Engineering spacer specificity of the Cre/loxP system

Nucleic Acids Res. 2024 Jul 22;52(13):8017-8031. doi: 10.1093/nar/gkae481.

Abstract

Translational research on the Cre/loxP recombination system focuses on enhancing its specificity by modifying Cre/DNA interactions. Despite extensive efforts, the exact mechanisms governing Cre discrimination between substrates remains elusive. Cre recognizes 13 bp inverted repeats, initiating recombination in the 8 bp spacer region. While literature suggests that efficient recombination proceeds between lox sites with non-loxP spacer sequences when both lox sites have matching spacers, experimental validation for this assumption is lacking. To fill this gap, we investigated target site variations of identical pairs of the loxP 8 bp spacer region, screening 6000 unique loxP-like sequences. Approximately 84% of these sites exhibited efficient recombination, affirming the plasticity of spacer sequences for catalysis. However, certain spacers negatively impacted recombination, emphasizing sequence dependence. Directed evolution of Cre on inefficiently recombined spacers not only yielded recombinases with enhanced activity but also mutants with reprogrammed selective activity. Mutations altering spacer specificity were identified, and molecular modelling and dynamics simulations were used to investigate the possible mechanisms behind the specificity switch. Our findings highlight the potential to fine-tune site-specific recombinases for spacer sequence specificity, offering a novel concept to enhance the applied properties of designer-recombinases for genome engineering applications.

MeSH terms

  • DNA / chemistry
  • DNA / genetics
  • DNA, Intergenic / chemistry
  • DNA, Intergenic / genetics
  • Directed Molecular Evolution / methods
  • Integrases* / chemistry
  • Integrases* / genetics
  • Integrases* / metabolism
  • Mutation
  • Recombination, Genetic*
  • Substrate Specificity

Substances

  • Integrases
  • Cre recombinase
  • DNA
  • DNA, Intergenic