Junonia coenia densovirus-based vectors for stable transgene expression in Sf9 cells: influence of the densovirus sequences on genomic integration
| Autor: | Corinne Royer, Hervé Bossin, Sylvie Gimenez, Pierre Cérutti, Max Bergoin, Philippe Fournier, Patrick Barry, Pierre Couble |
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| Přispěvatelé: | Laviron, Nathalie |
| Jazyk: | angličtina |
| Rok vydání: | 2003 |
| Předmět: |
Concatemer
Virus Integration viruses Immunology Genetic Vectors Molecular Sequence Data Gene Dosage Genome Viral Biology Spodoptera Viral Nonstructural Proteins Transfection Microbiology Genome Green fluorescent protein chemistry.chemical_compound Plasmid Virology Animals Densovirus Transgenes Gene [SDV.BC] Life Sciences [q-bio]/Cellular Biology Genetics Base Sequence Gene Therapy Open reading frame chemistry Insect Science Plasmids |
| Popis: | The invertebrate parvovirus Junonia coenia densovirus (JcDNV) shares similarities with terminal hairpins and nonstructural (NS) protein activities of adeno-associated virus (AAV) despite their evolutionary divergence (B. Dumas, M. Jourdan, A. M. Pascaud, and M. Bergoin, Virology, 191:202-222, 1992, and C. Ding, M. Urabe, M. Bergoin, and R. M. Kotin, J. Virol. 76:338-345, 2002). We demonstrate here that persistent transgene expression in insect cells results from stable integration of transfected JcDNV-derived vectors into the host genome. To assess the integrative properties of JcDNV vectors, the green fluorescent protein (GFP) gfp marker gene was fused in frame into the major open reading frame (ORF1) of the viral sequence under the control of the P9 capsid protein promoter. In addition, the influence of the nonstructural proteins on the posttransfection maintenance of the vectors was examined by interruption of one or all three NS ORFs. Following transfection of Sf9 cells with each of the JcDNV constructs, clones showing persistent GFP expression were isolated. Structural analyses revealed that the majority of the JcDNV plasmid sequence was integrated into the genome of the fluorescent clones. Integration was observed whether or not NS proteins were expressed. However, the presence of NS genes in the constructs greatly influenced the number of integrated copies and their distribution in the host genome. Disruption of NS genes expression resulted in integration of head-to-tail concatemers at multiple sites within the genome. Further analyses demonstrated that the cis JcDNV 5′ inverted terminal repeat region was the primary site of recombination. Sequence analyses of integration junctions showed rearrangements of both flanking and internal sequences for most integrations. These findings demonstrate that JcDNV vectors integrate into insect cells in a manner similar to AAV plasmids in mammalian cells. |
| Databáze: | OpenAIRE |
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