Efficient generation of recombinant adenoviral vectors by Cre-lox recombination in vitro
- PMID: 10448644
- PMCID: PMC2230325
Efficient generation of recombinant adenoviral vectors by Cre-lox recombination in vitro
Abstract
Background: Although recombinant adenovirus vectors are attractive for use in gene expression studies and therapeutic applications, the construction of these vectors remains relatively time-consuming. We report here a strategy that simplifies the production of adenoviruses using the Cre-loxP system.
Materials and methods: Full-length recombinant adenovirus DNA was generated in vitro by Cre-mediated recombination between loxP sites in a linearized shuttle plasmid containing a transgene and adenovirus genomic DNA.
Results: After transfection of Cre-treated DNA into 293 cells, replication-defective viral vectors were rapidly obtained without detectable wild-type virus.
Conclusion: This system facilitates the development of recombinant adenoviral vectors for basic and clinical research.
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