Improved discovery of genetic interactions using CRISPRiSeq across multiple environments.
Mia JaffeAdam DziulkoJustin D SmithRobert P St OngeSasha F LevyGavin SherlockPublished in: Genome research (2019)
Large-scale genetic interaction (GI) screens in yeast have been invaluable for our understanding of molecular systems biology and for characterizing novel gene function. Owing in part to the high costs and long experiment times required, a preponderance of GI data has been generated in a single environmental condition. However, an unknown fraction of GIs may be specific to other conditions. Here, we developed a pooled-growth CRISPRi-based sequencing assay for GIs, CRISPRiSeq, which increases throughput such that GIs can be easily assayed across multiple growth conditions. We assayed the fitness of approximately 17,000 strains encompassing approximately 7700 pairwise interactions in five conditions and found that the additional conditions increased the number of GIs detected nearly threefold over the number detected in rich media alone. In addition, we found that condition-specific GIs are prevalent and improved the power to functionally classify genes. Finally, we found new links during respiratory growth between members of the Ras nutrient-sensing pathway and both the COG complex and a gene of unknown function. Our results highlight the potential of conditional GI screens to improve our understanding of cellular genetic networks.
Keyphrases
- genome wide
- copy number
- dna methylation
- high throughput
- genome wide identification
- physical activity
- escherichia coli
- small molecule
- clinical trial
- body composition
- electronic health record
- transcription factor
- human health
- risk assessment
- randomized controlled trial
- study protocol
- single molecule
- double blind
- deep learning