Oligomeric structure diversity within the GIY-YIG nuclease family

J Mol Biol. 2009 Mar 20;387(1):10-6. doi: 10.1016/j.jmb.2009.01.048. Epub 2009 Jan 30.

Abstract

The GIY-YIG nuclease domain has been identified in homing endonucleases, DNA repair and recombination enzymes, and restriction endonucleases. The Type II restriction enzyme Eco29kI belongs to the GIY-YIG nuclease superfamily and, like most of other family members, including the homing endonuclease I-TevI, is a monomer. It recognizes the palindromic sequence 5'-CCGC/GG-3' ("/" marks the cleavage position) and cuts it to generate 3'-staggered ends. The Eco29kI monomer, which contains a single active site, either has to nick sequentially individual DNA strands or has to form dimers or even higher-order oligomers upon DNA binding to make a double-strand break at its target site. Here, we provide experimental evidence that Eco29kI monomers dimerize on a single cognate DNA molecule forming the catalytically active complex. The mechanism described here for Eco29kI differs from that of Cfr42I isoschisomer, which also belongs to the GIY-YIG family but is functional as a tetramer. This novel mechanism may have implications for the function of homing endonucleases and other enzymes of the GIY-YIG family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biopolymers / chemistry*
  • Biopolymers / metabolism
  • DNA / metabolism
  • Deoxyribonucleases, Type II Site-Specific / chemistry*
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Dimerization
  • Hydrolysis
  • Kinetics
  • Protein Conformation

Substances

  • Biopolymers
  • DNA
  • CCGCGG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific