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Nat Biotechnol DOI:10.1038/nbt.2909

Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification.

Publication TypeJournal Article
Year of Publication2014
AuthorsGuilinger, JP, Thompson, DB, Liu, DR
JournalNat Biotechnol
Volume32
Issue6
Pages577-82
Date Published2014 Jun
ISSN1546-1696
KeywordsCaspase 9, Clustered Regularly Interspaced Short Palindromic Repeats, Deoxyribonucleases, Type II Site-Specific, Dimerization, Genome, Humans, Recombinant Fusion Proteins, RNA, RNA Editing
Abstract

Genome editing by Cas9, which cleaves double-stranded DNA at a sequence programmed by a short single-guide RNA (sgRNA), can result in off-target DNA modification that may be detrimental in some applications. To improve DNA cleavage specificity, we generated fusions of catalytically inactive Cas9 and FokI nuclease (fCas9). DNA cleavage by fCas9 requires association of two fCas9 monomers that simultaneously bind target sites ∼15 or 25 base pairs apart. In human cells, fCas9 modified target DNA sites with >140-fold higher specificity than wild-type Cas9 and with an efficiency similar to that of paired Cas9 'nickases', recently engineered variants that cleave only one DNA strand per monomer. The specificity of fCas9 was at least fourfold higher than that of paired nickases at loci with highly similar off-target sites. Target sites that conform to the substrate requirements of fCas9 occur on average every 34 bp in the human genome, suggesting the versatility of this approach for highly specific genome-wide editing.

DOI10.1038/nbt.2909
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/24770324?dopt=Abstract

Alternate JournalNat. Biotechnol.
PubMed ID24770324
PubMed Central IDPMC4263420
Grant List / / Howard Hughes Medical Institute / United States
R01 GM095501 / GM / NIGMS NIH HHS / United States