The structure of I-CeuI homing endonuclease: Evolving asymmetric DNA recognition from a symmetric protein scaffold

Structure. 2006 May;14(5):869-80. doi: 10.1016/j.str.2006.03.009.

Abstract

Homing endonucleases are highly specific catalysts of DNA strand breaks, leading to the transfer of mobile intervening sequences containing the endonuclease ORF. We have determined the structure and DNA recognition behavior of I-CeuI, a homodimeric LAGLIDADG endonuclease from Chlamydomonas eugametos. This symmetric endonuclease displays unique structural elaborations on its core enzyme fold, and it preferentially cleaves a highly asymmetric target site. This latter property represents an early step, prior to gene fusion, in the generation of asymmetric DNA binding platforms from homodimeric ancestors. The divergence of the sequence, structure, and target recognition behavior of homing endonucleases, as illustrated by this study, leads to the invasion of novel genomic sites by mobile introns during evolution.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Chlamydomonas / enzymology*
  • Crystallography, X-Ray
  • DNA / chemistry*
  • Endodeoxyribonucleases / chemistry*
  • Endodeoxyribonucleases / classification
  • Molecular Sequence Data
  • Phylogeny
  • Protein Conformation
  • Protein Folding
  • Substrate Specificity

Substances

  • DNA
  • Endodeoxyribonucleases
  • endodeoxyribonuclease I-CeuI