|
Status |
Public on Aug 18, 2013 |
Title |
Addiction of t(8;21) and inv(16) AML to native RUNX1 [ChIP-Seq data] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Cancer cells maintain a sensitive balance between growth-promoting oncogenes and apoptosis inhibitors. We show that WT RUNX1 is required for survival of t(8;21)-Kasumi-1 and inv(16)-ME-1 AML cell lines. The malignant AML phenotype is sustained by a delicate AML1-ETO/RUNX1 balance that involves competition for common DNA binding sites regulating a subset of AML1-ETO/RUNX1 targets.
|
|
|
Overall design |
Genomewide sequencing data is included herein: Transcription factors RUNX1 c-terminus and n-terminus which is shared with AML1-ETO were profiled independently), AML1-ETO and AP4 were profiled using ChIP-Seq in Kasumi-1 cells, as well as control ChIP-Seq experiments of non immune serum. Two replicates were performed for each transcription factor profiling and control experiment.
|
|
|
Contributor(s) |
Ben Ami O, Friedman D |
Citation(s) |
24055056 |
|
Submission date |
Apr 03, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Yoram Groner |
E-mail(s) |
yoram.groner@weizmann.ac.il
|
Organization name |
Weizmann institute
|
Department |
Molecular Genetics
|
Street address |
234 Herzl St.
|
City |
Rehovot |
ZIP/Postal code |
76100 |
Country |
Israel |
|
|
Platforms (1) |
GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
|
Samples (12)
|
|
This SubSeries is part of SuperSeries: |
GSE45748 |
Addiction of t(8;21) and inv(16) AML to native RUNX1 |
|
Relations |
BioProject |
PRJNA196162 |
SRA |
SRP020494 |