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Status |
Public on Jun 14, 2017 |
Title |
Epigenetic analysis reveals the repressive function of MyoD during myogenic differentiation |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We identify a subset of highly expressed genes related to muscle development, which show static H3K4me2 enrichment over the gene body and H3K4me3 enrichment towards the gene body during myogenic differentiation. This study reveals that MyoD significantly binds to this particular subset of genes and further systematic analysis shows the repressive role of MyoD. Interestingly, MyoD binds and down-regulates Patz1 which is important for maintaining pluripotency. These findings might provide a key regulatory mechanism to promote myogenic differentiation.
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Overall design |
ChIP-seq profile of of two different histone modifications (H3K4me2 and H3K4me3) and a transcription factor MyoD during C2C12 cells differentiation.
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Contributor(s) |
Sperling SR |
Citation(s) |
28609469 |
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Submission date |
Nov 28, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Silke Sperling |
E-mail(s) |
silke.sperling@charite.de
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Phone |
++49 (0)30 450540123
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Organization name |
Experimental and Clinical Research Center (ECRC), Charité / MDC for Molecular Medicine
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Department |
Cardiovascular Genetics
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Lab |
Cardiovascular Genetics
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Street address |
Lindenberger Weg 80
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City |
Berlin |
State/province |
Berlin |
ZIP/Postal code |
13125 |
Country |
Germany |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (8)
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Relations |
BioProject |
PRJNA268849 |
SRA |
SRP050342 |