Granberg, Fredrik
- Uppsala University
Abstract
In cell lines harbouring inducible adenovirus E1A genes, the cytotoxicity of wild type E1A was manifested by poor and subsiding expression of the E1A protein during prolonged induction. In contrast, cells expressing E1A deleted in the C-terminal binding protein (CtBP)-interaction domain (E1A Delta CID) demonstrated high levels of expression for extended time. Microarray analyses of host cell gene expression demonstrated that approximately 70% of the regulated genes were increased upon E1A induction and that the majority of E1A-regulated genes were similarly regulated by wild type E1A and E1A Delta CID. However, for 29 genes, regulation by wild type E1A and E1A Delta CID were different. Consistent with the altered transforming capacity of E1A unable to bind CtBP, genes involved in tumour cell progression and growth suppression were found among the differently regulated genes. Moreover, promoter sequences of genes up regulated by wild type E1A and/or repressed by E1A Delta CID demonstrated a higher prevalence of potential binding sites for the CtBP-targeted transcription factors Ets, Ikaros and/or partial derivative EF1/ZEB, suggesting that the failure to block CtBP-repression contributed to the "hyper-transforming" phenotype of E1A Delta CID. Since E1A Delta CID also specifically activated host cell gene expression, we find it likely that additional, possibly CtBP-independent, mechanisms contribute to the altered phenotype of E1A Delta CID-expressing cells. (c) 2005 Elsevier B.V. All rights reserved.
Keywords
adenovirus; E1A; CtBP; transcription; microarray
Published in
Virus Research
2005, volume: 113, number: 1, pages: 51-63
Publisher: ELSEVIER
SLU Authors
UKÄ Subject classification
Microbiology in the medical area
Publication identifier
- DOI: https://doi.org/10.1016/j.virusres.2005.04.015
Permanent link to this page (URI)
https://res.slu.se/id/publ/111962