Mendoza Carl S, Ah-Fong Audrey M V, Judelson Howard S
Department of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.
Methods Mol Biol. 2025;2892:49-67. doi: 10.1007/978-1-0716-4330-3_4.
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.
诸如CRISPR-Cas基因编辑系统等分子遗传学工具对于理解基因和蛋白质功能以及揭示病原体的生命和疾病周期细节非常重要。在此,我们展示了针对致病疫霉(Phytophthora infestans)基因组编辑的方案,致病疫霉作为马铃薯和番茄的病原体,在全球范围内具有重要意义。我们使用一种载体系统,该系统从毛螺菌科细菌中表达Cas12a变体及其来自统一转录本的引导RNA,首先展示了一种通过非同源末端连接(NHEJ)途径编辑基因的方法。然后,我们描述了同源定向修复(HDR)的应用,其中Cas12a用于将蛋白质编码基因与荧光或表位标签融合。这两种方法应该都适用于除致病疫霉之外的许多卵菌。