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. Author manuscript; available in PMC: 2020 Apr 18.
Published in final edited form as: Cell. 2019 Mar 28;177(3):654–668.e15. doi: 10.1016/j.cell.2019.02.010

Figure 6. Dentate Hopx+ neural progenitors maintain a stable landscape of chromatin accessibility across development.

Figure 6.

(A) PCA plot of ATAC-seq biological replicates of embryonic (E), early postnatal (P), and adult (A) dentate neural progenitors and adult dentate gyrus samples (N). ATAC-seq data for adult dentate gyrus is from (Su et al., 2017).

(B) Venn diagram illustrating the overlap of ATAC-seq peaks in dentate progenitors at different stages.

(C) Genome annotation of the dentate progenitor-enriched peaks, which were determined by comparing common peaks found in neural progenitors (B) to those in the adult dentate gyrus samples. TSS: transcription start site, TTS: transcription termination site.

(D) GO analysis of genes associated with progenitor enriched ATAC-seq peaks in the promoter-TSS, exon, intron, and TTS regions.

(E) Motif discovery analysis of dentate neural progenitor-enriched peaks or adult dentate gyrus-enriched peaks. Motifs shown are known transcription factor binding sites whose transcription factors were expressed in our samples and had an enrichment p-value ≤ 1×10−100.

(F-G) Representative chromatin profiling coverage of dentate neural progenitor-enriched peak with a Zfp354c binding site motif (F), and an adult dentate gyrus-enriched peak with a Neurod1/Tal1:Tcf3/Bhlha15 binding site motif (G). Y-axis indicates normalized reads. Black bars indicate peak locations.

See also Figure S4 & S6.