Journal
GENETICS
Volume 208, Issue 4, Pages 1357-1372Publisher
OXFORD UNIV PRESS INC
DOI: 10.1534/genetics.117.300656
Keywords
Cryptococcus neoformans; electroporation; biolistic transformation; CRISPR-Cas9; gene disruption; gene complementation; ectopic integration; double-strand break; gene family
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Funding
- Investigator Award in the Pathogenesis of Infectious Disease from the Burroughs Wellcome Fund [1012445]
- National Institutes of Health [R01AI097599]
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Cryptococcus neoformans is a fungal pathogen that claims hundreds of thousands of lives annually. Targeted genetic manipulation through biolistic transformation in C. neoformans drove the investigation of this clinically important pathogen at the molecular level. Although costly and inefficient, biolistic transformation remains the major method for editing the Cryptococcus genome as foreign DNAs introduced by other methods such as electroporation are predominantly not integrated into the genome. Although the majority of DNAs introduced by biolistic transformation are stably inherited, the transformation efficiency and the homologous integration rate (similar to 1-10%) are low. Here, we developed a Transient CRISPR (clustered regularly interspaced short palindromic repeat)-Cas9 coupled with Electroporation (TRACE) system for targeted genetic manipulations in the C. neoformans species complex. This method took advantages of efficient genome integration due to double-strand breaks created at specific sites by the transient CRISPR-Cas9 system and the high transformation efficiency of electroporation. We demonstrated that TRACE can efficiently generate precise single-gene deletion mutants using the ADE2 locus as an example. This system can also effectively delete multiple genes in a single transformation, as evident by the successful generation of quadruple mf alpha 1 Delta 2 Delta 3 Delta 4 Delta mutants. In addition to generating gene deletion mutants, we complemented the ade2 Delta mutant by integrating a wild-type ADE2 allele at the safe haven region (SH2) via homologous recombination using TRACE. Interestingly, introduced DNAs can be inserted at a designated genetic site without any homologous sequences, opening up numerous other applications. We expect that TRACE, an efficient, versatile, and cost-effective gene editing approach, will greatly accelerate research in this field.
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