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The latency-related gene of bovine herpesvirus 1 encodes a product which inhibits cell cycle progression

机译:牛疱疹病毒1的潜伏相关基因编码抑制细胞周期进程的产物

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摘要

Bovine herpesvirus 1 (BHV-1) establishes a latent infection in the sensory ganglionic neurons of cattle. The exclusive viral RNA expressed in a latent infection is the latency-related (LR) RNA, suggesting that it regulates some aspect of a latent infection. During the course of a productive infection, alphaherpesviruses induce certain events which occur during cell cycle progression. Consequently, we hypothesized that a BHV-1 infection might induce events in neurons which occur during cell cycle progression. In agreement with this hypothesis, cyclin A was detected in neurons of trigeminal ganglia when rabbits were infected. Neuronal cell cycle progression or inappropriate expression of cyclin A leads to apoptosis, suggesting that a viral factor inhibits the deleterious effects of cyclin A expression. The BHV-1 LR gene inhibited cell cycle progression and proliferation of human osteosarcoma cells. Antibodies directed against cyclin A or the LR protein coprecipitated the LR protein or cyclin A, respectively, suggesting that the two proteins interact with each other. We conclude that LR gene products inhibit cell cycle progression and hypothesize that this activity enhances the survival of infected neurons.
机译:牛Herpesvirus 1(Bhv-1)在牛的感觉神经节神经元中建立了潜在感染。在潜在感染中表达的独占病毒RNA是潜伏期(LR)RNA,表明它调节潜在感染的某些方面。在生产感染过程中,Alphaherpesviruses诱导细胞周期进展期间发生的某些事件。因此,我们假设BHV-1感染可能会诱导在细胞周期进展期间发生的神经元中的事件。同意这种假设,当兔子被感染时,在三叉甘氨酸的神经元中检测到细胞周期蛋白A.神经元细胞周期的进展或细胞周期蛋白A的不当表达导致细胞凋亡,表明病毒因素抑制了细胞周期蛋白表达的有害影响。 BHV-1 LR基因抑制了人骨瘤细胞的细胞周期进展和增殖。针对细胞周期蛋白A或LR蛋白的抗体分别共培养了LR蛋白或细胞周期蛋白A,表明两种蛋白质彼此相互作用。我们得出结论,LR基因产品抑制细胞周期进展,并假设该活性增强感染神经元的存活率。

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