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Status |
Public on Nov 24, 2010 |
Title |
Bcl6 and NFkB cistromes mediate opposing reulation of the innate immune response |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Here, using ChIP-seq, we define the NF-κB cistrome which is comprised of 31,070 cis-acting binding sites responsive to LPS-induced signaling. In addition, we demonstrate that the transcriptional repressor B-cell lymphoma 6 (Bcl-6) regulates nearly a third of the Tlr4-regulated transcriptome and that 90% of the Bcl-6 cistrome is collapsed following Tlr4 activation. Bcl-6 deficient macrophages are acutely hypersensitive to lipopolysaccharide (LPS) and, using comparative ChIP-seq analyses, we find that the Bcl-6 and NF-κB cistromes intersect, within nucleosomal distance, at nearly half of Bcl-6 binding sites in stimulated macrophages to promote opposing epigenetic modifications of the local chromatin. These results reveal a genomic strategy for controlling the innate immune response in which repressive and inductive cistromes establish a dynamic balance between macrophage quiescence and activation via epigenetically marked cis-regulatory elements.
keywords: Genome-wide location analysis
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Overall design |
Identification of BCL6 and NFkB binding sites in unstimulated and LPS-stimulated primary bone-marrow derived macrophages.
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Contributor(s) |
Yu RT, Barish GD, Evans RM |
Citation(s) |
21106671 |
Submission date |
Jun 19, 2009 |
Last update date |
May 15, 2019 |
Contact name |
Ruth T Yu |
Organization name |
Salk Institute
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Department |
Gene Expression Lab
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Lab |
Ronald Evans
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Street address |
10010 N Torrey Pines Rd
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City |
La Jolla |
State/province |
CA |
ZIP/Postal code |
92037 |
Country |
USA |
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Platforms (2) |
GPL9250 |
Illumina Genome Analyzer II (Mus musculus) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
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Samples (10)
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Relations |
SRA |
SRP001843 |
BioProject |
PRJNA117485 |