Adenovirus Vector‐Mediated In Vivo Knock‐in Treatment of Neonatal Phenylketonuria Mice Using Terminally Cleaved Donor DNA
Megumi Yamaji, Hirotaka Tabata, Mariko Nakamura, Ryoko Fuse, Tadashi Okada, Shun‐Ichi Ohba, Tomokazu Ohishi, Manabu Kawada, Izumu Saito, Shigeto Sato, Tomoko NakanishiABSTRACT
Background
Adenovirus vectors (AdVs) are widely used and have an advantage of large insert capacity compared with adeno‐associated virus vectors. However, AdVs have scarcely been used in genome‐editing knock‐in strategies because of low efficiency.
Methods
Novel AdVs possessing a very large, 3.7 kb donor DNA fragment and six or eight multiplex gRNA expression units were developed for CRISPR/Cas9‐mediated knock‐in to correct a phenylalanine hydroxylase ( Pah ) gene in a Pah enu2 phenylketonuria mouse model. These AdVs were co‐infected to Hepa1–6 cells or liver cells in vivo together with an AdV expressing either native Cas9 or Cas9 nickase (Cas9n) for double‐nicking cleavage.
Results
In vitro knock‐in of the AdVs carrying 3.7 kb donor DNA and six gRNA units targeting the cell genome was observed in both cases using Cas9 and Cas9n, though their efficiencies were low. Therefore, we generated AdVs carrying an additional two gRNA units that cleave the donor DNA terminus in the AdV genome via native Cas9 or Cas9 nickase. The knock‐in efficiency increased approximately twofold for both vectors and reached a maximum of 8% for native Cas9 without selection. Newborn phenylketonuria model mice were intravenously administered the knock‐in AdV together with the native‐Cas9 AdV. Although the knock‐in efficiency by homologous recombination occurred in only approximately 1% of hepatocytes, blood phenylalanine levels were reduced by up to 30%. Also, unintended fragments produced by nonhomologous end‐joining were observed between the cleavage site at the terminus of the donor DNA in the AdV genome and the target site in the cell genome.
Conclusions
The knock‐in efficiency of AdVs can be increased by cleaving the terminus of the donor DNA, although it would be desirable to avoid nonhomologous end‐joining between double‐strand break termini.