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Status |
Public on Nov 08, 2014 |
Title |
Genome-wide maps of Scl/TAL1 in human erythroid cells. |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
ChIP-Seq experiments using an Scl/TAL1 antibody were carried out in primary erythroid cells cultured from two individuals of Caucasian origin. ChIP-Seq libraries were prepared from two biological replicates for each individual. ChIP DNA was processed for Illumina High-throughput sequencing according to Illumina protocol. By obtaining over four billion bases of sequence from chromatin immunoprecipitated DNA from each experiments, we generated a high-resolution map of Scl/TAL1 genomic targets in human erythroid cells. We find that WGATAR and the combinatorial CTG(n9)GATA are the most significant motifs responsible for the chromatin occupancy by Scl/TAL1. In addition, other motifs are also significantly enriched at the Scl/TAL1 targets. Amongst these were binding sites for known TFs (Sp/XKLF, RUNX1, NFE2). We next investigated how many of these targets varied between these two individuals. We find that 0.8% of Scl/TAL1 binding regions differ significantly between the two individuals.
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Overall design |
We have compared the genome-wide occupancy of Scl/TAL1 in erythroid cells between two different individuals
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Contributor(s) |
De Gobbi M, Lower KM, Hughes JR, Gibbons RR, Higgs DR |
Citation missing |
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Submission date |
Nov 19, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Richard J Gibbons |
E-mail(s) |
richard.gibbons@imm.ox.ac.uk
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Phone |
+441865222632
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Fax |
+441865222500
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URL |
http://www.imm.ox.ac.uk/wimm-research/molhaem/richard-gibbons
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Organization name |
Weatherall Institute of Molecular Medicine
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Department |
MRC Molecular Haematology Unit
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Lab |
Gibbons
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Street address |
John Radcliffe Hospital,
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City |
Oxford |
State/province |
Oxon |
ZIP/Postal code |
OX3 9DU |
Country |
United Kingdom |
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Platforms (1) |
GPL9115 |
Illumina Genome Analyzer II (Homo sapiens) |
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Samples (4)
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Relations |
BioProject |
PRJNA181274 |
SRA |
SRP017241 |