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. 2020 Mar 1;34(5-6):413–427. doi: 10.1101/gad.332270.119

Figure 4.

Figure 4.

The NMD-inducing activity of SRSF2 is dependent on the EJC. (A) Western blotting of HeLa cells treated with the indicated siRNAs. Tubulin was used as a loading control. (B) Quantification of knockdown efficiency in A, relative to control siRNA against luciferase (%) (mean ± SD, n = 3). (C) Radioactive RT-PCR of the HBB reporters (WT or T39) of the indicated siRNA-treated HeLa cells cotransfected with the indicated cDNAs. (#) An intron 1 retained transcript variant. (D) mRNA bands in C were quantified, normalized to GFP, and plotted as T39/WT (%) (mean ± SD, n = 3). (*) P < 0.05; (**) P < 0.01; (***) P < 0.001, compared with corresponding empty vector-treated cells, t-test.