecA-family recombinases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Binding Sites / genetics
  • DNA / genetics
  • DNA / metabolism*
  • DNA Damage / genetics
  • DNA Damage / physiology
  • DNA Repair / genetics
  • DNA Repair / physiology
  • DNA, Single-Stranded / genetics
  • Homologous Recombination / genetics
  • Homologous Recombination / physiology
  • Humans
  • Mutation / genetics
  • Nucleic Acid Heteroduplexes / genetics
  • Nucleic Acid Heteroduplexes / metabolism
  • Protein Structure, Secondary
  • Rad51 Recombinase / chemistry*
  • Rad51 Recombinase / genetics
  • Rad51 Recombinase / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Schizosaccharomyces / genetics

Substances

  • DNA, Single-Stranded
  • Nucleic Acid Heteroduplexes
  • Adenosine Triphosphate
  • DNA
  • Rad51 Recombinase