• Title of article

    Oligomeric Structure Diversity within the GIY-YIG Nuclease Family

  • Author/Authors

    Elena M. Ibryashkina، نويسنده , , Giedrius Sasnauskas، نويسنده , , Alexander S. Solonin، نويسنده , , Marina V. Zakharova، نويسنده , , Saulius Grazulis and Virginijus Siksnys، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2009
  • Pages
    7
  • From page
    10
  • To page
    16
  • 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.
  • Keywords
    Eco29kI , DNA–protein interaction , protein dimerization , GIY-YIG family , restriction endonuclease
  • Journal title
    Journal of Molecular Biology
  • Serial Year
    2009
  • Journal title
    Journal of Molecular Biology
  • Record number

    1258053