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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Nat Med. 2020 Jul 13;26(9):1452–1458. doi: 10.1038/s41591-020-0964-7

Extended Data Fig. 9. RNA-seq and ATAC-seq analyses of mMDSCs in tumor and bone marrow of mice exposed to MI or sham surgery.

Extended Data Fig. 9

(a) Heat map showing differential gene expression (log2FC) of select immune-related genes from RNA-Seq of tumoral CD11b+Ly6Chigh mMDSCs from mice 17 days post-MI (n=5) or sham (n=6) surgery (Padj<0.1). (b) Gene set concordance analysis showing that the top 1000 differentially expressed genes up- and down-regulated in tumor CD11b+Ly6Chigh mMDSCs (x axis) are enriched in genes up- and down-regulated in bone marrow Ly6Chigh monocytes (y axis) from the same mice 17 days post-MI, compared to background gene expression. (c) Gene ontology (GO) analyses of more accessible chromatin regions (n=942) in bone marrow Ly6Chigh monocytes from mice exposed to MI vs. sham surgery. (d) List of genes differentially expressed in tumor Ly6Chigh monocytes whose chromatin loci that are also less accessible in bone marrow Ly6Chigh monocytes after MI compared to sham surgery, grouped by transcription factors identified in Figure 3e. (e) ATAC-Seq (top) and RNA-Seq (bottom) reads in bone marrow and tumor Ly6Chigh monocytes at selected gene loci. P(adj) values were calculated using the Benjamini-Hochberg method (a). P values determined by two-sided Student’s T-test (b) or hypergeometric distribution (c).