MYS‐1 binding and histone H4K16 acetylation status were examined by ChIP–qPCR using crosslinked DNA–protein complexes isolated from the indicated RNAi‐treated N2 worms at day 2 adulthood with anti‐Tip60/MYS‐1, anti‐AcH4K16 and control IgG antibody. The bars represent the percentage of total input DNA for each ChIP sample, and error bars represent the SD derived from three independent experiments. **
P < 0.01, ***
P < 0.001, one‐way ANOVA followed by Tukey's test. See also Fig
EV3.