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Status |
Public on Jun 13, 2013 |
Title |
Effect of ETV1 knockdown on genome wide AR binding in LNCaP Cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Translocation of ETS transcription factors including ERG and ETV1 occur in half of all prostate cancers. LNCaP cells harbor an ETV1 translocation. We performed ChIP-Seq analysis to determine the role of ETV1 on AR binding. The localization of enhancers were determined by H3K4me1 ChIP-Seq.
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Overall design |
To determine ETV1 and H3K4me1 localization, logarithmically growing cells
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Contributor(s) |
Chen Y, Sawyers CL |
Citation(s) |
23817021 |
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Submission date |
May 20, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Yu Chen |
E-mail(s) |
cheny1@mskcc.org
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Phone |
646-888-3356
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Organization name |
Memorial Sloan Kettering Cancer Center
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Department |
Human Oncology and Pathogenesis Program
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Lab |
Chen
|
Street address |
1275 York Ave, Box 20
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
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Samples (5)
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This SubSeries is part of SuperSeries: |
GSE47220 |
ETS factors reprogram the androgen receptor cistrome and prime prostate tumorigenesis in response to PTEN loss |
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Relations |
BioProject |
PRJNA203679 |
SRA |
SRP022924 |