Mutations altering the cleavage specificity of a homing endonuclease

Nucleic Acids Res. 2002 Sep 1;30(17):3870-9. doi: 10.1093/nar/gkf495.

Abstract

The homing endonuclease I-CreI recognizes and cleaves a particular 22 bp DNA sequence. The crystal structure of I-CreI bound to homing site DNA has previously been determined, leading to a number of predictions about specific protein-DNA contacts. We test these predictions by analyzing a set of endonuclease mutants and a complementary set of homing site mutants. We find evidence that all structurally predicted I-CreI/DNA contacts contribute to DNA recognition and show that these contacts differ greatly in terms of their relative importance. We also describe the isolation of a collection of altered specificity I-CreI derivatives. The in vitro DNA-binding and cleavage properties of two such endonucleases demonstrate that our genetic approach is effective in identifying homing endonucleases that recognize and cleave novel target sequences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Substitution
  • Base Sequence
  • Binding Sites / genetics
  • Binding, Competitive
  • DNA / genetics
  • DNA / metabolism*
  • DNA Restriction Enzymes / genetics
  • DNA Restriction Enzymes / metabolism*
  • Escherichia coli / genetics
  • Kinetics
  • Mutation
  • Plasmids / genetics
  • Sequence Homology, Nucleic Acid
  • Substrate Specificity

Substances

  • DNA
  • DNA Restriction Enzymes
  • endodeoxyribonuclease CreI