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Germline CRISPR/Cas9-mediated Gene Editing Prevents Vision Loss in a Novel Mouse Model of Aniridia

Mol Ther Methods Clin Dev. 2020; 
Seyedeh Zeinab Mirjalili Mohanna,  Jack W. Hickmott, Siu Ling Lam,  Nina Y. Chiu,  Tess C. Lengyell,  Beatrice M. Tam, Orson L. Moritz,  and Elizabeth M. Simpson
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CRISPR Plasmids The commercially synthesized CRISPR RNA (crRNA) and trans-activating crRNA (tracrRNA) (GenScript, Piscataway, NJ, USA) were annealed at a 1:1 ratio by incubating at 95°C for 5 min to generate gRNA.  Get A Quote

摘要

Aniridia is a rare eye disorder, which is caused by mutations in the paired box 6 (PAX6) gene and results in vision loss due to the lack of a long-term vision-saving therapy. One potential approach to treating aniridia is targeted CRISPR-based genome editing. To enable the Pax6 small eye (Sey) mouse model of aniridia, which carries the same mutation found in patients, for preclinical testing of CRISPR-based therapeutic approaches, we endogenously tagged the Sey allele, allowing for the differential detection of protein from each allele. We optimized a correction strategy in vitro then tested it in vivo in the germline of our new mouse to validate the causality of the Sey mutation. The genomic manipu... More

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