1. Upstream AP1- and CREB-Binding Sites Confer High Basal Activity on the Adeno-Associated Virus Type 5 Capsid Gene Promoter
- Author
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David J. Pintel and Chaoyang Ye
- Subjects
viruses ,Molecular Sequence Data ,Immunology ,CREB ,medicine.disease_cause ,Microbiology ,Cell Line ,Capsid ,Genes, Reporter ,Sequence Homology, Nucleic Acid ,Virology ,medicine ,Humans ,Cyclic AMP Response Element-Binding Protein ,Luciferases ,Promoter Regions, Genetic ,Adeno-associated virus ,Transcription factor ,Gene ,Binding Sites ,Base Sequence ,biology ,HEK 293 cells ,Promoter ,Dependovirus ,Molecular biology ,Genome Replication and Regulation of Viral Gene Expression ,Transcription Factor AP-1 ,AP-1 transcription factor ,Insect Science ,biology.protein ,HeLa Cells ,Plasmids - Abstract
In contrast to the prototype adeno-associated virus type 2 (AAV2), the capsid gene P41 promoter of AAV5, within viral constructs that lack inverted terminal repeat sequences, displays a high basal level of expression in 293 cells in the absence of coinfecting adenovirus. Here we demonstrate that this was due to differences in the relative strengths of the core promoter elements and to the presence of active binding sites for the transcription factors CREB and AP1 within the upstream region of P41 that are absent from the AAV2 capsid gene promoter P40. These differences also governed the relative basal activity of the AAV capsid gene promoters within near-full-length viral genomes.
- Published
- 2007
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