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Status |
Public on Aug 22, 2017 |
Title |
Transcription factors enriched in tumor-associated enhancers in VHL-deficient ccRCC |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
VHL loss is the most common genetic alteration event in ccRCC. We profiled histone modifications from VHL-deficient ccRCC primary tumors and cell lines. We show that ccRCCs exhibit a pervasive gain of enhancers around hypoxic and metabolic transcriptional targets. Motif analysis using HOMER revealed significant enrichment of AP-1, ETS, NFĸB and HIFα in tumor enhancers. We generated ChIP-seq binding data for c-Jun, ETS1, NFĸB, and P300, a histone acetyltransferase, in 786-O cells. ChIP-seq profiles of HIF2α and HIF1β in 786-O were already generated previously (GSE34871)
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Overall design |
Transcription factor ChIP-Seq in ccRCC cell lines
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Contributor(s) |
Yao X, Tan P |
Citation(s) |
28893800 |
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Submission date |
Aug 26, 2016 |
Last update date |
Jul 25, 2021 |
Contact name |
Xiaosai Yao |
E-mail(s) |
xiaosai.yao@gmail.com, yao.xiaosai@gene.com
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Phone |
+65 68088271
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Organization name |
Genome Institute of Singapore
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Street address |
60 Biopolis Street, Genome, #02-01
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City |
Singapore |
ZIP/Postal code |
138672 |
Country |
Singapore |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE86095 |
VHL deficiency drives enhancer activation of oncogenes in clear cell renal cell carcinoma |
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Relations |
BioProject |
PRJNA340241 |
SRA |
SRP083009 |