Cas9/gRNA-mediated genome editing of yeast mitochondria and Chlamydomonas chloroplasts

• Published in: PeerJ (San Francisco, CA) Vol. 8; p. e8362
• Main Authors: Yoo, Byung-Chun, Yadav, Narendra S, Orozco, Jr, Emil M, Sakai, Hajime
• Format: Journal Article
• Language: English
• Published: United States PeerJ, Inc 06.01.2020; PeerJ Inc
• Subjects: Bioengineering; Biotechnology; Cas9/gRNA; Chlamydomonas; Chloroplast; Chloroplasts; CRISPR; Deoxyribonucleic acid; Design; DNA; DNA repair; Gene expression; Gene therapy; Genetic engineering; Genetics; Genome editing; Genomes; Genomics; gRNA; Homologous recombination; Integration; Metabolites; Mitochondria; Non-homologous end joining; Organelle; Organelles; Plasmids; Promoters; Proteins; Ribonucleic acid; RNA; Synthetic Biology; CRISPR; Mitochondria; Yeast; Organelle; Genome editing; Cas9/gRNA; DNA replacement; Edit Plasmid; Chlamydomonas; Chloroplast
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.8362

We present a new approach to edit both mitochondrial and chloroplast genomes. Organelles have been considered off-limits to CRISPR due to their impermeability to most RNA and DNA. This has prevented applications of Cas9/gRNA-mediated genome editing in organelles while the tool has been widely used for engineering of nuclear DNA in a number of organisms in the last several years. To overcome the hurdle, we designed a new approach to enable organelle genome editing. The plasmids, designated "Edit Plasmids," were constructed with two expression cassettes, one for the expression of Cas9, codon-optimized for each organelle, under promoters specific to each organelle, and the other cassette for the expression of guide RNAs under another set of promoters specific to each organelle. In addition, Edit Plasmids were designed to carry the donor DNA for integration between two double-strand break sites induced by Cas9/gRNAs. Each donor DNA was flanked by the regions homologous to both ends of the integration site that were short enough to minimize spontaneous recombination events. Furthermore, the donor DNA was so modified that it did not carry functional gRNA target sites, allowing the stability of the integrated DNA without being excised by further Cas9/gRNAs activity. Edit Plasmids were introduced into organelles through microprojectile transformation. We confirmed donor DNA insertion at the target sites facilitated by homologous recombination only in the presence of Cas9/gRNA activity in yeast mitochondria and chloroplasts. We also showed that Edit Plasmids persist and replicate in mitochondria autonomously for several dozens of generations in the presence of the wild-type genomes. Finally, we did not find insertions and/or deletions at one of the Cas9 cleavage sites in Chloroplasts, which are otherwise hallmarks of Cas9/gRNA-mediated non-homologous end joining (NHEJ) repair events in nuclear DNA. This is consistent with previous reports of the lack of NHEJ repair system in most bacteria, which are believed to be ancestors of organelles. This is the first demonstration of CRISPR-mediated genome editing in both mitochondria and chloroplasts in two distantly related organisms. The Edit Plasmid approach is expected to open the door to engineer organelle genomes of a wide range of organisms in a precise fashion.