© BioMed Central Ltd 2001
Published: 01 June 2001
Homologous recombination of DNA is a powerful tool for chromosome engineering experiments, but is a rare event, requiring long stretches of homology and complex reactions. Phage-mediated systems allow efficient recombination of linear DNA with relatively short homologies. In the June 5 Proceedings of the National Academy of Sciences, Ellis et al. describe an efficient recombination system that uses short synthetic single-stranded DNA (ssDNA) (Proc Natl Acad Sci USA 2001, 98:6742-6746). They show that oligonucleotides as short as 30 nucleotides could be used to correct 'amber' mutations in the E. coli galKgene using the bacteriophage lambda Red system (with efficiencies up to 6%). Only the lambda Beta protein is absolutely required for ssDNA recombination. The authors propose a recombination mechanism in which the Beta protein binds and anneals the ssDNA to a complimentary single-strand near the DNA replication fork. They suggest that ssDNA may prove useful for chromosome modification and repair in eukaryotic cells.
- An efficient recombination system for chromosome engineering in Escherichia coli.
- Proceedings of the National Academy of Sciences, [http://www.pnas.org]