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Nat Commun. 2017 Feb 21;8:14500. doi: 10.1038/ncomms14500.

In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni.

Kim E1,2, Koo T1,3, Park SW4,5, Kim D1,6, Kim K1, Cho HY1, Song DW2, Lee KJ2, Jung MH2, Kim S2, Kim JH4,5, Kim JH4,5,7, Kim JS1,3,6.

Author information

1
Center for Genome Engineering, Institute for Basic Science (IBS), Seoul 08826, Republic of Korea.
2
ToolGen, Byucksan Digital Valley 6-cha, 219 Gasan Digital 1-ro, Geumcheon-gu, Seoul 08501, Republic of Korea.
3
Department of Functional Genomics, University of Science and Technology, Daejeon 34113, Republic of Korea.
4
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
5
FARB Laboratory, Biomedical Research Institute, Seoul National University Hospital, Seoul 03082, Republic of Korea.
6
Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
7
Department of Ophthalmology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Abstract

Several CRISPR-Cas9 orthologues have been used for genome editing. Here, we present the smallest Cas9 orthologue characterized to date, derived from Campylobacter jejuni (CjCas9), for efficient genome editing in vivo. After determining protospacer-adjacent motif (PAM) sequences and optimizing single-guide RNA (sgRNA) length, we package the CjCas9 gene, its sgRNA sequence, and a marker gene in an all-in-one adeno-associated virus (AAV) vector and produce the resulting virus at a high titer. CjCas9 is highly specific, cleaving only a limited number of sites in the human or mouse genome. CjCas9, delivered via AAV, induces targeted mutations at high frequencies in mouse muscle cells or retinal pigment epithelium (RPE) cells. Furthermore, CjCas9 targeted to the Vegfa or Hif1a gene in RPE cells reduces the size of laser-induced choroidal neovascularization, suggesting that in vivo genome editing with CjCas9 is a new option for the treatment of age-related macular degeneration.

PMID:
28220790
PMCID:
PMC5473640
DOI:
10.1038/ncomms14500
[Indexed for MEDLINE]
Free PMC Article

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