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Status |
Public on Mar 01, 2016 |
Title |
Distinct activities of Myf5 and MyoD indicate sequential roles in skeletal muscle lineage specification and differentiation (ChIP-Seq) |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
In this work we compare the molecular functions of Myf5 and MyoD, two highly related bHLH transcription factors that regulate skeletal muscle specification and differentiation. We find MyoD and Myf5 bind the same sites genome-wide but have distinct functions: Myf5 induces histone acetylation without Pol II recruitment or robust gene activation, whereas MyoD induces histone acetylation, recruits PolII and robustly activates gene transcription.
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Overall design |
Chip-seq profiling of MyoD, Myf5, Histone H4 acetylation (H4Ac), and Pol II in MyoD-/-; Myf5-/- MEFs (M&M MEFs)
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Contributor(s) |
Conerly ML, Yao Z, Zhong JW, Groudine M, Tapscott SJ |
Citation(s) |
26906734 |
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Submission date |
Nov 24, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Stephen Tapscott |
E-mail(s) |
stapscot@fredhutch.org
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Organization name |
Fred Hutch Cancer Research Center
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Department |
Human Biology
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Lab |
Tapscott
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Street address |
1100 Fairview N. Ave
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City |
Seattle |
State/province |
WASHINGTON |
ZIP/Postal code |
98103 |
Country |
USA |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (10)
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This SubSeries is part of SuperSeries: |
GSE75632 |
Distinct activities of Myf5 and MyoD indicate sequential roles in skeletal muscle lineage specification and differentiation |
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Relations |
BioProject |
PRJNA304013 |
SRA |
SRP066628 |