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Status |
Public on Aug 07, 2019 |
Title |
Mapping Bcl11b binding in regulatory T cells |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
T regulatory (Treg) cells have been studied in depth since their discovery for their potential use in therapies of autoimmune diseases. Treg cells have a suppression program that includes surface molecules CD25 (IL2R), cytotoxic T-lymphocyte associated protein 4 (CTLA4), and glucocorticoid-induced TNFR family (GITR) to limit aberrant and excessive inflammatory immune responses. We have shown that Bcl11b can bind to the CNS2 region in Foxp3 as well as the gene loci of those essential surface molecules for Treg suppression. Furthermore, we have identified a subset of Foxp3-independent genes in Treg cells directly regulated by Bcl11b binding. Bcl11b also directly represses expression of innate molecules such as transcription factors PU.1 and ID2 in Treg cells. Finally, we have also shown that removal of Bcl11b accelerates apoptosis in Treg cells as cleaved caspase 3 levels were significantly elevated in Bcl11b KO Treg cells when compared with WT Treg cells.
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Overall design |
Examination of Bcl11b binding in regulatory T cells from steady state mice
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Contributor(s) |
Drashansky T, Helm E, Huo Z, Avram D |
Citation(s) |
31457080 |
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Submission date |
Oct 05, 2018 |
Last update date |
Nov 06, 2019 |
Contact name |
Dorina Avram |
E-mail(s) |
[email protected]
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Organization name |
Moffitt Cancer Center
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Department |
Department of Immunology
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Lab |
Avram lab
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Street address |
12902 Magnolia Drive, MRC4
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City |
Tampa |
State/province |
Fl |
ZIP/Postal code |
33612 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (3) |
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This SubSeries is part of SuperSeries: |
GSE120875 |
Genome wide mapping in regulatory T cells at steady state |
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Relations |
BioProject |
PRJNA494809 |
SRA |
SRP163620 |