NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE7892 Query DataSets for GSE7892
Status Public on Sep 01, 2009
Title Global analysis of gene expression in MEF cells and villi enterocytes expressing SV40 T antigens
Organism Mus musculus
Experiment type Expression profiling by array
Summary SV40 transforms cells through the action of two oncoproteins, large T antigen and small t antigen. Small t antigen targets phosphatase PP2A, while large T antigen stimulates cell proliferation and survival by action on multiple proteins, including the tumor suppressors Rb and p53. Large T antigen also binds components of the transcription initiation complex and several transcription factors. We examined global gene expression in SV40-transformed mouse embryo fibroblasts, and in enterocytes obtained from transgenic mice. SV40 transformation alters the expression of approximately 800 cellular genes in both systems. Much of this regulation is observed in both MEFs and enterocytes and is consistent with T antigen action on the Rb-E2F pathway. However, the regulation of many genes is cell-type specific, suggesting that unique signaling pathways are activated in different cell types upon transformation, and that the consequences of SV40 transformation depends on the type of cell targeted.
Keywords: comparative genomic hybridization
 
Overall design We used the Agilent Mouse cDNA (G4104A) array for these experiments. For the MEF microarrays, we used a dye-flip reference design (Churchill GA, 2002, Nature Genetics, Vol. 32, p.490-495) to compare a pool of MEF total RNA to three independent T antigen MEF cell lines. Cells were grown to two days post-confluence and harvested. For the mouse small intestine microarrays, we used three different intestinal preparations: Whole, Villi and Vlcm in a replicated dye-flip design (Churchill GA) using three (Vlcm) or four (Whole and Villi) T+ mice and the same number of their wild-type littermates for each intestinal preparation.
 
Contributor(s) Cantalupo PG
Citation(s) 19201438
Submission date May 24, 2007
Last update date Mar 16, 2012
Contact name Daniel Clark
Organization name University of Pittsburgh
Street address 3501 Terrace St.
City Pittsburgh
ZIP/Postal code 15213
Country USA
 
Platforms (2)
GPL871 Agilent Mouse cDNA Microarray (G4104A) [layout A]
GPL872 Agilent Mouse cDNA Microarray (G4104A) [layout B]
Samples (30)
GSM194123 MEFT clone 2, bio rep 1, TAg Cy5/wt Cy3
GSM194124 MEFT clone 2, bio rep 1, dyeflip TAg Cy3/wt Cy5
GSM194125 MEFT clone 4, bio rep 2, TAg Cy5/wt Cy3
Relations
BioProject PRJNA99935

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
GSE7892_RAW.tar 92.6 Mb (http)(custom) TAR (of TSV)
GSE7892_Readme.txt 2.9 Kb (ftp)(http) TXT
Processed data included within Sample table

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