New adenovirus vectors for protein production and gene transfer

• Published in: Cytotechnology (Dordrecht) 1998-11, Vol.28 (1-3), p.53-64
• Main Authors: Massie, B, Mosser, D D, Koutroumanis, M, Vitté-Mony, I, Lamoureux, L, Couture, F, Paquet, L, Guilbault, C, Dionne, J, Chahla, D, Jolicoeur, P, Langelier, Y
• Format: Article
• Language: English
• Subjects: Adenoviruses; Cell lines; Cytomegalovirus; Cytotoxicity; Expression vectors; Gene transfer; Genes; Green fluorescent protein; Protein folding; Proteins; Recombinants; Replication
• ISSN: 0920-9069; 1573-0778
• DOI: 10.1023/a:1008013211222

Based on two new adenovirus expression cassettes, we have constructed a series of Ad transfer vectors for the overexpression of one or two genes either in a dicistronic configuration or with separate expression cassettes. Inclusion of the green or blue fluorescent protein in the vectors accelerates the generation of adenovirus recombinants and facilitates the functional characterization of genes both in vitro and in vivo by allowing easy quantification of gene transfer and expression. With our optimized tetracycline-regulated promoter (TR5) we have generated recombinant adenoviruses expressing proteins, that are either cytotoxic or which interfere with adenovirus replication, at levels of 10-15% of total cell protein. Proteins that are not cytotoxic can be produced at levels greater than 20% of total cell protein. As well, these levels of protein production can be achieved with or without adenovirus replication. This yield is similar to what can be obtained with our optimized human cytomegalovirus-immediate early promoter-enhancer (CMV5) for constitutive protein expression in non-complementing cell lines. Using the green fluorescent protein as a reporter, we have shown that a pAdCMV5-derived adenovirus vector expresses about 6-fold more protein in complementing 293 cells and about 12-fold more in non- complementing HeLa cells than an adenovirus vector containing the standard cytomegalovirus promoter. Moreover, a red-shifted variant of green fluorescent protein incorporated in one series of vectors was 12-fold more fluorescent than the S65T mutant, making the detection of the reporter protein possible at much lower levels of expression.