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• W2135705988 endingPage "130119" @default.
• W2135705988 startingPage "130119" @default.
• W2135705988 abstract "Previous studies have reported the detection of a truncated E1 mRNA generated from HPV-18 in HeLa cells. Although it is unclear whether a truncated E1 protein could function as a replicative helicase for viral replication, it would still retain binding sites for potential interactions with different host cell proteins. Furthermore, in this study, we found evidence in support of expression of full-length HPV-18 E1 mRNA in HeLa cells. To determine whether interactions between E1 and cellular proteins play an important role in cellular processes other than viral replication, genome-wide expression profiles of HPV-18 positive HeLa cells were compared before and after the siRNA knockdown of E1 expression. Differential expression and gene set enrichment analysis uncovered four functionally related sets of genes implicated in host defence mechanisms against viral infection. These included the toll-like receptor, interferon and apoptosis pathways, along with the antiviral interferon-stimulated gene set. In addition, we found that the transcriptional coactivator E1A-binding protein p300 (EP300) was downregulated, which is interesting given that EP300 is thought to be required for the transcription of HPV-18 genes in HeLa cells. The observed changes in gene expression produced via the silencing of HPV-18 E1 expression in HeLa cells indicate that in addition to its well-known role in viral replication, the E1 protein may also play an important role in mitigating the host's ability to defend against viral infection." @default.
• W2135705988 created "2016-06-24" @default.
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• W2135705988 date "2014-10-01" @default.
• W2135705988 modified "2023-09-25" @default.
• W2135705988 title "A systems biology analysis of the changes in gene expression via silencing of HPV-18 E1 expression in HeLa cells" @default.
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• W2135705988 doi "https://doi.org/10.1098/rsob.130119" @default.
• W2135705988 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4221889" @default.
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