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Status |
Public on Sep 01, 2013 |
Title |
Global analysis of NFATc1 binding and histone marks in VEGF-activated endothelial cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We performed the newly mapping of genome-wide NFATc1 binding events in VEGF-stimulated primary cultured endothelial cells, by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq). Combined NFATc1 ChIP-seq profile and the epigenetic histone marks revealed that predominant NFATc1-occupied peaks were overlapped with promoter marking but not silencer marking. DNA microarrays with NFATc1 expression or knockdown indicated the predominant NFATc1 binding targets were correlated with induced patterns.
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Overall design |
Examination of NFATc1 and two different histone marks in HUVEC in the presence/absense of VEGF.
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Contributor(s) |
Suehiro J, Kanki Y, Miura M, Manabe Y, Aburatani H, Kodama T, Minami T |
Citation(s) |
25157100 |
Submission date |
Jul 31, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Jun-ichi Suehiro |
Organization name |
Kyorin University School of Medicine
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Department |
Department of Pharmacology and Toxicology
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Street address |
6-20-2, Shinkawa
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City |
Mitaka |
State/province |
Tokyo |
ZIP/Postal code |
181-8611 |
Country |
Japan |
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Platforms (1) |
GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE49429 |
Genome-wide approaches reveal functional VEGF-inducible NFATc1 binding to the angiogenesis-related genes in endothelium |
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Relations |
BioProject |
PRJNA215174 |
SRA |
SRP028803 |