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SRX5026246: GSM3478692: Chip IgG Tet2+/+KitD816V; Mus musculus; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 45.2M spots, 3.4G bases, 1.4Gb downloads

Submitted by: NCBI (GEO)
Study: Tet2 is required for Socs activation in immune response cells [ChIP-seq]
show Abstracthide Abstract
Purpose: We have previously established an in vitro murine model that recapitulates the transformed phenotype of primary Tet2-/- mast cells expressing the Kit kinase domain mutant allele, D816V, that is both an oncogene and characterises patients with mastocytosis. To better understand the molecular basis of this cooperation and to further our understanding of role of Tet2 during inflammation and in other immune system disorders, we used this same in vitro primary cell system for genome wide studies to identify genes and genomic loci that are deregulated when these two mutations cooperate in mast cells. Overall design: ChIP-seq was performed on biological replicates with each ChIp antibody on 4 paired samples: 1) GFP-negative/control and 2) GFP-positive/KitD816V infected Tet2+/+ mast cells, and 3) GFP-negative/control and 4) GFP-positive/KitD816V infected Tet2-/- mast cells. Biological replicates constitute primary mast cell cultures derived from two individual mice of each genotype, cultured in parallel.
Sample: Chip IgG Tet2+/+KitD816V
SAMN10441262 • SRS4057700 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 4000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: The nuclei/chromatin suspension was sonicated using a Bioruptor Pico Sonnicator (Diagenode) for 20 cycles at 4°C. Sheared chromatin size was confirmed to be between 100-800 base-pairs on average by agarose gel. Two million cell equivalents were used for each ChIP. The following antibodies were used: H3K4me1 (Abcam, ab8895), H3K27ac (Abcam, ab4729), PU.1 (Santa Cruz Biotechnology, sc-352), Erg-1/2/3 (Santa Cruz Biotechnology, sc-354) and antibodies against total Stat5 (Santa Cruz, sc-835). ChIP samples were quantified using the Qubit Fluorometric quantification System (ThermoFisher) and using a DNA high sensitivity DNA kit on a Bioanalyzer (Agilent). ChIP-seq libraries were made using the Multiplex Library Preparation Kit (Diagenode). Nine cycles of PCR were used for all libraries. After library DNA was purified, library concentration was measured by Qubit, and size distribution was determined by Bioanalyzer. Each ChIP-seq library was sequenced for single-end reads of Illumina HiSeq 4000 (between 100-800 bp read length). Biological replicates for ChIP-seq were performed on independently derived primary mast cell cultures from 2 different mice for each sample and both sequenced.
Experiment attributes:
GEO Accession: GSM3478692
Links:
Runs: 1 run, 45.2M spots, 3.4G bases, 1.4Gb
Run# of Spots# of BasesSizePublished
SRR820692145,230,0433.4G1.4Gb2021-01-01

ID:
6779718

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