| Literature DB >> 26721683 |
Chengzu Long1, Leonela Amoasii1, Alex A Mireault1, John R McAnally1, Hui Li1, Efrain Sanchez-Ortiz1, Samadrita Bhattacharyya1, John M Shelton2, Rhonda Bassel-Duby1, Eric N Olson3.
Abstract
CRISPR/Cas9-mediated genome editing holds clinical potential for treating genetic diseases, such as Duchenne muscular dystrophy (DMD), which is caused by mutations in the dystrophin gene. To correct DMD by skipping mutant dystrophin exons in postnatal muscle tissue in vivo, we used adeno-associated virus-9 (AAV9) to deliver gene-editing components to postnatal mdx mice, a model of DMD. Different modes of AAV9 delivery were systematically tested, including intraperitoneal at postnatal day 1 (P1), intramuscular at P12, and retro-orbital at P18. Each of these methods restored dystrophin protein expression in cardiac and skeletal muscle to varying degrees, and expression increased from 3 to 12 weeks after injection. Postnatal gene editing also enhanced skeletal muscle function, as measured by grip strength tests 4 weeks after injection. This method provides a potential means of correcting mutations responsible for DMD and other monogenic disorders after birth.Entities:
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Year: 2015 PMID: 26721683 PMCID: PMC4760628 DOI: 10.1126/science.aad5725
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728