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Status |
Public on Oct 17, 2013 |
Title |
Dynamics of Sox2 and Esrrb occupancy during the differentiation of embryonic stem cells into trophoblast stem cells. |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To understand the mechanism underlying the versatility in transcriptional regulation by Sox2 and Esrrb, we compared genome-wide binding sites of Sox2 and Esrrb in embryonic stem (ES) cells and trophoblast stem (TS) cells by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq).
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Overall design |
A tetracycline-inducible Oct3/4 knockout ES cell line ZHBTc4 was treated with Tet for 4 days in the presence of FGF4 and mouse embryonic fibroblasts (MEFs).
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Contributor(s) |
Adachi K, Nikaido I, Ura H, Ueda HR, Niwa H |
Citation(s) |
24120664 |
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Submission date |
Apr 07, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Itoshi NIKAIDO |
E-mail(s) |
itoshi.nikaido@riken.jp
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Organization name |
RIKEN
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Department |
Center for Biosystems Dynamics Research
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Lab |
Laboratory for Bioinformatics Research
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Street address |
2-1 Hirosawa
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City |
Wako |
State/province |
Saitama |
ZIP/Postal code |
351-0198 |
Country |
Japan |
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Platforms (1) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
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Samples (11)
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This SubSeries is part of SuperSeries: |
GSE28455 |
Sox2-regulatory networks in embryonic and trophoblast stem cells |
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Relations |
SRA |
SRP006420 |
BioProject |
PRJNA143235 |