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Targeted Gene Editing in Porcine Germ Cells.
Goldsmith, Taylor; Bondareva, Alla; Webster, Dennis; Voigt, Anna Laura; Su, Lin; Carlson, Daniel F; Dobrinski, Ina.
Affiliation
  • Goldsmith T; Recombinetics, Inc., St. Paul, MN, USA.
  • Bondareva A; Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Webster D; Recombinetics, Inc., St. Paul, MN, USA.
  • Voigt AL; Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Su L; Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Carlson DF; Recombinetics, Inc., St. Paul, MN, USA.
  • Dobrinski I; Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. idobrins@ucalgary.ca.
Methods Mol Biol ; 2495: 245-258, 2022.
Article de En | MEDLINE | ID: mdl-35696037
ABSTRACT
As the genetic mutations driving human disease are identified, there is an increasing need for a biomedical model that can accurately represent the disease of interest and provide a platform for potential therapeutic testing. Pigs are a better model for human disease than rodents because of their genetic and physiological similarities to humans. However, current methods to generate porcine models are both technically challenging and expensive. Germline genetic modification through gene edited spermatogonia provides an effective alternative to how these models are developed. Here, we report an improved technique of gene editing in spermatogonia of pigs using CRISPR-Cas9 to generate different edits that reflect the genotypes of human diseases.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Systèmes CRISPR-Cas / Édition de gène Limites: Animals Langue: En Journal: Methods Mol Biol Sujet du journal: BIOLOGIA MOLECULAR Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Systèmes CRISPR-Cas / Édition de gène Limites: Animals Langue: En Journal: Methods Mol Biol Sujet du journal: BIOLOGIA MOLECULAR Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique