A pipeline for precise and efficient genome editing by sgRNA-Cas9 RNPs in Drosophila

• Published in: Fly (Austin, Tex.) Vol. 14; no. 1-4; pp. 34 - 48
• Main Authors: Nyberg, Kevin G, Nguyen, Joseph Q, Kwon, Yong-Jae, Blythe, Shelby, Beitel, Greg J, Carthew, Richard
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01.10.2020; Taylor & Francis Group
• Subjects: Animals; Chromosomes; crispr; CRISPR-Associated Protein 9 - metabolism; drosophila; Drosophila melanogaster - embryology; Drosophila melanogaster - genetics; gene editing; Gene Editing - methods; homology dependent repair; Methods and Technical Advances; Ribonucleoproteins - genetics; Ribonucleoproteins - metabolism; RNA, Guide, CRISPR-Cas Systems - genetics; RNA, Guide, CRISPR-Cas Systems - metabolism; CRISPR; homology dependent repair; gene editing; Drosophila
• ISSN: 1933-6934; 1933-6942
• DOI: 10.1080/19336934.2020.1832416

Genome editing via homology-directed repair (HDR) has made possible precise and deliberate modifications to gene sequences. CRISPR/Cas9-mediated HDR is the simplest means to carry this out. However, technical challenges remain to improve efficiency and broaden applicability to any genetic background of as well as to other species. To address these issues, we developed a two-stage marker-assisted strategy in which embryos are injected with RNPs and pre-screened using T7EI. Using sgRNA in complex with recombinant Cas9 protein, we assayed each sgRNA for genome-cutting efficiency. We then conducted HDR using sgRNAs that efficiently cut target genes and the application of a transformation marker that generates RNAi against . This allows for screening based on eye morphology rather than colour. These new tools can be used to make a single change or a series of allelic substitutions in a region of interest, or to create additional genetic tools such as balancer chromosomes.