Identification of genes differentially expressed as result of adenovirus type 5- and adenovirus type 12-transformation
| Autor: | Lindsay J Georgopoulos, Paul Kellam, G. Eric Blair, Janet Strath |
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| Jazyk: | angličtina |
| Rok vydání: | 2009 |
| Předmět: |
Candidate gene
lcsh:QH426-470 Bioinformatics Adenoviridae Infections viruses lcsh:Biotechnology Biology medicine.disease_cause lcsh:TP248.13-248.65 Gene expression Transcriptional regulation medicine Genetics Animals Neoplastic transformation Rats Wistar Gene Cell Line Transformed Oligonucleotide Array Sequence Analysis Regulation of gene expression 08 Information And Computing Sciences Adenoviruses Human 11 Medical And Health Sciences 06 Biological Sciences Cell Transformation Viral Molecular biology Phenotype Cell biology Rats lcsh:Genetics Gene Expression Regulation RNA Carcinogenesis Biotechnology Research Article |
| Zdroj: | BMC Genomics, Vol 10, Iss 1, p 67 (2009) BMC Genomics BMC Genomics, 10 p. 67. (2009) |
| ISSN: | 1471-2164 |
| Popis: | Background Cells transformed by human adenoviruses (Ad) exhibit differential capacities to induce tumours in immunocompetent rodents; for example, Ad12-transformed rodent cells are oncogenic whereas Ad5-transformed cells are not. The E1A gene determines oncogenic phenotype, is a transcriptional regulator and dysregulates host cell gene expression, a key factor in both cellular transformation and oncogenesis. To reveal differences in gene expression between cells transformed with oncogenic and non-oncogenic adenoviruses we have performed comparative analysis of transcript profiles with the aim of identifying candidate genes involved in the process of neoplastic transformation. Results Analysis of microarray data revealed that a total of 232 genes were differentially expressed in Ad12 E1- or Ad5 E1-transformed BRK cells compared to untransformed baby rat kidney (BRK) cells. Gene information was available for 193 transcripts and using gene ontology (GO) classifications and literature searches it was possible to assign known or suggested functions to 166 of these identified genes. A subset of differentially-expressed genes from the microarray was further examined by real-time PCR and Western blotting using BRK cells immortalised by Ad12 E1A or Ad5 E1A in addition to Ad12 E1- or Ad5 E1-transformed BRK cells. Up-regulation of RelA and significant dysregulation of collagen type I mRNA transcripts and proteins were found in Ad-transformed cells. Conclusion These results suggest that a complex web of cellular pathways become altered in Ad-transformed cells and that Ad E1A is sufficient for the observed dysregulation. Further work will focus on investigating which splice variant of Ad E1A is responsible for the observed dysregulation at the pathway level, and the mechanisms of E1A-mediated transcriptional regulation. |
| Databáze: | OpenAIRE |
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