首页> 美国卫生研究院文献>Journal of Virology >Inactivating a Cellular Intrinsic Immune Defense Mediated by Daxx Is the Mechanism through Which the Human Cytomegalovirus pp71 Protein Stimulates Viral Immediate-Early Gene Expression
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Inactivating a Cellular Intrinsic Immune Defense Mediated by Daxx Is the Mechanism through Which the Human Cytomegalovirus pp71 Protein Stimulates Viral Immediate-Early Gene Expression

机译:灭活由Daxx介导的细胞内在免疫防御是人类巨细胞病毒pp71蛋白刺激病毒即早基因表达的机制。

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摘要

Human cytomegalovirus (HCMV) masterfully evades adaptive and innate immune responses, allowing infection to be maintained and periodically reactivated for the life of the host. Here we show that cells also possess an intrinsic immune defense against HCMV that is disarmed by the virus. In HCMV-infected cells, the promyelocytic leukemia nuclear body (PML-NB) protein Daxx silences viral immediate-early gene expression through the action of a histone deacetylase. However, this antiviral tactic is efficiently neutralized by the viral pp71 protein, which is incorporated into virions, delivered to cells upon infection, and mediates the proteasomal degradation of Daxx. This work demonstrates the mechanism through which pp71 activates viral immediate-early gene expression in HCMV-infected cells. Furthermore, it provides insight into how a PML-NB protein institutes an intrinsic immune defense against a DNA virus and how HCMV pp71 inactivates this defense.
机译:人类巨细胞病毒(HCMV)熟练地逃避了适应性免疫和先天性免疫反应,使感染得以维持并在宿主的生命周期内定期重新激活。在这里,我们显示细胞还具有针对HCMV的固有免疫防御能力,该防御能力被病毒解除了武装。在感染HCMV的细胞中,早幼粒细胞白血病核蛋白(PML-NB)蛋白Daxx通过组蛋白脱乙酰基酶的作用使病毒即刻早期基因表达沉默。然而,这种抗病毒策略被病毒pp71蛋白有效地中和,该病毒被掺入病毒粒子,在感染后被递送至细胞,并介导Daxx的蛋白酶体降解。这项工作证明了pp71激活HCMV感染细胞中病毒即刻早期基因表达的机制。此外,它提供了有关PML-NB蛋白如何建立针对DNA病毒的内在免疫防御以及HCMV pp71如何激活这种防御的见解。

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