Major advances in the use of site-specific recombinases to facilitate susta
ined gene expression via chromosomal targeting have been made during the pa
st year. New tools for genomic manipulations using this technology include
the discovery of epitopes in recombinases that confer nuclear localization,
crystal structures that show the precise topology of recombinase-DNA-subst
rate synaptic complexes, manipulations of the DNA recognition sequences tha
t select for integration over excision of DNA, and manipulations that make
changes in gene expression inducible by drug administration, in addition, e
ndogenous eukaryotic and mammalian DNA sequences have been discovered that
can support site-specific recombinase-mediated manipulations.