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Status |
Public on Sep 21, 2015 |
Title |
Genome-wide map of H3K4me3 in HEK293 cells after PRDM9 expression |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
PRDM9 is a histone methyltransferase expressed in meiotic germ cells that determines the location of genetic recombination hotspots through binding of its allele-specific DNA binding domain. Here we characterize the genome-wide chromatin modification for two human PRDM9 alleles (A and C) in human cell lines. HEK293 cells were transfected with both alleles and an empty vector control. Resulting chromatin was subjected to H3K4me3 ChIP followed by high-throughput sequencing. We find that different PRDM9 allele largely modified chromatin in entirely different genomic regions in somatic cells determined by the protein's zinc-finger DNA binding domains. Many of the allele-specific peaks overlap sites of meiotic double-strand breaks found in vivo in human germ cells suggesting that transient expression of PRDM9 in somatic cells can reflect binding in vivo.
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Overall design |
Identify PRDM9-dependent H3K4me3 sites by comparing modified chromatin after expression of different human PRDM9 alleles in HEK293 cells.
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Contributor(s) |
Baker CL, Paigen K |
Citation(s) |
26368021 |
Submission date |
Apr 08, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Christopher Lee Baker |
E-mail(s) |
christopher.baker@jax.org
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Phone |
2072886365
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Organization name |
The Jackson Laboratory
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Department |
Research
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Street address |
600 Main Street
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City |
Bar Harbor |
State/province |
ME |
ZIP/Postal code |
04609 |
Country |
USA |
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Platforms (2) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (10)
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Relations |
BioProject |
PRJNA280610 |
SRA |
SRP057026 |