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Series GSE102360 Query DataSets for GSE102360
Status Public on Dec 01, 2017
Title Selective expression of the transcription elongation factor Eleven Nineteen Lysine-rich Leukemia 3 (ELL3) in actiavted B lymphocytes drives rapid B cell proliferation
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary To identify novel targets of the transcriptional repressor that functions to extinguish the B cell phenotype during terminal plasma cell differentiation, we assessed PRDM1 bound sequences through ChIP-Seq. We prepared PRDM1-enriched chromatin from two PRDM1 positive mutiple myeloma cell lines, U266 and NCI-H929. At least 5 PRDM1- or IgG enrichments were performed per cell line and pooled into the two respective conditions per cell line. The U226 and NCI-H929 revealed respectively, 574 and 2887 association peaks were indentified per cell line. Both cell lines displayed an intense peak at the ELL3 loci, suggesting PRDM1 association. This was validated by ChIP followed by qPCR, confirming PRDM1 association.
 
Overall design Examination of PRDM1 binding sites in two Multiple Myeloma cell lines
 
Contributor(s) Alexander LM, Wright KL
Citation(s) 28858629
Submission date Aug 08, 2017
Last update date Jul 25, 2021
Contact name Kenneth Wright
E-mail(s) ken.wright@moffitt.org
Organization name H Lee Moffitt Cancer Center
Department Immunology
Street address 12902 Magnolia Dr
City Tampa
State/province Florida
ZIP/Postal code 33612
Country USA
 
Platforms (1)
GPL15456 Illumina HiScanSQ (Homo sapiens)
Samples (2)
GSM2735455 Input ChIP-Seq
GSM2735456 PRDM1 ChIP-Seq
Relations
BioProject PRJNA397567
SRA SRP115027

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
GSE102360_RAW.tar 430.0 Kb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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