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Nucleic Acids Res. 2016 Nov 16;44(20):9758-9770. Epub 2016 Aug 11.

A programmable Cas9-serine recombinase fusion protein that operates on DNA sequences in mammalian cells.

Author information

1
Department of Chemistry & Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
2
Howard Hughes Medical institute, Harvard University, Cambridge, MA 02138 USA.
3
Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA 02138, USA.
4
Department of Chemistry & Chemical Biology, Harvard University, Cambridge, MA 02138, USA liu@chemistry.harvard.edu.

Abstract

We describe the development of 'recCas9', an RNA-programmed small serine recombinase that functions in mammalian cells. We fused a catalytically inactive dCas9 to the catalytic domain of Gin recombinase using an optimized fusion architecture. The resulting recCas9 system recombines DNA sites containing a minimal recombinase core site flanked by guide RNA-specified sequences. We show that these recombinases can operate on DNA sites in mammalian cells identical to genomic loci naturally found in the human genome in a manner that is dependent on the guide RNA sequences. DNA sequencing reveals that recCas9 catalyzes guide RNA-dependent recombination in human cells with an efficiency as high as 32% on plasmid substrates. Finally, we demonstrate that recCas9 expressed in human cells can catalyze in situ deletion between two genomic sites. Because recCas9 directly catalyzes recombination, it generates virtually no detectable indels or other stochastic DNA modification products. This work represents a step toward programmable, scarless genome editing in unmodified cells that is independent of endogenous cellular machinery or cell state. Current and future generations of recCas9 may facilitate targeted agricultural breeding, or the study and treatment of human genetic diseases.

PMID:
27515511
PMCID:
PMC5175349
DOI:
10.1093/nar/gkw707
[Indexed for MEDLINE]
Free PMC Article

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