Skip to main content
. 2022 Oct 10;20(10):e3001543. doi: 10.1371/journal.pbio.3001543

Fig 2. Validation of selected genes identified in the CRISPR-Cas9 screen.

Fig 2

(A) Main functional groups derived from genes recovered in the screen. Genes selected for further validation are shaded in grey. (B) Representative immunofluorescence flow cytometry assays and immunoblots after siRNA-mediated depletion of selected genes. Cells transfected with nontargeting (siNT) or gene-specific siRNAs were mock- or UV-treated (1 J/m2). % RPAhigh cells (dashed box) were assessed 6 h after irradiation. (C) Quantification of (B). Values represent the mean ± SEM of at least 3 independent experiments. Statistics used: unpaired t test corrected for multiple comparisons using the Holm–Šídák method. *: p ≤ 0.05, **: p ≤ 0.01, ***: p ≤ 0.001, ****: p ≤ 0.0001. The data underlying the graph shown in the figure can be found in S1 Data. a.u., arbitrary units; RPA, Replication Protein A.