Author
Listed:
- David G. Ousterout
(Duke University, Room 136 Hudson Hall, Box 90281)
- Ami M. Kabadi
(Duke University, Room 136 Hudson Hall, Box 90281)
- Pratiksha I. Thakore
(Duke University, Room 136 Hudson Hall, Box 90281)
- William H. Majoros
(Program in Computational Biology and Bioinformatics, Duke University)
- Timothy E. Reddy
(Center for Genomic and Computational Biology, Duke University
Duke University Medical Center)
- Charles A. Gersbach
(Duke University, Room 136 Hudson Hall, Box 90281
Center for Genomic and Computational Biology, Duke University
Duke University Medical Center)
Abstract
The CRISPR/Cas9 genome-editing platform is a promising technology to correct the genetic basis of hereditary diseases. The versatility, efficiency and multiplexing capabilities of the CRISPR/Cas9 system enable a variety of otherwise challenging gene correction strategies. Here, we use the CRISPR/Cas9 system to restore the expression of the dystrophin gene in cells carrying dystrophin mutations that cause Duchenne muscular dystrophy (DMD). We design single or multiplexed sgRNAs to restore the dystrophin reading frame by targeting the mutational hotspot at exons 45–55 and introducing shifts within exons or deleting one or more exons. Following gene editing in DMD patient myoblasts, dystrophin expression is restored in vitro. Human dystrophin is also detected in vivo after transplantation of genetically corrected patient cells into immunodeficient mice. Importantly, the unique multiplex gene-editing capabilities of the CRISPR/Cas9 system facilitate the generation of a single large deletion that can correct up to 62% of DMD mutations.
Suggested Citation
David G. Ousterout & Ami M. Kabadi & Pratiksha I. Thakore & William H. Majoros & Timothy E. Reddy & Charles A. Gersbach, 2015.
"Multiplex CRISPR/Cas9-based genome editing for correction of dystrophin mutations that cause Duchenne muscular dystrophy,"
Nature Communications, Nature, vol. 6(1), pages 1-13, May.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7244
DOI: 10.1038/ncomms7244
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