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Series GSE45738 Query DataSets for GSE45738
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)
GSM1113427 Kasumi_RUNX1_1
GSM1113428 Kasumi_RUNX1_2
GSM1113429 Kasumi_AML1_ETO_1
This SubSeries is part of SuperSeries:
GSE45748 Addiction of t(8;21) and inv(16) AML to native RUNX1
Relations
BioProject PRJNA196162
SRA SRP020494

Download family Format
SOFT formatted family file(s) SOFTHelp
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE45738_RAW.tar 4.3 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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