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Status |
Public on May 15, 2013 |
Title |
Mechanisms of PU.1 binding site selection in-vivo |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Methylation profiling by high throughput sequencing
|
Summary |
The majority of sequence-specific transcription factors bind genomic DNA only at a fraction of their potential binding sites and the ‘rules’ for binding or not-binding are only partially understood. Here, we studied the binding properties of the myeloid and B-cell specific transcription factor PU.1 in-vivo and in-vitro to unveil basic features of occupied vs. non-occupied consensus sites. In addition to published PU.1 ChIP-seq data we mapped CTCF binding sites in monocytes and macrophages to determine chromatin domain boundaries and performed MCIp-seq in monocytes to reveal DNA methylation patterns across the genome.
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Overall design |
ChIP-seq of CTCF in human monocytes and human monocyte-derived macrophages as well as MCIp-seq in human monocytes
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Contributor(s) |
Rehli M |
Citation(s) |
23658224 |
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Submission date |
Dec 21, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Michael Rehli |
E-mail(s) |
michael.rehli@klinik.uni-r.de
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Organization name |
University Hospital Regensburg
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Department |
Internal Med III
|
Street address |
F.-J.-Strauss-Allee 11
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City |
Regensburg |
ZIP/Postal code |
93042 |
Country |
Germany |
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Platforms (1) |
GPL9052 |
Illumina Genome Analyzer (Homo sapiens) |
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Samples (3) |
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Relations |
SRA |
SRP017647 |
BioProject |
PRJNA185267 |