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Status |
Public on Sep 10, 2015 |
Title |
ChIP-seq assays for H3K27ac |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
By using FACS-sorted MC1-ZE7 ES cells, we analyzed the genome-wide distribution of H3K27ac and DNA methylation in Zscan4 positive ES cells (Em+) and Zscan4 negative ES cells (Em-). H3K27 hyperacetylation and DNA demethylation were detected in heterochromatic regions of Em+ cells, but not Em- cells. These results suggested that the Zscan4 state takes "open" chromatin conformation in ES cells.
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Overall design |
H3K27ac in Zscan4 positive and negative cells
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Contributor(s) |
Akiyama T |
Citation(s) |
26324425 |
Submission date |
Oct 24, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Minoru S.H. Ko |
E-mail(s) |
kom@mail.nih.gov
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Phone |
410-558-8359
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Organization name |
NIH
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Department |
National Institute on Aging
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Lab |
Lab of Genetics
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Street address |
251 Bayview Blvd, Suite 100, 10C
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City |
Baltimore |
State/province |
MD |
ZIP/Postal code |
21224 |
Country |
USA |
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Platforms (1) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
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Samples (4)
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GSM1250436 |
MC1-ZE7 cells (Em+ high fraction) H3K27ac rep2 |
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This SubSeries is part of SuperSeries: |
GSE51682 |
Zscan4 mediates transient remodeling and transcriptional burst of heterochromatin in mouse embryonic stem cells |
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Relations |
BioProject |
PRJNA224548 |
SRA |
SRP031895 |