Skip to main content
. 2019 Mar 8;30(4):594–609. doi: 10.1681/ASN.2018070687

Figure 7.

Figure 7.

RIG-I-Like signaling and apoptosis are increased in kidneys of Six2Cre Dnmt1f/f mice. (A) The GSEA enrichment plots of RNA sequencing data showing enrichment for RIG-I–like signaling in Six2Cre Dnmt1f/f mice. (B) Relative expression level of genes involved in RIG-I–like signaling. y-axis is normalized expression level determined by RNA sequencing. Asterisks represent significant differences calculated by DESeq2. (C) The GSEA enrichment plots of RNA sequencing data of P53 signaling in Six2Cre Dnmt1f/f mice. (D) Relative expression level of genes involved in p53 signaling. y-axis is normalized expression level determined by RNA sequencing. Asterisks represent significant differences calculated by DESeq2. (E) Left panel: immunofluorescence staining of P53 (red) and TUNEL assay (red) in P0 Dnmt1f/f and Six2Cre Dnmt1f/f mice kidneys; right panel: quantification of P53- and TUNEL-positive signaling according to the staining. (F) Left panel: immunofluorescence staining of Ki67 (red) in P0 Dnmt1f/f and Six2Cre Dnmt1f/f mice kidneys; right panel: quantification of Ki67-positive cells. (G) Schematic of our model which Dnmt1 deletion in progeny of Six2-positive cells affects kidney development. *P<0.05 and ***P<0.001.