Genome-wide transcription program and expression of the Rta responsive gene of Epstein–Barr virus
Autor: | Mei-Ru Chen, Sheng-Wen Yeh, Yi-Ying Jeng, Chih-Chung Lu, Mei-Ying Liu, Tsuey-Ying Hsu, Ching-Hwa Tsai |
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Rok vydání: | 2006 |
Předmět: |
DNA Replication
Gene Expression Regulation Viral Gene expression cluster Herpesvirus 4 Human Transcription Genetic viruses Genome Viral Biology medicine.disease_cause Cell Line Immediate-Early Proteins Viral Proteins EBV Cell Line Tumor hemic and lymphatic diseases Virology Virus latency Gene expression medicine Humans DNA replication-dependent gene expression Rta responsive gene expression Gene Cell Line Transformed Oligonucleotide Array Sequence Analysis Regulation of gene expression Gene Expression Profiling medicine.disease Molecular biology Epstein–Barr virus Virus Latency Raji cell Gene expression profiling Viral replication Trans-Activators |
Zdroj: | Virology. 345:358-372 |
ISSN: | 0042-6822 |
DOI: | 10.1016/j.virol.2005.09.064 |
Popis: | Infection with Epstein–Barr virus (EBV) usually leads to a latent state in B lymphocytes. The virus can be reactivated through two viral transactivators, Zta and Rta, leading to a cascade of gene expression. An EBV DNA array was generated to analyze the pattern of transcription of the entire EBV genome under various conditions. Firstly, a complete set of temporal expression clusters of EBV genes was displayed by analyzing the array data of anti-IgG-induced Akata cells. In addition to assigning genes of unknown function to the various clusters, increasing expression of latent genes, including EBNA2, EBNA3A and EBNA 3C, was observed during virus replication. Secondly, gene expression independent of viral DNA replication was analyzed in PAA blocked Akata cells and in chemically induced Raji cells. Several genes with presumed late functions were found to be expressed with early kinetics and independent of viral DNA replication, suggesting possible novel functions for these genes. Finally, the EBV array was used to identify Rta responsive gene expression in Raji cells, and in the EBV-positive epithelial cells NA, using a Zta siRNA strategy. The array data were confirmed by Northern blotting, RT-PCR and reporter assays. All the information here thus provides a better understanding of the control of EBV lytic gene expression. |
Databáze: | OpenAIRE |
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