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Status |
Public on Jun 07, 2021 |
Title |
GATA6 defines endoderm fate by controlling chromatin accessibility during differentiation of human induced pluripotent stem cells [TF_ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Investigation of the role played by GATA6 in establishing the definitive endoderm chromatin accessbility profile. We used pluripotent stem cells as a model of early development. We derived GATA6-/- pluripotent cells with an inducible GATA6 or FOXA2 construct that permits exongenous GATA6 or FOXA2 cDNA expression upon supplementation of doxycycline. We differentiated GATA6+/+ and GATA6-/- (with and without doxycyline) cells to definitive endoderm and analyzed transcription factor binding profiles using CHIP-seq.
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Overall design |
Examination of GATA6, EOMES and FOXA2 binding profiles during definitive endoderm formation in the absence and presence of GATA6.
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Contributor(s) |
Heslop JA, Duncan SA |
Citation(s) |
34010638 |
Submission date |
Jan 04, 2021 |
Last update date |
Jun 07, 2021 |
Contact name |
Stephen A Duncan |
E-mail(s) |
duncanst@musc.edu
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Phone |
843-792-9104
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Organization name |
Medical University South Carolina
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Department |
Regenerative Medicine and Cell Biology
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Lab |
Duncan Lab
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Street address |
173 Ashley Avenue, BSB 6th Floor, Room 657A
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City |
Charleston |
State/province |
SC |
ZIP/Postal code |
29425 |
Country |
USA |
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Platforms (1) |
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Samples (11)
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This SubSeries is part of SuperSeries: |
GSE156021 |
GATA6 defines endoderm fate by controlling chromatin accessibility during differentiation of human induced pluripotent stem cells. |
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Relations |
BioProject |
PRJNA689593 |
SRA |
SRP300245 |