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Efficient elimination of MELAS-associated m.3243G mutant mitochondrial DNA by an engineered mitoARCUS nuclease.
Shoop, Wendy K; Lape, Janel; Trum, Megan; Powell, Alea; Sevigny, Emma; Mischler, Adam; Bacman, Sandra R; Fontanesi, Flavia; Smith, Jeff; Jantz, Derek; Gorsuch, Cassandra L; Moraes, Carlos T.
Afiliación
  • Shoop WK; Precision BioSciences, Durham, NC, USA.
  • Lape J; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Trum M; Precision BioSciences, Durham, NC, USA.
  • Powell A; Precision BioSciences, Durham, NC, USA.
  • Sevigny E; Precision BioSciences, Durham, NC, USA.
  • Mischler A; Precision BioSciences, Durham, NC, USA.
  • Bacman SR; Precision BioSciences, Durham, NC, USA.
  • Fontanesi F; Department of Neurology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Smith J; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Jantz D; Precision BioSciences, Durham, NC, USA.
  • Gorsuch CL; Precision BioSciences, Durham, NC, USA.
  • Moraes CT; Precision BioSciences, Durham, NC, USA. cassie.gorsuch@precisionbiosciences.com.
Nat Metab ; 5(12): 2169-2183, 2023 Dec.
Article en En | MEDLINE | ID: mdl-38036771
Nuclease-mediated editing of heteroplasmic mitochondrial DNA (mtDNA) seeks to preferentially cleave and eliminate mutant mtDNA, leaving wild-type genomes to repopulate the cell and shift mtDNA heteroplasmy. Various technologies are available, but many suffer from limitations based on size and/or specificity. The use of ARCUS nucleases, derived from naturally occurring I-CreI, avoids these pitfalls due to their small size, single-component protein structure and high specificity resulting from a robust protein-engineering process. Here we describe the development of a mitochondrial-targeted ARCUS (mitoARCUS) nuclease designed to target one of the most common pathogenic mtDNA mutations, m.3243A>G. mitoARCUS robustly eliminated mutant mtDNA without cutting wild-type mtDNA, allowing for shifts in heteroplasmy and concomitant improvements in mitochondrial protein steady-state levels and respiration. In vivo efficacy was demonstrated using a m.3243A>G xenograft mouse model with mitoARCUS delivered systemically by adeno-associated virus. Together, these data support the development of mitoARCUS as an in vivo gene-editing therapeutic for m.3243A>G-associated diseases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Síndrome MELAS Límite: Animals / Humans Idioma: En Revista: Nat Metab Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Síndrome MELAS Límite: Animals / Humans Idioma: En Revista: Nat Metab Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos