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

Extended Data Fig. 2. XRCC1 promotes the recovery of transcription following oxidative damage.

Extended Data Fig. 2

a, Representative images of the RNAPI foci (RPA194) and levels of global transcription (EU immunofluorescence) in WT and XRCC1−/− U2OS cells stably transfected with either empty vector (EV) or expression construct encoding full length C-terminal histidine-tagged XRCC1 (XRCC1WT), following mock treatment or at the indicated times after treatment with 1 mM H2O2 for 20 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, Immunoblot of RNAPII hyperphosphorylation in WT U2OS cells, XRCC1−/− U2OS cells, and XRCC1−/− U2OS cells stably transfected with either empty vector (EV) or expression construct encoding full-length histidine-tagged XRCC1 (XRCC1WT), following mock treatment or 2 h after treatment with 1 mM H2O2 for 20 min. A representative blot from one of three independent experiments is shown.

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