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Status |
Public on Sep 28, 2017 |
Title |
MYCL and EP400 are required for Max and MCPyV mediated gene activation |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
To determine if MYCL or EP400 knockdown would affect Max target genes in Merkel cell carcinoma cell line MKL-1, we performed RNA-seq analyses of MKL-1 cells inducibly expressing shMYCL and two different EP400 shRNA -2, -3 and compared to ChIP-seq data using BETA analyses.
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Overall design |
MYCL or EP400 was inducibly reduced with shRNA in MKL-1 cells to analyze gene regulation.
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Contributor(s) |
Cheng J |
Citation(s) |
29028833 |
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Submission date |
Jun 19, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Jingwei Cheng |
E-mail(s) |
jingweic@gmail.com
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Phone |
617-632-4797
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Organization name |
Dana-Farber Cancer Institute
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Department |
Medical Oncology
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Lab |
James A. DeCaprio
|
Street address |
450 Brookline Ave
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
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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: |
GSE69878 |
MCPyV ST activates Max target genes by recruiting TRRAP/EP400 complex |
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Relations |
BioProject |
PRJNA390939 |
SRA |
SRP109645 |