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Generation of a Human Deafness Sheep Model Using the CRISPR/Cas System.
Crispo, Martina; Chenouard, Vanessa; Dos Santos-Neto, Pedro; Tesson, Laurent; Souza-Neves, Marcela; Heslan, Jean-Marie; Cuadro, Federico; Anegón, Ignacio; Menchaca, Alejo.
Afiliación
  • Crispo M; Laboratory Animal Biotechnology Unit, Institut Pasteur de Montevideo, Montevideo, Uruguay.
  • Chenouard V; INSERM Centre de Recherche en Transplantation et Immunologie UMR 1064, Transgenesis Rat ImmunoPhenomic Facility (TRIP), Nantes, France.
  • Dos Santos-Neto P; Instituto de Reproducción Animal Uruguay, Fundación IRAUy, Montevideo, Uruguay.
  • Tesson L; INSERM Centre de Recherche en Transplantation et Immunologie UMR 1064, Transgenesis Rat ImmunoPhenomic Facility (TRIP), Nantes, France.
  • Souza-Neves M; Instituto de Reproducción Animal Uruguay, Fundación IRAUy, Montevideo, Uruguay.
  • Heslan JM; INSERM Centre de Recherche en Transplantation et Immunologie UMR 1064, Transgenesis Rat ImmunoPhenomic Facility (TRIP), Nantes, France.
  • Cuadro F; Instituto de Reproducción Animal Uruguay, Fundación IRAUy, Montevideo, Uruguay.
  • Anegón I; INSERM Centre de Recherche en Transplantation et Immunologie UMR 1064, Transgenesis Rat ImmunoPhenomic Facility (TRIP), Nantes, France.
  • Menchaca A; Instituto de Reproducción Animal Uruguay, Fundación IRAUy, Montevideo, Uruguay. menchaca.alejo@gmail.com.
Methods Mol Biol ; 2495: 233-244, 2022.
Article en En | MEDLINE | ID: mdl-35696036
ABSTRACT
CRISPR/Cas9 system is a promising method for the generation of human disease models by genome editing in non-conventional experimental animals. Medium/large-sized animals like sheep have several advantages to study human diseases and medicine. Here, we present a protocol that describes the generation of an otoferlin edited sheep model via CRISPR-assisted single-stranded oligodinucleotide-mediated Homology-Directed Repair (HDR), through direct cytoplasmic microinjection in in vitro produced zygotes.Otoferlin is a protein expressed in the cochlear inner hair cells, with different mutations at the OTOF gene being the major cause of nonsyndromic recessive auditory neuropathy spectrum disorder in humans. By using this protocol, we reported for the first time an OTOF KI model in sheep with 17.8% edited lambs showing indel mutations, and 61.5% of them bearing knock-in mutations by HDR . The reported method establishes the bases to produce a deafness model to test novel therapies in human disorders related to OTOF mutations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sordera / Sistemas CRISPR-Cas Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Uruguay

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sordera / Sistemas CRISPR-Cas Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Uruguay