Adenoviruses for control of gene expression
AssigneeAdVec, Inc.
InventorsFrank L. Graham, Martina Anton, Silvia Bacchetti, Ping Wang, Michael A. Rudnicki, William J. Muller
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Abstract
The invention claims a class of adenovirus vectors for delivering recombinases to a large number of cells of different origins, and methods for regulating the expression of a gene in transfected mammalian cells in culture and in cells of transgenic animals, comprising infecting said cells with an Ad vector encoding a recombinase whose target site is present at or adjacent to the gene, wherein the action of the recombinase regulates the expression of said gene.
Claims15
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, and site-specific recombinase target sites positioned to remove or invert a portion of the expression cassette, whereby recombination between said target sites mediated by a site-specific recombinase alters expression of the coding sequence of the gene.
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, and site-specific recombinase target sites flanking the promoter sequence of said expression cassette that promotes expression of the gene, whereby recombination between said target sites mediated by a site-specific recombinase removes the promoter sequence, resulting in decreased expression of the coding sequence of the gene.
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, the promoter sequence directed away from said gene, and two site-specific recombinase target sites flanking said promoter sequence but oriented in opposite orientation to one another, whereby recombination between said target sites mediated by a site-specific recombinase inverts the promoter sequence, resulting in increased expression of the coding sequence of the gene.
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, a DNA spacer sequence located between the promoter sequence and the coding sequence, and a transcription termination site, and site-specific recombinase target sites flanking the DNA spacer sequence, whereby recombination between said target sites mediated by a site-specific recombinase removes the DNA spacer sequence, resulting in increased expression of the coding sequence of the gene.
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, and site-specific recombinase target sites flanking the coding sequence of the gene, whereby recombination between said target sites mediated by a site-specific recombinase removes the coding sequence, resulting in decreased of the coding sequence of the gene.
An adenovirus comprising an inserted expression cassette comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, a portion of said expression cassette comprising the coding sequence oriented in an opposite direction to normal translation of the coding sequence of the gene, and two site-specific recombinase target sites flanking said coding sequence but oriented in opposite orientation to one another, whereby recombination between said target sites mediated by a site-specific recombinase inverts the coding sequence, resulting in increased expression of the coding sequence of the gene.
An adenovirus comprising a promoter sequence, a coding sequence of a gene, a transcription termination site, and site-specific recombinase target sites flanking the coding sequence of the gene, whereby recombination between said target sites mediated by a site-specific recombinase removes the coding sequence of the gene, resulting in decreased expression of the gene.
An adenovirus comprising a promoter sequence, a coding sequence of a gene, and a transcription termination site, said coding sequence of the gene oriented in an opposite direction to normal translation of the gene, and two site-specific recombinase target sites flanking said coding sequence of the gene but oriented in opposite orientation to one another, whereby recombination between said target sites mediated by a site-specific recombinase inverts the gene, resulting in increased expression of the coding sequence of the gene.
Dependencies are inferred from the claim text.