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Series GSE22104 Query DataSets for GSE22104
Status Public on Jun 18, 2010
Title Discrete Roles of STAT4 and STAT6 Transcription Factors in Tuning Epigenetic Modifications and Transcription during Helper T Cell Differentiation (ChIP-Seq)
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Signal transducer and activator of transcription 4 (STAT4) and STAT6 are key factors in the specification of helper T cells; however, their direct roles in driving differentiation are not well understood. Using chromatin immunoprecipitation and massive parallel sequencing, we quantitated the full complement of STAT-bound genes, concurrently assessing global STAT-dependent epigenetic modifications and gene transcription using cells from cognate STAT-deficient mice. STAT4 and STAT6 each bound over 4000 genes with distinct binding motifs. Both played critical roles in maintaining chromatin configuration and transcription of a core subset of genes through the combination of different epigenetic patterns. Globally, STAT4 had a more dominant role in promoting active epigenetic marks, whereas STAT6 had a more prominent role in antagonizing repressive marks. Clusters of genes negatively regulated by STATs were also identified, highlighting previously unappreciated repressive roles. Therefore, STAT4 and STAT6 play wide regulatory roles in T helper specification.
 
Overall design The roles of STAT proteins to shape T helper cell phenotype was investigated by comparing DNA binding profiles of STAT4 and STAT6 in Th1 and Th2 conditions. The functional outcome of STAT bindings was further evaluated by profiling histone epigenetic marks and gene expression changes between WT and STAT-deficient T cells in Th1 and Th2 conditions.
 
Contributor(s) Wei L, Vahedi G, Sun H, Watford WT, Takatori H, Ramos HL, Takahashi H, Liang J, Gutierrez-Cruz G, Zang C, Peng W, O’Shea JJ, Kanno Y
Citation(s) 20620946, 23555662
Submission date Jun 02, 2010
Last update date Feb 12, 2020
Contact name Golnaz Vahedi
Organization name National Institutes of Health
Department NIAMS
Lab Lymphocyte Cell Biology Section
Street address 9000 Rockville Pike Bldg 10 Rm 13C101A
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platforms (1)
GPL9185 Illumina Genome Analyzer (Mus musculus)
Samples (17)
GSM550303 Stat4WTTh1
GSM550304 Stat4KOTh1
GSM550305 H3K4me3WTTh1
This SubSeries is part of SuperSeries:
GSE22105 Discrete Roles of STAT4 and STAT6 Transcription Factors in Tuning Epigenetic Modifications and Transcription during Helper T Cell Differentiation
Relations
SRA SRP002570
BioProject PRJNA129179

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Supplementary file Size Download File type/resource
GSE22104_RAW.tar 1.1 Gb (http)(custom) TAR (of BED, BEDGRAPH, TXT)
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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