Mitochondrial targeted meganuclease as a platform to eliminate mutant mtDNA in vivo

Nat Commun. 2021 May 28;12(1):3210. doi: 10.1038/s41467-021-23561-7.

Abstract

Diseases caused by heteroplasmic mitochondrial DNA mutations have no effective treatment or cure. In recent years, DNA editing enzymes were tested as tools to eliminate mutant mtDNA in heteroplasmic cells and tissues. Mitochondrial-targeted restriction endonucleases, ZFNs, and TALENs have been successful in shifting mtDNA heteroplasmy, but they all have drawbacks as gene therapy reagents, including: large size, heterodimeric nature, inability to distinguish single base changes, or low flexibility and effectiveness. Here we report the adaptation of a gene editing platform based on the I-CreI meganuclease known as ARCUS®. These mitochondrial-targeted meganucleases (mitoARCUS) have a relatively small size, are monomeric, and can recognize sequences differing by as little as one base pair. We show the development of a mitoARCUS specific for the mouse m.5024C>T mutation in the mt-tRNAAla gene and its delivery to mice intravenously using AAV9 as a vector. Liver and skeletal muscle show robust elimination of mutant mtDNA with concomitant restoration of mt-tRNAAla levels. We conclude that mitoARCUS is a potential powerful tool for the elimination of mutant mtDNA.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA Restriction Enzymes / genetics
  • DNA Restriction Enzymes / metabolism*
  • DNA, Mitochondrial / genetics
  • DNA, Mitochondrial / metabolism*
  • Dependovirus / genetics
  • Disease Models, Animal
  • Fibroblasts
  • Gene Editing / methods
  • Genetic Therapy / methods*
  • Genetic Vectors / administration & dosage*
  • Genetic Vectors / genetics
  • HeLa Cells
  • Humans
  • Mice
  • Mice, Transgenic
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / therapy*
  • Point Mutation
  • Primary Cell Culture
  • RNA, Transfer, Ala / genetics

Substances

  • DNA, Mitochondrial
  • RNA, Transfer, Ala
  • DNA Restriction Enzymes
  • endodeoxyribonuclease CreI