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Cell target genes of Epstein-Barr virus transcription factor EBNA-2: induction of the p55alpha regulatory subunit of PI3-kinase and its role in survival of EREB2.5 cells.
- Source :
-
The Journal of general virology [J Gen Virol] 2006 Oct; Vol. 87 (Pt 10), pp. 2859-2867. - Publication Year :
- 2006
-
Abstract
- Microarray analysis covering most of the annotated RNAs in the human genome identified a panel of genes induced by the Epstein-Barr virus (EBV) EBNA-2 transcription factor in the EREB2.5 human B-lymphoblastoid cell line without the need for any intermediate protein synthesis. Previous data indicating that PIK3R1 RNA (the alpha regulatory subunit of PI3-kinase) was induced were confirmed, but it is now shown that it is the p55alpha regulatory subunit that is induced. Several EBV-immortalized lymphoblastoid cell lines were shown to express p55alpha. Expression of PI3-kinase p85 regulatory and p110 catalytic subunits was not regulated by EBNA-2. Proliferation of EREB2.5 lymphoblastoid cells was inhibited by RNAi knock-down of p55alpha protein expression, loss of p55alpha being accompanied by an increase in apoptosis. p55alpha is thus a functional target of EBNA2 in EREB2.5 cells and the specific regulation of p55alpha by EBV will provide an opportunity to investigate the physiological function of p55alpha in this human cell line.
- Subjects :
- Apoptosis
Cell Line
Cell Survival
Enzyme Induction
Gene Expression Profiling
Humans
Oligonucleotide Array Sequence Analysis
Phosphatidylinositol 3-Kinases chemistry
Protein Subunits biosynthesis
Protein Subunits genetics
RNA Interference
Epstein-Barr Virus Nuclear Antigens metabolism
Gene Expression Regulation
Herpesvirus 4, Human metabolism
Phosphatidylinositol 3-Kinases biosynthesis
Phosphatidylinositol 3-Kinases genetics
Transcription Factors metabolism
Viral Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0022-1317
- Volume :
- 87
- Issue :
- Pt 10
- Database :
- MEDLINE
- Journal :
- The Journal of general virology
- Publication Type :
- Academic Journal
- Accession number :
- 16963743
- Full Text :
- https://doi.org/10.1099/vir.0.82128-0