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. 2021 Jul 2;12:4105. doi: 10.1038/s41467-021-24352-w

Fig. 1. MCPIP3 is positively associated with psoriasis pathogenesis.

Fig. 1

a Schematics indicating the location of SNP rs4561177 in human ZC3H12C. b Regulation of ZC3H12C expression by SNP rs4561177 was measured by a luciferase reporter system. The promoter region (~1 kb) containing the SNP was inserted upstream of the luciferase gene, and then transfected into 293 T cells for assessment of reporter activity (R.L.U) (n = 6 replicates). c ZC3H12C expression in psoriatic lesion (red) and non-lesions biopsies (blue) from psoriasis patients were analyzed (n = 28 individuals in GDS3539; n = 85 individuals in GDS4600). d ZC3H12C expression in psoriatic lesions after brodalumab treatment (GEO: GSE53552) was analyzed (n = 5 individuals for placebo, 8 individuals for brodalumab). e ZC3H12C expression in human peripheral blood mononuclear cells (PBMC) immune populations was measured by qPCR (n = 6 individuals for PMBC; n = 11 individuals for other groups). f Zc3h12c expression in murine WT immune populations was measured by qPCR (n = 3 mice per group). g Zc3h12c expression in sorted Zc3h12c fl/fl (blue) /Zc3h12c DCΔ (red) BM plasmacytoid dendritic cells (pDCs) was measured by qPCR after stimulation (n = 3 mice per group). h Zc3h12c expression in R848-treated Zc3h12c+/+ (blue)/Zc3h12c−/−(red) bone marrow-derived macrophages (BMDMs) was measured by qPCR at indicated timepoints (n = 3 mice per group). Data are representative at least three independent experiments (mean ± S.D.; two-tailed Student’s t test for murine samples; two-tailed Wilcoxon matched-pair signed rank test for human samples). Source data are provided as a Source Data file.