Title: I-PpoI and I-CreI homing site sequence degeneracy determined by random mutagenesis and sequential in vitro enrichment.
Authors: Argast, G M; Stephens, K M; Emond, M J; Monnat Jr, R J
Published In J Mol Biol, (1998 Jul 17)
Abstract: Plasmid libraries containing partially randomized cleavage sites for the eukaryotic homing endonucleases I-PpoI and I-CreI were constructed, and sites that could be cleaved by I-PpoI or I-CreI were selectively recovered by successive cycles of cleavage and gel separation followed by religation and growth in Escherichia coli. Twenty-one different I-PpoI-sensitive homing sites, including the native homing site, were isolated. These sites were identical at four nucleotide positions within the 15 bp homing site, had a restricted pattern of base substitutions at the remaining 11 positions and displayed a preference for purines flanking the top strand of the homing site sequence. Twenty-one different I-CreI-sensitive homing sites, including the native site, were isolated. Ten nucleotide positions were identical in homing site variants that were I-CreI-sensitive and required the addition of SDS for efficient cleavage product release. Four of these ten positions were identical in homing sites that did not require SDS for product release. There was a preference for pyrimidines flanking the top strand of the homing site sequence. Three of the 24 I-CreI homing site nucleotide positions apparently lacked informational content, i. e. were permissive of cleavage when occupied by any nucleotide. These results suggest that I-PpoI and I-CreI make a large number of DNA-protein contacts across their homing site sequences, and that different subsets of these contacts may be sufficient to maintain a high degree of sequence-specific homing site recognition and cleavage. The sequential enrichment protocol we used should be useful for defining the sequence degeneracy and informational content of other homing endonuclease target sites.
PubMed ID: 9665841
MeSH Terms: Base Sequence; Binding Sites; DNA Restriction Enzymes/genetics; DNA Restriction Enzymes/metabolism*; Endodeoxyribonucleases/genetics; Endodeoxyribonucleases/metabolism*; Escherichia coli/genetics; Introns/genetics; Molecular Sequence Data; Mutagenesis*; Plasmids/genetics; Research Support, U.S. Gov't, P.H.S.; Sequence Alignment; Substrate Specificity