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Sample GSM5224986 Query DataSets for GSM5224986
Status Public on Mar 30, 2022
Title EL4 GFP + GATA3 HA-GATA3 ChIP rep1
Sample type SRA
 
Source name EL4 cell line
Organism Mus musculus
Characteristics treatment: PMA + inomomycin
ectopically expressed protein: HA-GATA3
cell line: EL4
antibody: anti-HA, 3F10 Roche
Treatment protocol EL4 cells were stimulated with phorbol 12-myristate 13-acetate (50 ng/ml) and ionomycin (1 μM) for 4 hours prior to crosslinking. Cells were crosslinked by the addition of one-tenth volume of fresh 11% formaldehyde solution for 20 minutes at room temperature before the reaction was quenched by addition of glycine as described. Cells were rinsed twice with 1xPBS and flash frozen in liquid nitrogen.
Growth protocol EL4 cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum, 4 mM L-alanyl-L-glutamine, 25 mM D-glucose, 1 mM sodium pyruvate, 10 mM HEPES, 100 U/ml penicillin and 100 µg/ml streptomycin
Extracted molecule genomic DNA
Extraction protocol Cells were lysed with non-ionic detergent, the nuclei washed and then lysed with ionic detergent. Cells were sonicated on ice to solubilize and shear crosslinked DNA (27W for 10x 30 second pulses using a Misonix Sonicator 3000). The resulting whole cell lysate was cleared by centrifugation and then incubated overnight at 4°C with 50 µl of Protein G magnetic Dynabeads that had been pre-incubated with 5 µg of purified antibody (anti-FLAG, M2 Sigma; anti-HA, 3F10 Roche; anti-H3K27ac, ab4729 Abcam). Beads were washed 6 times with RIPA buffer and 1 time with TE containing 50 mM NaCl. Bound complexes were eluted from the beads by heating at 65°C with rocking for 2 hrs and crosslinks then reversed in IP and input DNA by incubation at 65°C for 6 hrs. IP and input DNA were then purified by treatment with RNase A, proteinase K and isolated with KAPA Pure beads.
Libraries were constructed from ChIP DNA by standard Illumina protocols, except that DNA in the range 150-350 bp was gel-purified after PCR-amplification. The libraries were quantified using a Qubit and Agilent bioanalyzer, pooled and subjected to 50 bp single-end read sequencing with a HiSeq 2500 sequencer.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2500
 
Data processing Raw reads were filtered for base quality using FastQC with default parameters and adapters sequences were removed with Trim Galore!
Reads passing quality filtering criteria were aligned to GRCm38 using BWA with default settings
Genome_build: mm10
Supplementary_files_format_and_content: bigwig
 
Submission date Apr 02, 2021
Last update date Mar 30, 2022
Contact name Arnulf Hertweck
E-mail(s) a.hertweck@ucl.ac.uk
Organization name University College London
Department UCL Cancer Institute
Street address Gower Street
City London
ZIP/Postal code WC1E 6BT
Country United Kingdom
 
Platform ID GPL17021
Series (2)
GSE171408 The TH1 cell lineage-determining transcription factor T-bet supresses TH2 gene expression by redistributing GATA3 away from TH2 genes [ChIP-seq]
GSE171410 The TH1 cell lineage-determining transcription factor T-bet supresses TH2 gene expression by redistributing GATA3 away from TH2 genes
Relations
BioSample SAMN18605342
SRA SRX10505875

Supplementary file Size Download File type/resource
GSM5224986_EL4_GFP_GATA3_HA-GATA3_rep1.bw 123.8 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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