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Tools for editing the mammalian mitochondrial genome.

Carlos Torres Moraes
Published in: Human molecular genetics (2024)
The manipulation of animal mitochondrial genomes has long been a challenge due to the lack of an effective transformation method. With the discovery of specific gene editing enzymes, designed to target pathogenic mitochondrial DNA mutations (often heteroplasmic), the selective removal or modification of mutant variants has become a reality. Because mitochondria cannot efficiently import RNAs, CRISPR has not been the first choice for editing mitochondrial genes. However, the last few years witnessed an explosion in novel and optimized non-CRISPR approaches to promote double-strand breaks or base-edit of mtDNA in vivo. Engineered forms of specific nucleases and cytidine/adenine deaminases form the basis for these techniques. I will review the newest developments that constitute the current toolbox for animal mtDNA gene editing in vivo, bringing these approaches not only to the exploration of mitochondrial function, but also closer to clinical use.
Keyphrases
  • mitochondrial dna
  • copy number
  • crispr cas
  • genome wide
  • genome editing
  • oxidative stress
  • dna methylation
  • small molecule
  • cell death
  • high throughput
  • gene expression
  • reactive oxygen species