Mitochondrial DNA editing in potato through mitoTALEN and mitoTALECD: molecular characterization and stability of editing events

• Published in: Plant methods 2024-01, Vol.20 (1), p.4-4, Article 4
• Main Authors: Nicolia, Alessandro, Scotti, Nunzia, D'Agostino, Nunzio, Festa, Giovanna, Sannino, Lorenza, Aufiero, Gaetano, Arimura, Shin-Ichi, Cardi, Teodoro
• Format: Article
• Language: English
• Subjects: Analysis; Base editing; Chondriome; Cytidine deaminase; Editing; Genes; Genetic aspects; Genome editing; Genomes; Genomics; Genotypes; Homologous recombination; Identification and classification; Missense mutation; Mitochondria; Mitochondrial DNA; Mitochondrial DNA editing; MitoTALECD; MitoTALEN; Mutation; Nuclease; Nucleases; Nucleotides; Offspring; Plant mitochondria; Plant propagation; Plants (botany); Plastids; Potatoes; Propagation; Stability
• ISSN: 1746-4811; 1746-4811
• DOI: 10.1186/s13007-023-01124-9

The aim of this study was to evaluate and characterize the mutations induced by two TALE-based approaches, double-strand break (DSB) induction by the FokI nuclease (mitoTALEN) and targeted base editing by the DddA cytidine deaminase (mitoTALECD), to edit, for the first time, the mitochondrial genome of potato, a vegetatively propagated crop. The two methods were used to knock out the same mitochondrial target sequence (orf125). Targeted chondriome deletions of different sizes (236-1066 bp) were induced by mitoTALEN due to DSB repair through ectopic homologous recombination of short direct repeats (11-12 bp) present in the target region. Furthermore, in one case, the induced DSB and subsequent repair resulted in the amplification of an already present substoichiometric molecule showing a 4288 bp deletion spanning the target sequence. With the mitoTALECD approach, both nonsense and missense mutations could be induced by base substitution. The deletions and single nucleotide mutations were either homoplasmic or heteroplasmic. The former were stably inherited in vegetative offspring. Both editing approaches allowed us to obtain plants with precisely modified mitochondrial genomes at high frequency. The use of the same plant genotype and mtDNA region allowed us to compare the two methods for efficiency, accuracy, type of modifications induced and stability after vegetative propagation.