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Series GSE115433 Query DataSets for GSE115433
Status Public on May 28, 2019
Title STAT1, STAT2 and IRF9 transcription factor binding analysis in wild type and Irf9-/- bone marrow derived macrophages in response to type I and type II interferons
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Host defense by the innate immune system requires the establishment of antimicrobial states allowing cells to cope with microorganisms before the onset of the adaptive immune response. Interferons (IFN) are of vital importance in the establishment of cell-autonomous antimicrobial immunity. Speed is therefore an important attribute of the cellular response to IFN. With much of the antimicrobial response being installed de novo, this pertains foremost to gene expression, the rapid switch between resting-state and active-state transcription of host defense genes. Mechanisms to meet this demand on the relevant molecular machinery include remodeling of chromatin but also changes in transcription factor interaction prior and during the IFN response. Our results show how transcription factors STAT1, STAT2 and IRF9 change binding patterns upon IFNb or IFNg treatment in wild type and Irf9-/- bone marrow derived macrophages.
 
Overall design Methods: Genome wide binding of transcription factors STAT1, STAT2 and IRF9 in untreated, 90 min IFNb and 90 min IFNg treated wild-type (WT) and Irf9 knock out (IRF9-/-) bone marrow derived macrophages. Biological duplicates were analyzed by using Illumina sequencing.
 
Contributor(s) Platanitis E, Decker T
Citation(s) 31266943, 35243225
https://doi.org/10.1101/377275
Submission date Jun 06, 2018
Last update date Mar 09, 2022
Contact name Ekaterini Platanitis
Organization name University of Vienna
Department Department of Microbiology, Immunobiology and Genetics
Street address Dr.-Bohr-Gasse 9
City Vienna
ZIP/Postal code 1030
Country Austria
 
Platforms (1)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
Samples (31)
GSM3178193 input
GSM3178194 WT STAT1 rep1
GSM3178195 WT STAT1 rep2
This SubSeries is part of SuperSeries:
GSE115435 Irf9 function in immunity in mouse
Relations
BioProject PRJNA474952
SRA SRP149943

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE115433_K_STAT1_b_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 151.4 Kb (ftp)(http) NARROWPEAK
GSE115433_K_STAT1_g_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 163.3 Kb (ftp)(http) NARROWPEAK
GSE115433_K_STAT1_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 2.2 Kb (ftp)(http) NARROWPEAK
GSE115433_K_STAT2_b_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 274.8 Kb (ftp)(http) NARROWPEAK
GSE115433_K_STAT2_g_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 6.1 Kb (ftp)(http) NARROWPEAK
GSE115433_K_STAT2_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 2.5 Kb (ftp)(http) NARROWPEAK
GSE115433_RAW.tar 39.4 Mb (http)(custom) TAR (of NARROWPEAK)
GSE115433_W_IRF9_b_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 317.9 Kb (ftp)(http) NARROWPEAK
GSE115433_W_IRF9_g_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 98.4 Kb (ftp)(http) NARROWPEAK
GSE115433_W_IRF9_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 13.0 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT1_b_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 159.5 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT1_g_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 171.0 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT1_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 1.8 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT2_b_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 376.6 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT2_g_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 86.7 Kb (ftp)(http) NARROWPEAK
GSE115433_W_STAT2_ppr.peak.spp.idr.optimal_set.IDR0.01.filt.narrowPeak.gz 14.8 Kb (ftp)(http) NARROWPEAK
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Raw data are available in SRA
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