Gene Editing and Protein Tagging in the Oomycete Phytophthora infestans Using CRISPR-Cas12a
- PMID: 39729268
- DOI: 10.1007/978-1-0716-4330-3_4
Gene Editing and Protein Tagging in the Oomycete Phytophthora infestans Using CRISPR-Cas12a
Abstract
Molecular genetic tools such as CRISPR-Cas gene editing systems are invaluable for understanding gene and protein function and revealing the details of a pathogen's life and disease cycles. Here we present protocols for genome editing in Phytophthora infestans, an oomycete with global importance as a pathogen of potato and tomato. Using a vector system that expresses variants of Cas12a from Lachnospiraceae bacterium and its guide RNA from a unified transcript, we first present a method for editing genes through the non-homologous end-joining (NHEJ) pathway. We then describe an application of homology-directed repair (HDR), in which Cas12a is used to fuse a protein-coding gene with a fluorescent or epitope tag. Both methods should be adaptable to many oomycetes other than P. infestans.
Keywords: CRISPR; Fluorescent reporter; Gene editing; Oomycete; Transformation.
© 2025. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
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