Fig. 1 | Nature Communications

Fig. 1

From: High-resolution visualization of H3 variants during replication reveals their controlled recycling

Fig. 1

Global H3.3 and H3.1 genome-wide occupancy relative to replication timing and transcriptional activity. a H3.3 and H3.1 genomic coverage normalized to input (chromosome 3 centromeric band±15 Mb, x-axis). The y-axis shows the log2 ratio between the mean per-base number of reads from H3.3 (green) and H3.1 (purple) and their respective input, at consecutive 10 kb bins (smoothed over 5 non-zero bins). Enriched regions (i.e., log2 ratio ≥ 0) are highlighted in darker colors. b H3.3 and H3.1 occupancy by replication timing: the panels show the histogram and Gaussian kernel density corresponding to the log2 ratio to input for H3.3 (green) and H3.1 (purple) at 10 kb regions ranked by replication timing from early to late (S-phase fraction with the highest mean coverage in Repli-Seq data from Dellino et al.38). c Mean values corresponding to b. d H3.3 and H3.1 occupancy by replication timing at increasing levels of nascent transcription: the mean log2 ratio to input for H3.3 (green, left) and H3.1 (purple, right) at 10 kb regions ranked by replication timing (as in b) and transcription percentile (based on nascent RNA-Seq data from Liang et al.53). The color gradient represents increasing levels of nascent transcription computed from the log2-transformed mean coverage: absence of measurable transcription (none), lower 10th percentile (low), 10th to 90th percentile (mid) or upper 10th percentile (high). e H3.3 and H3.1 correlation with early DNA synthesis at increasing transcription levels. H3.3 (top) and H3.1 (bottom) log2 ratio to input (x-axis) against S1 coverage normalized to the average over all fractions (log2 ratio, z-axis) at 10 kb regions ranked by transcriptional status (y-axis). The rank reflects the level of nascent transcription as described above

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