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Status |
Public on Aug 01, 2012 |
Title |
H4K20me1 contributes to downregulation of X-linked genes for Caenorhabditis elegans dosage compensation |
Organism |
Caenorhabditis elegans |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We compared the pattern of H4K20me1 at the L3 stage in wild-type and set-4 mutants by ChIP-seq. In wild-type, H4K20me1 levels on the X chromosome are higher than on autosomes. In set-4 mutants, this difference is lost.
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Overall design |
ChIP-seq of H4K20me1 at the L3 stage in wild-type and set-4 mutant L3 larvae.
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Contributor(s) |
Ahringer J |
Citation(s) |
23028348 |
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Submission date |
Jul 31, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Przemyslaw Aleksander Stempor |
Organization name |
University of Cambridge
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Department |
The Gurdon Institute
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Lab |
Ahringer Lab
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Street address |
Tennis Court Road
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City |
Cambridge |
State/province |
United Kingdom |
ZIP/Postal code |
CB2 1QN |
Country |
United Kingdom |
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Platforms (1) |
GPL13657 |
Illumina HiSeq 2000 (Caenorhabditis elegans) |
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Samples (3) |
GSM979032 |
H4K20me1 ChIP-seq of wild-type |
GSM979033 |
H4K20me1 ChIP-seq of set-4 mutant, rep1 |
GSM979034 |
H4K20me1 ChIP-seq of set-4 mutant, rep2 |
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Relations |
BioProject |
PRJNA171711 |
SRA |
SRP014640 |