Abstract
BackgroundBovine leukemia virus (BLV) is associated with enzootic bovine leukosis and is closely related to human T-cell leukemia virus type I. The Tax protein of BLV is a transcriptional activator of viral replication and a key contributor to oncogenic potential. We previously identified interesting mutant forms of Tax with elevated (TaxD247G) or reduced (TaxS240P) transactivation effects on BLV replication and propagation. However, the effects of these mutations on functions other than transcriptional activation are unknown. In this study, to identify genes that play a role in the cascade of signal events regulated by wild-type and mutant Tax proteins, we used a large-scale host cell gene-profiling approach.ResultsUsing a microarray containing approximately 18,400 human mRNA transcripts, we found several alterations after the expression of Tax proteins in genes involved in many cellular functions such as transcription, signal transduction, cell growth, apoptosis, stress response, and immune response, indicating that Tax protein has multiple biological effects on various cellular environments. We also found that TaxD247G strongly regulated more genes involved in transcription, signal transduction, and cell growth functions, contrary to TaxS240P, which regulated fewer genes. In addition, the expression of genes related to stress response significantly increased in the presence of TaxS240P as compared to wild-type Tax and TaxD247G. By contrast, the largest group of downregulated genes was related to immune response, and the majority of these genes belonged to the interferon family. However, no significant difference in the expression level of downregulated genes was observed among the Tax proteins. Finally, the expression of important cellular factors obtained from the human microarray results were validated at the RNA and protein levels by real-time quantitative reverse transcription-polymerase chain reaction and western blotting, respectively, after transfecting Tax proteins into bovine cells and human HeLa cells.ConclusionA comparative analysis of wild-type and mutant Tax proteins indicates that Tax protein exerts a significant impact on cellular functions as diverse as transcription, signal transduction, cell growth, stress response and immune response. Importantly, our study is the first report that shows the extent to which BLV Tax regulates the innate immune response.
Highlights
Bovine leukemia virus (BLV) is associated with enzootic bovine leukosis and is closely related to human T-cell leukemia virus type I
The Taxresponsive element (TxRE) consists of a cyclic AMP-response element (CRE)-like sequence, and Tax has been suggested to bind indirectly to this element through cellular factors, such as members of the CREB/ activating transcription factor (ATF) family of basic leucine zipper proteins that have been shown to bind to the CRE-like sequence [5,6,7]
Expression of wild-type and mutant tax proteins in HeLa cells To measure alterations in the expression of host cellular genes regulated by wild-type and mutant Tax proteins with elevated (D247G) and reduced (S240P) transactivation activity, we constructed pCAGGS mammalian expression vectors encoding Tax proteins (TaxWT, TaxS240P, and TaxD247G) that were Flag-tagged at their carboxy termini to facilitate the assay, and these vectors were transfected into human cervical HeLa cells
Summary
Bovine leukemia virus (BLV) is associated with enzootic bovine leukosis and is closely related to human T-cell leukemia virus type I. The Tax protein of BLV is a transcriptional activator of viral replication and a key contributor to oncogenic potential. The Tax protein is known to modulate the expression of cellular genes that are related to the regulation of cell growth [8]. The expression of Tax in primary ovine B lymphocytes, which depends on CD154 and interleukin-4, affects B lymphocyte proliferation, cell cycle phase distribution, and survival, leading to cytokine-independent growth [11]. This immortalization process is correlated with increased Bcl-2 protein levels, nuclear NF-κB accumulation, and a series of intracellular pathways that remain to be characterized [12]. To further understand the mechanisms of action, the identification of Tax-associated host cellular factors and pathways is essential
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