a, Aggregated profiles visualize the increase of H3K9ac
at the most dynamic 200 genes after short low R:FR exposures (5, 10 and 30
min). H3K9ac occupancy was determined in WL and low R:FR-exposed
pif457 PIF7:PIF7:4xMYC seedlings by ChIP-seq and was
calculated as the ratio between WL and low R:FR-treated H3K9ac ChIP-seq
samples. b, AnnoJ genome browser screenshot visualizes PIF7
binding and H3K9 acetylation at the ATHB2 gene and its
closest relatives (ATHB4, HAT2,
HAT3). Genome-wide occupancy of PIF7 and H3K9ac under
constant light conditions was determined in the same pif457
PIF7:PIF7:4xMYC chromatin by ChIP-seq whereas under LD
conditions at ZT4, WT (H3K9ac), pif457 (H3K9ac) and
pif457 PIF7:PIF7:4xMYC (PIF7) chromatin was used. All
tracks were normalized to the respective sequencing depth. The areas marked
in red indicate PIF7 binding and H3K9 hyperacetylation. c,
Quantification of relative H3K9ac levels at the promoters of
ATHB2, ATHB4, HAT2
and HAT3 in low R:FR-exposed pif457
PIF7:PIF7:4xMYC seedlings. H3K9ac occupancy was calculated as
the ratio between the respective ChIP-seq sample from one experiment and the
WT IgG control. d, Aggregated profiles visualize the increase
of H3K9ac at the most dynamic 200 genes after 4 hours of low R:FR exposure
at ZT4. H3K9ac occupancy was determined in WL and low R:FR-exposed WT and
pif457 seedlings by ChIP-seq and was calculated as the
ratio between WL and low R:FR-treated H3K9ac ChIP-seq samples.
e, Quantification of relative H3K9ac levels at the
promoters of ATHB2, ATHB4,
HAT2 and HAT3 in WL and low
R:FR-exposed WT and pif457 seedlings. H3K9ac occupancy was
calculated from one experiment as the ratio between the H2A.Z ChIP-seq
sample and the WT IgG control.