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Status |
Public on Apr 21, 2016 |
Title |
Epigenetic Profiles Signify Cell Fate Plasticity in Unipotent Spermatogonial Stem and Progenitor Cells (ChIP-Seq) |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Mammalian spermatogonial stem cells (SSCs) spontaneously convert to multipotent adult spermatogonial-derived stem cells (MASCs) during in vitro expansion. Here, we examine the epigenetic signature of SSCs and MASCs, identifying bivalent histone H3-lysine4 and -lysine27 trimethylation at somatic gene promoters in SSCs and an ESC-like promoter chromatin state in MASCs.
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Overall design |
Examination of histone modifications K4me3, K27me3, and K27ac in different cell types.
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Contributor(s) |
Liu Y, Rafii S |
Citation(s) |
27117588 |
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Submission date |
Feb 19, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Ying Liu |
E-mail(s) |
yil2004@med.cornell.edu
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Organization name |
Weill Cornell Medical College
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Department |
Medicine
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Street address |
1300 York Ave
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10021 |
Country |
USA |
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Platforms (1) |
GPL15103 |
Illumina HiSeq 1000 (Mus musculus) |
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Samples (33)
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Relations |
BioProject |
PRJNA312674 |
SRA |
SRP070585 |