AAV and Adenoviral Vectors (4)

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Schematic of Plasmid Amplification in Recombinase Deficient e. Coli
 Schematic of targeted gene knock-out (left) and targeted DNA knock-in (right) by CRISPR/Cas9. Adenoviral CRISPR vectors (left) or CRISPR vectors and donor DNA vectors (right) are transduced to target cells. Within target cells, Cas9 machinery is transiently expressed and binds to target DNA. In the final step of targeted gene knock-out (left), a fragment is deleted from two homologous strands of DNA through error-prone non-homologous end joining (NHEJ). In targeted DNA knock-in, donor DNA is copied into the cut site through error-free homologous recombination (HR).
The RepCap plasmid consists of three promoters within the rep coding region that encodes four different Rep proteins. This region also encodes three different VP proteins, the MAAP protein, and the AAP protein.
An AAV with the viral genome inside. This zooms into the the AAV viral genome that is labeled. The viral genome is 4.4 kb maximum, and includes an ITR, promoter, and trangene. Option elements are LoxP sites, WPRE, and pA.

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