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Gene set: P53_DOWN_KANNAN (C2:PERT:0014)
Standard nameP53_DOWN_KANNAN
Systematic nameC2:PERT:0014
Brief descriptionTarget genes down regulated by p53
CategoryC2: Curated
Sub-categoryPERT: Experimental pertuberation
Full description or Abstract

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The transcriptional program regulated by the tumor suppressor
p53 was analysed using oligonucleotide microarrays. A human lung
cancer cell line that expresses the temperature sensitive murine
p53 was utilized to quantitate mRNA levels of various genes at
different time points after shifting the temperature to 32 degrees
C. Inhibition of protein synthesis by cycloheximide (CHX) was
used to distinguish between primary and secondary target genes
regulated by p53. In the absence of CHX, 259 and 125 genes were
up or down-regulated respectively; only 38 and 24 of these genes
were up and down-regulated by p53 also in the presence of CHX
and are considered primary targets in this cell line. Cluster
analysis of these data using the super paramagnetic clustering
(SPC) algorithm demonstrate that the primary genes can be distinguished
as a single cluster among a large pool of p53 regulated genes.
This procedure identified additional genes that co-cluster with
the primary targets and can also be classified as such genes.
In addition to cell cycle (e.g. p21, TGF-beta, Cyclin E) and apoptosis
(e.g. Fas, Bak, IAP) related genes, the primary targets of p53
include genes involved in many aspects of cell function, including
cell adhesion (e.g. Thymosin, Smoothelin), signaling (e.g. H-Ras,
Diacylglycerol kinase), transcription (e.g. ATF3, LISCH7), neuronal
growth (e.g. Ninjurin, NSCL2) and DNA repair (e.g. BTG2, DDB2).
The results suggest that p53 activates concerted opposing signals
and exerts its effect through a diverse network of transcriptional
changes that collectively alter the cell phenotype in response
to stress. 
Publication URL11402317
External linksna
Keywords & MeSH headingsNeoplastic,RNA,Gene Expression Profiling,Lung Neoplasms/genetics/metabolism,Oligonucleotide Array Sequence Analysis,Messenger/genetics,Human,Protein p53,Support,Tumor Cells,Trans-Activation (Genetics),Cycloheximide/pharmacology,genetics,Mice,Gene Expression Regulation,physiology,Protein Synthesis Inhibitors/pharmacology,Cultured,Cluster Analysis
OrganismHuman
Contributed byBroad Institute
Source platformHu6800
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Genes

19 genes, 19 accessions (Toggle view)

AccessionGeneTitleLinks
ARL4A
CDC6
ARL5
BIRC3
APBA2
CPM
MAC30
PURA
CCNE1
EIF4A1
GOS2
COL18A1
CXADR
INA
PPAT
PMP22
C4orf9
FOSL2
BRCA1


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