Chromatin modification of 15-LOX-1 promoter during transcriptional
activation. A, kinetics of depsipeptide effects on
dimethyl-histone H3 lysine 4 (H3K4me2) in the 15-LOX-1 promoter.
Caco-2 cells were treated with depsipeptide as indicated. ChIP/real-time PCR
was performed with the use of specific H3K4me2 or acetylated histone H3
(acetylated H3) antibodies. The results are the means ± S.D. of four
replicate experiments. B, effects of depsipeptide on H3 and H4
methylation patterns in the 15-LOX-1 promoter. Caco-2 cells were
treated with depsipeptide (5 nm) or solvent control, harvested 30
min later, and processed for ChIP/real-time PCR using anti-H3K9me1,
anti-H3K9me2, anti-H3K9me3, anti-H4K20me3, anti-H3K27me2, and anti-H3K27me3
antibodies. The results are the means ± S.D. of triplicate experiments.
C and D, kinetics of depsipeptide effects on H3 acetylation
and methylation. Caco-2 cells were treated with depsipeptide for the indicated
times and processed for ChIP/real-time PCR using antibodies against H3K9me2
(C) and H3K9ac (D). The results are the means ± S.D.
of four replicate experiments.