NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE10863 Query DataSets for GSE10863
Status Public on Mar 18, 2008
Title microRNA-155 is an Epstein-Barr Virus induced gene that modulates EBV-regulated gene expression (EBV infection)
Organism Homo sapiens
Experiment type Expression profiling by array
Summary The cellular microRNA, miR-155 has been shown to be involved in lymphocyte activation and is expressed in EBV infected cells displaying type III latency gene expression but not type I latency gene expression. We show here that the elevated levels of miR-155 in type III latency cells is due to EBV gene expression and not epigenetic differences in cell lines tested and we show that expression in EBV infected cells requires a conserved AP-1 element in the miR-155 promoter. Gene expression analysis was carried out in a type I latency cell line transduced with a miR-155 expressing retrovirus. This analysis identified both miR-155 suppressed and induced cellular mRNAs and suggested that in addition to direct targeting of 3’ UTRs, miR-155 alters gene expression in part through the alteration of signal transduction pathways. 3’ UTR reporter analysis of predicted miR-155 target genes identified the transcriptional regulatory genes, BACH1, ZIC3, HIVEP2, CEBPB, ZNF652, ARID2, and SMAD5 as miR-155 targets. Western blot analysis of the most highly suppressed of these, BACH1, showed lower expression in cells transduced with a miR-155 retrovirus. Inspection of the promoters from genes regulated in EBV infected cells and in cells infected with a miR-155 retrovirus identified potential binding sequences for BACH1 and ZIC3. Together, these experiments suggest that the induction of miR-155 by EBV contributes to EBV mediated signaling in part through the modulation of transcriptional regulatory factors.
Keywords: Gene expression analysis in EBV positive vs EBV negative cells
 
Overall design Two RNA preps from the EBV negative Burkitt's lymphoma cell line, BL41, and two RNA preps from EBV converted BL41 cells were prepared. In each two color array, EBV positive BL41s were run with EBV negative BL41s. RNA prep set 1 were run in duplicate, RNA prep set 2 were run in duplicate and all four of these combinations were run as dye swaps for a total of eight arrays.
 
Contributor(s) Yin Q, McBride J, Fewell C, Lacey M, Wang X, Lin Z, Cameron J, Flemington EK
Citation(s) 18367535
Submission date Mar 17, 2008
Last update date Feb 22, 2018
Contact name Erik K Flemington
E-mail(s) eflemin@tulane.edu
Phone 504 988-1167
Organization name Tulane Health Sciences Center
Department Pathology
Street address 1430 Tulane Ave., SL79
City New Orleans
State/province LA
ZIP/Postal code 70112
Country USA
 
Platforms (1)
GPL4133 Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Feature Number version)
Samples (8)
GSM274844 BL30 (B95-8) vs BL30 – RNA pair 1
GSM274845 BL30 (B95-8) vs BL30 – RNA pair 2
GSM274846 BL30 (B95-8) vs BL30 – RNA pair 1 – Repeat
This SubSeries is part of SuperSeries:
GSE10868 microRNA-155 is an Epstein-Barr Virus induced gene that modulates Epstein Barr virus regulated gene expression pathways
Relations
BioProject PRJNA108885

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

Supplementary file Size Download File type/resource
GSE10863_RAW.tar 120.1 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap