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Status |
Public on Jan 01, 2014 |
Title |
ChIP-seq analysis of chromatin state plasticity in primary human adult erythroid progenitor cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We report a computational approach for investigation of chromatin state plasticity. We applied this approach to investigate an ENCODE ChIP-seq dataset profiling the genome-wide distribution of H3K27me3 in 19 human cell lines. We found that high plasticity regions (HPRs) can be divided into two functionally and mechanistically distinct groups, consisting of CpG island proximal and distal regions. We identified cell-type specific regulators correlating with H3K27me3 patterns at distal HPRs in ENCODE cell lines. Furthermore, we applied this approach to investigate mechanisms for poised enhancer establishment in primary human erythroid precursors. We predicted and validated a previously unrecognized role of TAL1 in modulating H3K27me3 patterns through interaction with additional cofactors, such as GFI1B. Our integrative approach provides mechanistic insights into chromatin state plasticity and is broadly applicable to other epigenetic marks.
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Overall design |
Analysis of genomic occupancy of H3K27me3, H3K27ac, GATA1, TAL1/SCL and GFI1B in primary adult human proerythroblasts by ChIP-seq.
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Contributor(s) |
Pinello L, Xu J, Orkin SH, Yuan G |
Citation(s) |
24395799 |
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Submission date |
Dec 03, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Jian Xu |
E-mail(s) |
[email protected]
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Phone |
9015955208
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Organization name |
St. Jude Children's Research Hospital
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Department |
Pathology
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Street address |
262 Danny Thomas Place, MS 345
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City |
Memphis |
State/province |
Tennessee |
ZIP/Postal code |
38105 |
Country |
USA |
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Platforms (2) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
GPL14761 |
Helicos HeliScope (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA230472 |
SRA |
SRP033440 |