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. 2021 Nov 22;23(12):1287–1298. doi: 10.1038/s41556-021-00792-w

Extended Data Fig. 3. Reduced transcriptional recovery in XRCC1-deficient cells is a result of toxic PARP1 activity.

Extended Data Fig. 3

a, Representative images of the RNAPI foci (RPA194 immunofluorescence) and levels of global transcription (EU immunofluorescence) in WT and XRCC1−/− RPE-1 cells pretreated with PARP1 inhibitor (PARPi) following mock treatment or at the indicated times after treatment with 250 μM H2O2 for 5 min. Scale bars, 10 μm. b and c, Quantification of the RNAPI foci (RPA194) and levels of global transcription (EU immunofluorescence) shown in (a). Data are means (±s.e.m.) of three independent experiments, and statistically significant differences were determined by two-way ANOVA with Tukey’s multiple comparisons test (p values are indicated). d, Representative images of the RNAPI foci (RPA194) and levels of global transcription (EU immunofluorescence) in WT and XRCC1−/− U2OS cells pretreated with PARP1 inhibitor (PARPi) following mock treatment or at the indicated times after treatment with 1 mM H2O2 for 20 min. Scale bars, 10 μm. e and f, Quantification of the RNAPI foci (RPA194) and levels of global transcription (EU immunofluorescence) shown in (d). Data are means (±s.e.m.) of three independent experiments, and statistically significant differences were determined by two-way ANOVA with Tukey’s multiple comparisons test (p values are indicated).

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