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. 2023 Feb 13;2(2):174–191. doi: 10.1038/s44161-023-00214-0

Extended Data Fig. 1. Kdm8 demethylates H3K36me2 in the heart.

Extended Data Fig. 1

a, Percentage of genotypes of male offspring from control Kdm8fl/fl females crossed with mutant Kdm8fl/fl;Myh6-Cre males. Data was analyzed by two-tailed chi-squared test. b, qPCR of Kdm8 normalized to Rpl13a in whole ventricles of 2-month-old control, heterozygous (Kdm8fl+;Myh6-Cre), and mutant mice. Error bars denote the mean + /- s.d. Data was analyzed by one-way ANOVA with Tuckey’s multiple comparison correction. n = 5 hearts per group. c, qPCR of Kdm8 in isolated cardiomyocytes (CMs) and in the non-cardiomyocyte cell fraction (non CMs) of 2-month-old control and mutant hearts. Error bars denote the mean + /- s.d. Data was analyzed by two-way ANOVA. n = 3 control and 5 mutant hearts. qPCR in b and c were repeated twice with similar results. d, Western blot of Kdm8 in whole ventricles at 6 months of age. e, Band intensity of Kdm8 protein normalized to histone H3 (H3) (shown in d) and analyzed by unpaired two-tailed Student’s t-test. n = 5 hearts per group. Error bars denote the mean + /- s.e.m. f, Histone demethylase (HDM) activity of Jumonji domain-containing proteins, shown as fluorescence units, on extracts of control and mutant hearts at 5 weeks of age. Error bars denote the mean + /- s.d. Data was analyzed by unpaired two-tailed Student’s t-test. n = 5 control and 4 mutant hearts. g, Western blot of H3K36me2 in whole ventricles at 2 months of age. h, Band intensity of H3K36me2 normalized to H3 (shown in g) and analyzed by two-tailed Student’s t-test. error bars denote the mean + /- s.e.m. n = 5 control and 5 mutant hearts.

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