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©The Author(s) 2018.
World J Gastroenterol. Dec 7, 2018; 24(45): 5120-5130
Published online Dec 7, 2018. doi: 10.3748/wjg.v24.i45.5120
Published online Dec 7, 2018. doi: 10.3748/wjg.v24.i45.5120
Figure 3 Prediction of the transcription factors of microRNA-22 and the luciferase reporter.
A: The possible transcription factors of microRNA-22 (miR-22) were predicted, of which Nr3c1 had the highest score; B: The luciferase reporter expression after the overexpression of Nr3c1; C: The predicted glucocorticoid receptor binding sites within the miR-22 promoter and the mutant versions generated by site mutagenesis are shown; D: The luciferase reporter expression after mutagenesis. MiR-22 promoter NC, mut 1, or mut 2 plasmid was co-transfected with Nr3c1 NC or Nr3c1 OE plasmid into AR42J cells, respectively. Dual luciferase reporter assays were performed 48 h after transfection; E: Results of the chromatin immunoprecipitation (ChIP) assay and ChIP-qPCR. Data were obtained from three independent experiments performed in triplicate and are shown as the mean ± SD. NSP > 0.05, aP < 0.05, bP < 0.01, cP < 0.001 vs Nr3c1 NC + miR-22 promoter NC, Nr3c1 NC + miR-22 promoter, Nr3c1 NC + miR-22 promoter WT, Nr3c1 OE + miR-22 promoter NC, Nr3c1 OE + miR-22 promoter WT or IgG groups. ChIP: Chromatin immunoprecipitation; GR: Glucocorticoid receptor; mut: Mutagenesis; OE: Overexpression; miR-22: MicroRNA-22.
- Citation: Fu Q, Liu CJ, Zhang X, Zhai ZS, Wang YZ, Hu MX, Xu XL, Zhang HW, Qin T. Glucocorticoid receptor regulates expression of microRNA-22 and downstream signaling pathway in apoptosis of pancreatic acinar cells. World J Gastroenterol 2018; 24(45): 5120-5130
- URL: https://www.wjgnet.com/1007-9327/full/v24/i45/5120.htm
- DOI: https://dx.doi.org/10.3748/wjg.v24.i45.5120