Replicon rescue: a novel strategy to clone the genomic DNA flanking insertions of integrating shuttle vector DNA
Author(s) -
Tara L. McMahon,
Z. Wilczynska,
Christian Barth,
Derek Fraser,
Luisa Pontes,
Paul R. Fisher
Publication year - 1996
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/24.20.4096
Subject(s) - biology , replicon , plasmid , genetics , shuttle vector , cloning vector , molecular cloning , multiple cloning site , cloning (programming) , origin of replication , in vitro recombination , restriction map , microbiology and biotechnology , clone (java method) , gene , vector (molecular biology) , recombinant dna , peptide sequence , programming language , computer science
A novel cloning strategy, replicon rescue, was developed for cloning genes disrupted by plasmid insertions. After ligation to a tetracycline resistance cassette, fragments containing a bacterial origin of replication from the insertion are recovered in Escherichia coli because they replicate autonomously. Restriction enzymes for cloning are so chosen that the only legitimate two fragment ligation yielding TetR clones involves a fragment spanning the boundary of the insertion. Replicon rescue was used successfully firstly in a test system to clone the chromosomal orl from a Klebsiella aerogenes strain, and secondly to recover a disrupted gene from a phototaxis-deficient mutant of Dictyostelium.
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