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- W2892631154 endingPage "327" @default.
- W2892631154 startingPage "307" @default.
- W2892631154 abstract "The ease of performing both forward and reverse genetics in Saccharomyces cerevisiae, along with its stable haploid state and short generation times, has made this budding yeast the consummate model eukaryote for genetics. The major advantage of using budding yeast for reverse genetics is this organism’s highly efficient homology-directed repair, allowing for precise genome editing simply by introducing DNA with homology to the chromosomal target. Although plasmid- and PCR-based genome editing tools are quite efficient, they depend on rare spontaneous DNA breaks near the target sequence. Consequently, they can generate only one genomic edit at a time, and the edit must be associated with a selectable marker. However, CRISPR/Cas technology is efficient enough to permit markerless and multiplexed edits in a single step. These features have made CRISPR/Cas popular for yeast strain engineering in synthetic biology and metabolic engineering applications, but it has not been widely employed for genetic screens. In this review, we critically examine different methods to generate multi-mutant strains in systematic genetic interaction screens and discuss the potential of CRISPR/Cas to supplement or improve on these methods." @default.
- W2892631154 created "2018-10-05" @default.
- W2892631154 creator A5003263037 @default.
- W2892631154 creator A5016548828 @default.
- W2892631154 creator A5086336387 @default.
- W2892631154 date "2018-09-25" @default.
- W2892631154 modified "2023-10-16" @default.
- W2892631154 title "Yeast genetic interaction screens in the age of CRISPR/Cas" @default.
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