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Comment
. 2022 Jun 29;13(1):3725.
doi: 10.1038/s41467-022-30351-2.

Reply to: Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription

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Comment

Reply to: Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription

Benjamin J E Martin et al. Nat Commun. .
No abstract available

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Transcription inhibition by 1,10-phenanthroline (1,10-pt) does not impact Epl1 occupancy at most promoters.
Scatter plots comparing the effect of 1,10-pt on fragment midpoint counts from Epl1 (a, d), H4K8ac (b, e), or H4K12ac (c, f) ChIP-seq, over promoters (a and d) or associated +1 nucleosomes (b, c, e, and f) of all (5542) genes (a, b, c) or of 562 genes with NDR Epl1 peaks identified in MNase ChIP-seq in control cells (d, e, f). Promoters with >1.5 fold-change in Epl1 using an adjusted p-value < 0.1 (DESeq2’s binomial test) are shown in red (increased) or blue (decreased). In b, c, e, and f, the line is: y = x + 0.
Fig. 2
Fig. 2. Transcription inhibition with 1,10-phenanthroline (1,10-pt) does not mirror the effect of heat shock on RNAPII occupancy at most genes.
a Scatter plot comparing the log2 fold change (FC) in RNAPII occupancy following treatment with 1,10-pt with RNAPII serine 5 phosphorylation (s5p) following heat shock in gene 5′ regions (TSS to +400 bp) for all (5542) genes. b PCA plot showing the first two principal components calculated across TSS to +400 bp for all (5542) genes. c NET-seq 3′ read counts from TSS to +400 nt (sense), TSS to −400 nt (antisense), or in NDRs (antisense) depicted by violin plots for all (5542) genes.

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