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. Author manuscript; available in PMC: 2020 Nov 20.
Published in final edited form as: Nat Chem Biol. 2019 Apr 15;15(5):529–539. doi: 10.1038/s41589-019-0263-0

Fig. 1 |. CRISPR-suppressor scanning identifies regions of LSD1 that mediate its function and susceptibility to pharmacological inhibitors.

Fig. 1 |

a, Schematic of CRISPR-suppressor scanning workflow to profile SARs of LSD1 small-molecule inhibitors. b, Heat maps depicting log2(fold-change sgRNA enrichment) in SET-2 at the indicated time points and conditions versus week 0 normalized against functionally neutral genome-targeting control sgRNAs. The sgRNAs are arrayed on the x axis by the LSD1 CDS. Color represents mean values across three replicate transductions. c, Scatter plot showing log2(fold-change sgRNA enrichment) in SET-2 under GSK-LSD1 treatment at week 8 versus week 0 normalized against functionally neutral genome-targeting control sgRNAs. The sgRNAs are arrayed on the x axis by the LSD1 CDS. Data represent mean values across three replicate transductions. d, Heat map showing cross-correlation of overall sgRNA enrichment at the specified time points during the CRISPR-suppressor scanning in SET-2. Data represent mean values across three replicate transductions.