Fig. 4 | Nature Communications

Fig. 4

From: Pax3 cooperates with Ldb1 to direct local chromosome architecture during myogenic lineage specification

Fig. 4The alternative text for this image may have been generated using AI.

Ldb1 recruitment at Pax3 sites is associated with enhanced chromatin remodeling and looping. a k-means clustering of ChIP-seq data for LDB1, SMC1, and CTCF in 1-day Pax3-induced (+) and non-induced (−) EBs. Density Tag Map centered on 3780 PAX3 peaks shows the recruitment of LDB1 upon Pax3 induction at a subset of loci (cluster 1), and reveals that PAX3-mediated LDB1 recruitment is independent from SMC1-CTCF complex. Cluster 1: 595 peaks; Cluster 2: 168 peaks; Cluster 3: 324 peaks; Cluster 4: 2693 peaks. b IGV track displaying PAX3, LDB1, SMC1, and CTCF genome occupancy at the Megf10 locus in 1-day Pax3-induced (+) and non-induced (−) EBs. Dashed black square indicate PAX3-mediated LDB1 recruitment. Green boxes represent intergenic regions. Black arrow represents the transcription start site. c Graph shows distribution of ChIP-seq reads for the selected marks at loci characterized by PAX3 + LDB1 recruitment (violet) and PAX3-only binding (green). Loci bound by both LDB1 and PAX3 display higher remodeling compared with PAX3-only bound sites. d HiChIP normalized matrix from 6-day Pax3-induced cells displaying the Megf10 locus demonstrates long-range interactions involving the 1-day bound PAX3 + LDB1 site (dashed black square from panel b). Position of PAX3 peaks, genes and chromosome coordinates are showed below the matrix. Scale: maxrange = 0.2. Arcs indicate looping interactions identified by FitHiChIP. e GREAT functional annotation of peaks characterized by PAX3-mediated LDB1 recruitment (cluster from Fig. 4a)

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