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Status |
Public on Oct 24, 2018 |
Title |
SUMO safeguards somatic and pluripotent cell identities by enforcing distinct chromatin states [SUMO-ChIP-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Mouse embryonic fibroblasts (MEFs) were generated from Ubc9fl/- and Ubc9+/+ embryos (E13.5). MEFs were treated with tamoxifen for six days to cause CreERT2 activation, and induce Ubc9 floxed allele deletion. We determined the ChIP-seq profiles of SUMO-1 and SUMO-2 using chromatin of wild-type MEFs Ubc9+/+ and of the corresponding Ubc9 KO MEFs which are entirely depleted for sumoylation. The analysis revealed the nearly complete absence of genome-wide binding of SUMO-1 and SUMO-2 in Ubc9-/- MEFs, attesting for antibody specificities.
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Overall design |
One replicate per condiition and mark
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Contributor(s) |
Cossec J, Theurillat I, Dejean A |
Citation(s) |
30401455 |
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Submission date |
Jun 15, 2018 |
Last update date |
Mar 21, 2019 |
Contact name |
Claudia Chica |
Organization name |
Institut Pasteur
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Lab |
Biostatistics and Bioinformatics Hub
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Street address |
25-28 Rue du Dr Roux
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City |
Paris |
ZIP/Postal code |
75015 |
Country |
France |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA476248 |
SRA |
SRP150597 |