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Status |
Public on Feb 11, 2011 |
Title |
IGH analysis in pro-B cells with H3K4me3, H3K4me2, H3K9ac, H3K27me3, Pax5 and CTCF [ChIP-Seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
VH-DJH recombination of the immunoglobulin heavy-chain (Igh) locus is temporally and spatially controlled during early B-cell development, and yet no regulatory elements other than the VH gene promoters have been identified throughout the entire 2.5-Mb VH gene cluster. Here we discovered novel regulatory sequences that are interspersed in the distal VH gene region. These conserved repeat elements were characterized by the presence of Pax5-dependent active chromatin, the binding of Pax5, E2A, CTCF and Rad21 as well as by Pax5-dependent antisense transcription in pro-B cells. The Pax5-activated intergenic repeat (PAIR) elements were no longer bound by Pax5 in pre-B and B cells consistent with the loss of antisense transcription, whereas E2A and CTCF interacted with PAIR elements throughout early B-cell development. The pro-B-cell-specific and Pax5-dependent activity of the PAIR elements suggests that they are involved in the regulation of distal VH-DJH recombination at the Igh locus.
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Overall design |
Analysis of chromatin and TF binding in rag2-/- and wt pro-B, DP T and Mature B cells. Chip-Seq of CTCF and Rad21. The provided data is in mm8 coordinates.
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Contributor(s) |
Ebert A, McManus S, Busslinger M, Novatchkova M, Jaritz M |
Citation(s) |
21349430, 21552207 |
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Submission date |
Feb 10, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Meinrad Busslinger |
E-mail(s) |
busslinger@imp.ac.at
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Phone |
00431-79730
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Organization name |
Instutute of Molecular Pathology
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Street address |
Dr. Bohrgasse 7
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City |
Vienna |
ZIP/Postal code |
1030 |
Country |
Austria |
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Platforms (1) |
GPL9185 |
Illumina Genome Analyzer (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE27215 |
IGH analysis in pro-B cells with H3K4me3, H3K4me2, H3K9ac, H3K27me3, Pax5 and CTCF |
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Relations |
SRA |
SRP005684 |
BioProject |
PRJNA141973 |