Transcriptomic data on the role of PEST-domain-enriched tyrosine phosphatase in the regulation of antigen-mediated activation and antiallergic action of glucocorticoids in mast cells

Data Brief. 2018 Sep 5:20:1177-1183. doi: 10.1016/j.dib.2018.08.188. eCollection 2018 Oct.

Abstract

Protein tyrosine phosphatases and glucocorticoids are known to regulate allergic and antiallergic action in activated mast cells. Here we provide RNA sequencing and quantitative real-time PCR data from bone marrow derived mast cells, for wild-type and PEST-domain-enriched tyrosine phosphatase (PEP) null mice, activated by immunoglobulin E sensitization and dinitrophenol treatment, and additionally treated with the glucocorticoid dexamethasone. The transcriptomics experiment was performed in duplicate with a total of 16 samples (GSE108972).

Keywords: Allergy; BMMCs, Bone marrow derived mast cells; COX-2, Cyclooxygenase 2; CSF2, Colony stimulating factor 2; DAVID, Database for Annotation, Visualization and Integrated Discovery; DEX, Dexamethasone; DNP, Dinitrophenol; Gene expression; IL 13, Interleukin 13; IMDM, Iscove׳s Modified Dulbecco׳s Medium; IgE, Immunoglobulin E; KEGG, Kyoto Encyclopedia of Genes and Genomes; PCA, Principal Component Analysis; PEP, PEST-domain-enriched tyrosine phosphatase; PTGDS, Prostaglandin D2 synthase - lipocalin type; Phosphatase; Quantitative real-time PCR; RNA sequencing; RNA-seq, RNA-sequencing; SBS, Sequencing by Synthesis; TNFα, Tumor necrosis factor alpha; qRT-PCR, Quantitative real-time polymerase chain reaction.