Highly efficient phage-based Escherichia coli homologous recombination syst
ems have recently been developed that enable genomic DNA in bacterial artif
icial chromosomes to be modified and subcloned, without the need for restri
ction enzymes or DNA ligases. This new form of chromosome engineering, term
ed recombinogenic engineering or recombineering, is efficient and greatly d
ecreases the time it takes to create transgenic mouse models by traditional
means, Recombineering also facilitates many kinds of genomic experiment th
at have otherwise been difficult to carry out, and should enhance functiona
l genomic studies by providing better mouse models and a more refined genet
ic analysis of the mouse genome.