Mus musculus
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA173380 | ENA |
REPOSITORIES: ENA
Similar Datasets
Project description:This SuperSeries is composed of the following subset Series: GSE40238: Genome-wide maps of FoxP3 binding in transduced CD4+ T cells GSE40273: Gene expression profiling in Treg cells deficient or mutant in candidate FoxP3 cofactors GSE40274: Gene profiling data of CD4+ T cells transduced with FOXP3 and candidate cofactors GSE40276: Gene profiling data of CD4+ T cells transduced with FOXP3 and GATA1, then sorted into different fractions, based on the expression of Thy1.1 (FOXP3) GSE40277: Gene profiling data of CD4+ T cells doubly transduced with EOS+LEF1 or GATA1+SATB1 Refer to individual Series
2012-08-23 | E-GEOD-40278 | biostudies-arrayexpress
Project description:Expression data from mutant FoxP3-transduced CD4 T cells
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Project description:Transcription profiling by array of FOXP3 overexpression in resting and activated mouse CD4+ T cells
2016-03-08 | E-MTAB-4561 | ExpressionAtlas
Project description:Gene expression profiling in Treg cells deficient or mutant in candidate FoxP3 cofactors
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Project description:The transcription factor FoxP3 partakes dominantly in the specification and function of FoxP3+ CD4+ T regulatory cells (Tregs), but is neither strictly necessary nor sufficient to determine the characteristic Treg transcriptional signature. Computational network inference and experimental testing assessed the contribution of several other transcription factors (TFs). Enforced expression of Helios or Xbp1 elicited specific signatures, but Eos, Irf4, Satb1, Lef1 and Gata1 elicited exactly the same outcome, synergizing with FoxP3 to activate most of the Treg signature, including key TFs, and enhancing FoxP3 occupancy at its genomic targets. Conversely, the Treg signature was robust to inactivation of any single cofactor. A redundant genetic switch thus locks-in the Treg phenotype, a model which accounts for several aspects of Treg physiology, differentiation and stability. To study the impact of FoxP3 and its candidate cofactors (Eos, Gata1, Helios, Irf4, Lef1, Satb1, Xbp1) on the expression of the Treg transcriptional signature, CD4+ conventional T cells (Tconv) activated with anti-CD3+CD28 beads were retrovirally transduced with cDNAs encoding FOXP3, candidate TFs, or a combination of FOXP3 and candidate TFs. After 3 days in culture, the transduced cells were sorted into Trizol, and RNA was purified, labeled and hybridized to Affymetrix arrays.
2012-08-23 | E-GEOD-40274 | biostudies-arrayexpress
Project description:Expression data of Pioglitazone-, Rosiglitazone-, GW1929- and vehicle-treated CD4+FoxP3- T cells transduced with Foxp3+Pparg1
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Project description:Expression data of Pioglitazone- or vehicle-treated CD4+FoxP3- T cells transduced with Foxp3+/- Pparg1 (or Pparg2)
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Project description:Genome-wide maps of FoxP3 binding in transduced CD4+ T cells
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Project description:Gene profiling data of CD4+ T cells transduced with FOXP3 and GATA1, then sorted into different fractions, based on the expression of Thy1.1 (FOXP3)
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