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FEMS Microbiol Lett. 1998 Jan 1;158(1):75-81.

A reliable amplification technique for the characterization of genomic DNA sequences flanking insertion sequences.

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1
Centre national de référence des mycobactéries, Institut Pasteur, Paris, France.

Abstract

A simple and efficient ligation-mediated PCR (LMPCR) is described for amplifying DNA adjacent to known sequences. The method uses one primer specific for the known sequence and a second specific for a synthetic linker ligated to restricted genomic DNA. Perkin-Elmer AmpliTaq Gold polymerase is used to minimize non-specific primer annealing and amplification. This LMPCR method was successfully applied to isolate DNA sequences flanking mobile elements present in mycobacterial mutants generated by transposon mutagenesis.

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