A novel adenovirus vector for easy cloning in the E3 region downstream of the CMV promoter
© Mailly et al; licensee BioMed Central Ltd. 2008
Received: 04 April 2008
Accepted: 06 June 2008
Published: 06 June 2008
The construction of expression vectors derived from the human adenovirus type 5 (Ad5), usually based on homologous recombination, is time consuming as a shuttle plasmid has to be selected before recombination with the viral genome. Here, we describe a method allowing direct cloning of a transgene in the E3 region of the Ad5 genome already containing the immediate early CMV promoter upstream of three unique restriction sites. This allowed the construction of recombinant adenoviral genomes in just one step, reducing considerably the time of selection and, of course, production of the corresponding vectors. Using this vector, we produced recombinant adenoviruses, each giving high-level expression of the transgene in the transduced cells.
The most commonly used method for generating recombinant adenoviral vectors is based on homologous recombination in E. coli [1, 2]. This method requires a first cloning step into a shuttle plasmid containing a promoter for the expression of the transgene. After selection of recombinants, the plasmid DNA of each clone has to be transferred into an other bacterial strain (i.e. DH5α, DH10b) because the homologous recombination is performed with BJ5183 E. coli strain  that does not allow for production of large quantities of plasmid. Improvements to this method have been made by using Top10F' bacteria that produce a high copy number of plasmids  or in vitro ligation for the subcloning of a gene of interest in the viral genome [5–7]. However, although these techniques allow efficient generation of recombinant adenoviral genomes, two-step plasmid manipulation is necessary.
Oligonucleotides used in this study (restriction sites are in bold)
Oligonucleotides used for:
length of amplified fragments (bp)
Amplification of E3 flanking regions
Insertion of TCS in adenovirus genome
GATAACAGATTTAAAT CCTTCGAA CAGAATCGAT
GGCCATCGAT TCTGTTCGAA GGATTTAAAT CTGTT
PCR to check pAd5CMV/TCS
EGFP amplification from pEGFPC3
PCR to check pAd5CMV-EGFP
Amplification of TK from pMBP-TK
Four different constructs were inserted into pAd5CMV/TCS to drive the expression of either the enhanced green fluorescent protein (EGFP), thymidine kinase from Herpes Simplex Virus type 1 (TK), a TK/EGFP fusion protein or a mutated form of the HPV16 E6 protein (Fig. 1A) . The EGFP ORF and the SV40 polyadenylation site from the pEGFP-C3 (Clontech, Saint-Germain en Laye, France) was inserted using the Swa I and Cla I restriction sites after PCR amplification (primers are listed in Table 1). For the resulting plasmid, pAd5-EGFP, it is possible to exchange the EGFP ORF (using Swa I and Bst BI) while keeping the SV40 polyadenylation site (Fig 1A).
The TK ORF was PCR-amplified from pMBP-TK  and inserted into pAd5-EGFP either in replacement of the EGFP ORF (Swa I-Bst BI) or fused upstream of the EGFP coding sequence (Swa I). E6mut, a flag-tagged dominant negative mutant of HPV16 E6 protein (E6-6C/6S-F47R-ΔPDZ), was also successfully sub-cloned . This was achieved by inserting a Klenow-repaired Eco RI fragment containing the E6mut ORF into the Swa I site of pAd5CMV/TCS. For each construction, a good ratio of positive clones was obtained, respectively 14/20, 6/20, 12/20 and 3/10, in only three days (from the start of cloning until the plasmid preparation and restriction verification).
The four corresponding recombinant adenoviruses were produced in 293 cells following classical procedures  and tested on HeLa cells. The expression of the different proteins was examined by Western blotting (Fig 1B), EGFP fluorescence and immunofluorescence (Fig 1C). This demonstrated that (i) cells are were efficiently transduced, (ii) the fusion protein TK/EGFP conserved the green fluorescence conferred by its EGFP moiety, (iii) the fusion TK/EGFP conserved the TK epitopes, and (iv) the E6 mutant protein was well expressed and recognized by both anti-E6 and anti-Flag antibodies. Cells expressing TK are sensitive to the pro-drug ganciclovir and the ability of the fusion product to induce cell death was investigated using a Methylthiazolyldiphenyl-tetrazolium bromide (MTT) assay (Fig. 1D). This test demonstrated that both TK and TK/EGFP induced the death of HeLa cells after treatment with ganciclovir.
This approach can be easily used in any laboratory to rapidly produce recombinant adenoviruses. For this, a new vector derived from Ad5 has been created by inserting, in replacement of the E3 region, the CMVp followed by three unique restriction sites (Swa I, Bst BI,Cla I) that are absent from a ΔE1 Ad5 genome. This triple cloning site allows the easy cloning of a transgene that will be expressed from the CMVp. In addition, pAd5-EGFP, allows the cloning a cDNA of interest between the CMV promoter and the SV40 polyadenylation signal either in replacement of the EGFP ORF or in fusion with it. This is also possible with this vector to clone a second transgene in the E1 region by using homologous recombination in E. coli as previously described . Four different transgenes were inserted into pAd5CMV/TCS. The construction of the corresponding genomes, contained in plasmids, was rapidly achieved (3 days instead of 7 to 10 days with homologous recombination in E. coli). In each case, a much higher proportion of positive clones after ligation into pAdCMV5-TCS (30–70%) was obtained when compared to homologous recombination (15% at best in our laboratory). The constructs led to the production of infectious adenoviral particles that allowed the high-level expression of the different transgenes. This method of construction of adenovirus vectors is clearly faster and easier than conventional approaches and can be used by those who are not familiar with the homologous recombination system.
We acknowledge Emiliana Borrelli (IGBMC, Strasbourg) and the Transgene company (Strasbourg) for the gift of plasmids and Philip Robinson (CHU Bordeaux) for careful reading and fruitful discussion. This work was supported by the Université Louis Pasteur de Strasbourg, the Centre National de la Recherche Scientifique, the Association pour la Recherche contre le Cancer, the Ligue Nationale Contre Le Cancer and the Cancéropôle-Grand-EST. L.M. was supported by a postdoctoral fellowship from the Cancéropôle-Grand-EST and C.B-L was supported by the Ministère de la Recherche.
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