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PMID: 16698548 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

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

Structure (London, England : 1993) ·Vol. 14 ·No. 5 ·2006-05-00 ·Pages 869-80

Spiegel PC, Chevalier B, Sussman D, Turmel M, Lemieux C, Stoddard BL

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.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Chlamydomonas/enzymology Crystallography, X-Ray DNA/chemistry Endodeoxyribonucleases/chemistry,classification Molecular Sequence Data Phylogeny Protein Conformation Protein Folding Substrate Specificity
Chemicals
DNA Endodeoxyribonucleases endodeoxyribonuclease I-CeuI
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Spiegel P Clint
Graduate Programs in Biomolecular Structure and Design and Molecular and Cellular Biology, University of Washington, Seattle, Washington 98195, USA.
Chevalier Brett
Sussman Django
Turmel Monique
Lemieux Claude
Stoddard Barry L
Article Info
Journal
Structure (London, England : 1993)
Abbr.
Structure
ISSN
0969-2126
Published
2006-05-00
Pages
869-80
Language
English
Region
United States
NLM ID
101087697
Subset
IM
Grants
NIGMS NIH HHS · GM49857 · United States
NCI NIH HHS · T32 CA80416 · United States
PHS HHS · T32 G08268 · United States
Corrections
CommentIn
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