Impact of the interaction between adenovirus E1A and CtBP on host cell gene expression

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

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