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. 2023 Nov 15;14:7384. doi: 10.1038/s41467-023-42390-4

Fig. 1. RNAP1 and FBL localization during DNA repair in SMN deficient transformed fibroblasts.

Fig. 1

a Representative confocal microscopy images of immunofluorescence (IF) assay in MRC5 cells showing, after 16 J/m² UV-C irradiation, the localization of RNAP1 (green) and FBL (red) in transformed fibroblasts, at different times Post UV-Irradiation (PUVI). Nuclei and nucleoli are indicated by dashed and dotted lines respectively. Scale bar: 5 µm. b Quantification of cell number for RNAP1 localization (inside the nucleolus, outside the nucleolus or mixed localization) at different times PUVI. At least 50 cells from one representative experiment were analyzed. c Western Blot of SMN and CSB on whole cell extracts of transformed fibroblasts (MRC5-SV cells). Doxycycline treatment induces the expression of the ShRNA against SMN. d Quantification of RNA-FISH assay showing the 47 S pre-rRNA level after UV-C exposure in transformed fibroblasts. Data are represented as mean values +/− SEM. At least 27 cells was quantified from one representative experiment. The p-value correspond to a student’s test with two-tailed distribution and two-sample unequal variance to compare after irradiation with No UV condition. Source data of uncropped gel and graphs are provided as a Source Data file.