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PMID: 9285562 Published · ppublish English Journal Article

SAGE transcript profiles for p53-dependent growth regulation.

Oncogene ·Vol. 15 ·No. 9 ·1997-08-28 ·Pages 1079-85

Madden SL, Galella EA, Zhu J, Bertelsen AH, Beaudry GA

Abstract

Serial analysis of gene expression (SAGE) allows for a quantitative, representative, and comprehensive profile of gene expression. We have utilized SAGE technology to contrast the differential gene expression profile in rat embryo fibroblast cells producing temperature-sensitive p53 tumor suppressor protein at permissive or non-permissive temperatures. Analysis of approximately 15,000 genes revealed that the expression of 14 genes (P < 0.001, > or = 0.03% abundance) was dependent on functional p53 protein, whereas the expression of three genes was significantly higher in cells producing non-functional p53 protein. Those genes whose expression was increased by functional p53 include RAS, U6 snRNA, cyclin G, EGR-1, and several novel genes. The expression of actin, tubulin, and HSP70 genes was elevated at the non-permissive temperature for p53 function. Interestingly, the expression of several genes was dependent on a non-temperature-sensitive mutant p53 suggesting altered transcription profiles dependent on specific p53 mutant proteins. These results demonstrate the utility of SAGE for rapidly and reproducibly evaluating global transcriptional responses within different cell populations.

MeSH Terms
Animals Cell Division/genetics Cell Line Cloning, Molecular/methods Embryo, Mammalian Fibroblasts/cytology,metabolism Gene Expression Regulation Genes, p53 Rats Reproducibility of Results Temperature Transcription, Genetic
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Madden S L
Department of Molecular & Cellular Biology, PharmaGenics, Inc., Allendale, NJ 07401, USA.
Galella E A
Zhu J
Bertelsen A H
Beaudry G A
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1997-08-28
Pages
1079-85
Language
English
Region
England
NLM ID
8711562
Subset
IM
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