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. 2020 Jun 15;9(6):60. doi: 10.1038/s41389-020-00244-4

Fig. 1. A focused screen identified transcription-related nuclear speckle factors as HR regulators.

Fig. 1

a U2OS cells treated with tubercidin or mock treated (dimethyl sulfoxide: DMSO) were subjected to immunofluorescence staining with the anti-SC35 antibody. Scale bar: 10 μm. b U2OS cells were incubated with tubercidin or DMSO followed by treatment with CPT. Cell extracts were subjected to immunoblotting analysis with the indicated antibodies. c Screen for nuclear speckle factors involved in HR regulation. The DR-GFP assay was performed with siRNA pools targeting nuclear speckle factors. The siRNA targeting CtIP or luciferase (control: Ctrl) was used as a positive or negative control, respectively, and indicated with blue markers. Homology directed repair efficiency is plotted as a Z-score. The inset magnifies the data for top hits with gene symbols. The genes previously reported to be involved in HR regulation are indicated with green. d A DR-GFP assay was carried out with two independent siRNAs targeting selected top hits from the initial screen. GFP-positive cell populations were normalized to mock treatment (Ctrl), which was set to 100% (mean ± SEM, n = 3). *p < 0.05. **p < 0.01. ***p < 0.005.