We have recently developed a high-efficiency method of constructing adenovi
rus vectors based on Cre-mediated recombination between two plasmids co-tra
nsfected into 293 cells. The simplicity and efficiency of this method shoul
d greatly expedite the construction of most recombinant vectors. However th
is system would not be suitable for constructing vectors bearing loxP sites
elsewhere in the genome because of undesirable Cre-mediated vector rearran
gements. To address this, we have developed a similar system using FLP-medi
ated sites-specific recombination for the construction of adenovirus vector
s.