Figure 1.
A CRISPR screen reveals PD-L1 regulating genes. (A) Cell surface expression of PD-L1 in ATLL cell lines, ALK+ ALCL cell lines, and T-ALL cell lines measured by flow cytometry. (B) Schematic design of the CRISPR library screen in the study. Two Cas9-transducing ATLL cell lines, ST1 and KK1, were used for identifying genes whose knockout decreases or increases PD-L1 expression, respectively. (C) Log2 fold-changes (sorted/unsorted population) of genes enriched in ST1 expressing low level PD-L1 (left panel) and in KK1 expressing high level PD-L1 (right panel). (D) Top 10 log2 fold change genes with 3 or 4 sgRNA log2 fold changes ≥1.0 in ST1 expressing low level PD-L1 (left panel) and in KK1 expressing high level PD-L1 (right panel).

A CRISPR screen reveals PD-L1 regulating genes. (A) Cell surface expression of PD-L1 in ATLL cell lines, ALK+ ALCL cell lines, and T-ALL cell lines measured by flow cytometry. (B) Schematic design of the CRISPR library screen in the study. Two Cas9-transducing ATLL cell lines, ST1 and KK1, were used for identifying genes whose knockout decreases or increases PD-L1 expression, respectively. (C) Log2 fold-changes (sorted/unsorted population) of genes enriched in ST1 expressing low level PD-L1 (left panel) and in KK1 expressing high level PD-L1 (right panel). (D) Top 10 log2 fold change genes with 3 or 4 sgRNA log2 fold changes ≥1.0 in ST1 expressing low level PD-L1 (left panel) and in KK1 expressing high level PD-L1 (right panel).

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