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. 2020 May 19;11:2506. doi: 10.1038/s41467-020-16052-8

Fig. 6. Downstream effects on aberrant splicing on ESRRG.

Fig. 6

a The qRT-PCR results display ESRRG mRNA expression levels in primary human prolactinoma cells transfected with control or specific ESRRG siRNA. GAPDH was used as an internal control (n = 3 per group). b Suppression of PRL secretion in primary human prolactinomas cells after ESRRG knockdown using ESRRG siRNA (n = 9 per group). c Results of CCK-8 cell proliferation assay in GH3 cells infected with Ad-null, Ad-canonical ESRRG, and Ad-cryptic ESRRG (n = 5 per group). d Results of CCK-8 cell proliferation assay in MMQ cells infected with Ad-null, Ad-canonical ESRRG, and Ad-cryptic ESRRG (n = 5 per group). e Focus formation was assessed in GH3 cells infected with Ad-null, Ad-canonical ESRRG and Ad-cryptic ESRRG (n = 9 per group). f Focus formations were assessed in MMQ cells infected with Ad-null, Ad-canonical ESRRG, and Ad-cryptic ESRRG (n = 9 per group). g Annexin V/PI staining and flow cytometry showed the percentages of apoptosis of the GH3 cells infected with Ad-null, Ad-canonical ESRRG, and Ad-cryptic ESRRG (n = 9 per group). h Annexin V/PI staining and flow cytometry showed the percentages of apoptosis of the MMQ cells infected with Ad-null, Ad-canonical ESRRG, and Ad-cryptic ESRRG (n = 9 per group). Results are expressed as mean ± SD. The p values by one-way ANOVA followed by Dunnett’s multiple comparisons test in a, b and followed by Tukey’s multiple comparisons post hoc test in ch are indicated. Source data are provided as a Source Data file.