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Status |
Public on Jun 07, 2019 |
Title |
H3.3 phosphorylation promotes enhancer acetylation and lineage specification [ChIP-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
H3.3 phosphorylation promotes high levels of histone acetylation in mouse embryonic stem cells, which are central to the initiation of new transcription during lineage specification.
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Overall design |
Native ChIP analysis of H3K27ac in several mouse embryonic stem cell lines (Control and H3.3KO, HIRAKO, ATRXKO, DAXXKO). Native ChIP analysis of H3K64ac, H3K122ac, H3K4me1 in two embryonic stem cell lines (Control and H3.3KO). Crosslinking ChIP analysis of H3.3 (Control, ATRXKO and DAXXKO) and p300 (Control and H3.3KO). Native ChIP analysis of H3K27ac in embryoid bodies at Day 4 of differentiation (WT and H3.3KO and addback cells). All inputs sequenced.
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Contributor(s) |
Martire S, Gogate AA, Whitmill A, Tafessu A, Nguyen J, Teng YC, Tastemel M, Banaszynski LA |
Citation(s) |
31152160 |
Submission date |
May 16, 2018 |
Last update date |
Jun 09, 2019 |
Contact name |
Laura Banaszynski |
E-mail(s) |
Laura.banaszynski@utsouthwestern.edu
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Organization name |
UT Southwestern Medical Center
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Department |
Green Center for Reproductive Biology Sciences
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Street address |
5323 Harry Hines Blvd
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City |
Dallas |
State/province |
TX |
ZIP/Postal code |
75390-8511 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (58)
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This SubSeries is part of SuperSeries: |
GSE114551 |
H3.3 phosphorylation promotes enhancer acetylation and lineage specification |
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Relations |
BioProject |
PRJNA471722 |
SRA |
SRP147914 |