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Status |
Public on Sep 15, 2015 |
Title |
Epigenetic profiling of Juvenile Idiopathic Arthritits (JIA) patients |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
With H3K27ac chromatin immunoprecipitation we identified a disease-specific, inflammation-associated, (super-)enhancer signature in JIA patient synovial fluid-derived CD4+ memory/effector T cells. This signature consists of unique pathogenesis-associated epigenetic changes which extend beyond general T cell activation-induced alterations, indicating that disease-specific (super-)enhancers contribute to JIA pathogenesis. In addition, our analysis shows that there is a profound enrichment of JIA-related SNPs in (super-)enhancers in JIA patients compared to controls, illustrating the importance of these non-coding regions for disease pathogenesis.
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Overall design |
H3K27ac ChIP-sequencing of CD4+ memory/effector T cells derived from peripheral blood (PB) from healthy controls (HC) and PB or synovial fluid (SF) from JIA patients.
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Contributor(s) |
. van Loosdregt J, Peeters JG, Vervoort SJ |
Citation(s) |
26387944 |
Submission date |
Jul 31, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Janneke Peeters |
E-mail(s) |
j.g.c.peeters-7@umcutrecht.nl
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Organization name |
UMC Utrecht
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Street address |
Heidelberglaan 100
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City |
Utrecht |
ZIP/Postal code |
3584CX |
Country |
Netherlands |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (15)
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This SubSeries is part of SuperSeries: |
GSE71597 |
Epigenetic profiling and RNA-sequencing of Juvenile Idiopathic Arthritits (JIA) patients |
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Relations |
BioProject |
PRJNA291598 |
SRA |
SRP061882 |