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Status |
Public on Mar 01, 2017 |
Title |
Genome-wide analysis of histone modifications during neutrophilic granulopoiesis following ELF-MF exposure |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To address whether ELF-MF influences the epigenetic landscape in differentiating haematopoietic cells, we performed an in vitro haematopoietic differentiation under powerline-simulating ELF-MF exposure (50 Hz, 1 mT, 5’ on/10’ off) in comparison to sham exposure (50 Hz, 7 µT, 5’ on/10’ off) or no exposure. We differentiated CD34+ cells (allcells, CB008F, lot: CBC121009M) isolated from human cord blood into the neutrophilic lineage, and performed ChIP combined with next generation sequencing for the histone modifications H3K4me2 and H3K27me3 before (t0) and after 5 days (t5) of differentiation. Genome-wide profiling of active and repressive histone modifications did not reveal significant alterations. However, ELF MF exposure has an influence on the robustness of the epigenetic landscape during global chromatin programming of granulopoiesis. Our data suggests that ELF MF has a stochastic effect on the epigenetic landscape of individual cells.
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Overall design |
H3K4me2 and H3K27me3 profiles from CD34+ cells, sham and ELF-MF exposed neutrophilic progenitors after 5 days of differentiation in duplicates and not-exposed neutrophlic progenitors after 5 days (one replicate) analyzed by deep sequencing.
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Contributor(s) |
Manser M, Sater M, Schmid C, Noreen F, Murbach M, Schurmann D, Schar P |
Citation(s) |
28266526 |
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Submission date |
Aug 12, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Primo Schaer |
E-mail(s) |
primo.schaer@unibas.ch
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Organization name |
University of Basel
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Department |
Department of Biomedicine
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Lab |
Genome Plasticity Laboratory
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Street address |
Mattenstrasse 28
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City |
Basel |
ZIP/Postal code |
4058 |
Country |
Switzerland |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (16)
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Relations |
BioProject |
PRJNA338799 |
SRA |
SRP081575 |