Fig. 1: JMJD3 epigenetically activates hepatic autophagy-network genes.

JMJD3-floxed mice were infected with AAV-TBG-Cre or control AAV-GFP for 12 weeks, and then, fasted for 16āh. a Experimental outline (top) and the levels of JMJD3 detected by IB in the liver and intestine (bottom). b RNA-seq: heat maps of changes in mRNA levels of autophagy-related genes (nā=ā3 mice). c ChIP-seq: normalized H3K27-me3 peaks at hepatic genes involved in autophagic pathways (UCSC genome browser). d Venn diagram (top) of downregulated genes and genes with increased H3K27-me3 levels after liver-specific downregulation of JMJD3 and G/O analysis (bottom) of the hepatic genes that show both increased H3K27-me3 levels and decreased expression.āe The mRNA levels of the indicated genes in liver of mice fasted for 16āh (Fs) or refed (Fd) for 6āh after fasted for 10āh were measured by q-RTPCR (nā=ā5ā10 mice). f, g ChIP assays: effects of the downregulation of JMJD3 on f H3K27-me3 levels and g occupancy of JMJD3 at the indicated genes (nā=ā3 mice). Source data are provided as a Source Data file. All values are presented as meanā±āSD. Statistical significance was measured using the eāg two-way ANOVA with the Bonferroni post-test. *Pā<ā0.05, **Pā<ā0.01, and NS statistically not significant.