The SWI/SNF subunit Dpf2 licenses Nrf2-dependent gene expression to enforce multilineage control of inflammation [RNA-seq]

ABSTRACT: Purpose: Multi-omics characterization of the consequences of deleting the SWI/SNF subunit Dpf2 in the transcriptome (RNAseq), accessibility of the genome (ATACseq) and binding of SWI/SNF subunits (CUT&RUN) in hematopoietic stem/progenitor cells, resting and polarized bone-marrow derived macrophages and resting and activated CD4+ T cells obtained from Dpf2f/f and Dpf2D/D mice. Methods: Lin- cKit+ cells were sorted from bone marrow of 28-days old Dpf2f/f and Dpf2D/D mice. Bone-marrow derived macrophages were obtained from 28-days old Dpf2f/f and Dpf2D/D mice and polarized with IFNg and LPS, or IL-4 for 24hours. CD4+ splenic T helper cells were obtained from 28-days old Dpf2f/f and Dpf2D/D mice and activated by treatment with PMA and Ionomycin. Methods: For RNAseq, total RNA was extracted using RNEasy Plus micro kit (Qiagen). Ribosomal RNA was removed using NEBNext rRNA Depletion kit and RNAseq libraries were prepared using Illumina's TruSeq total stranded RNAseq prep kit (NuGEN Technologies). RNAseq libraries were sequenced on an Illumina NextSeq500 prep kit (Paired-end, 75bp) or NovaSeq 6000. Results: For RNAseq samples, we obtained more than 40 million paired-end reads per sample. Reads were aligned to the mm10 transcriptome and ERCC spike-in indexes using RSEM (v1.3.0) and STAR (v2.6.0c) with Gencode annotations. Differentially expressed genes were determined by DESeq2 (v1.18.1, Wald Test, p-adj<0.05) after gene counts were corrected based on ERCC variances using RUVseq (v1.12.0). Conclusions: The absence of Dpf2 in LK cells results in downregulation of anti-oxidative and anti-inflammatory gene expression programs in bone marrow LK cells, bone-marrow derived macrophages and CD4+ T cells.

ORGANISM(S): Mus musculus Homo sapiens

PROVIDER: GSE192775 | GEO | 2023/06/06

REPOSITORIES: GEO