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Status |
Public on Nov 25, 2013 |
Title |
Genome-wide acetylated histone 3 lysine 9 (H3K9ac) in HDAC3-depleted liver rescued with deacectylase-dead HDAC3 mutants |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We found that several deacetylase-dead HDAC3 mutants were able to rescue the metabolic phenotype of HDAC3-depleted livers. Here we profile the histone acetylation in the presence of different HDAC3 mutants in mouse liver.
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Overall design |
Deacetylase-dead HDAC3 mutants, including HAHA, KA, YF and HEBI, were introduced into HDAC3-depleted (Cre) mouse livers by virus along with wild-type (WT) HDAC3 as a control. Livers were harvested at 5 pm (ZT 10) and subjected to ChIP with anti-H3K9ac antibodies followed by deep sequencing.
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Contributor(s) |
Fang B, Feng D, Sun Z, Lazar MA |
Citation(s) |
24268577 |
Submission date |
Jul 30, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Bin Fang |
E-mail(s) |
binfang@mail.med.upenn.edu
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Organization name |
University of Pennsylvania
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Lab |
Mitch Lazar
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Street address |
3400 Civic Center Blvd, Bldg 42
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City |
Philadelphia |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (1) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
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Samples (8)
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Relations |
BioProject |
PRJNA213727 |
SRA |
SRP028329 |