Tanapoxvirus 142R蛋白是一种丝氨酸-苏氨酸激酶,可磷酸化肿瘤抑制因子p53。

The Open Virology Journal Pub Date : 2013-01-01 Epub Date: 2013-01-21 DOI:10.2174/1874357901307010001
Krystal N Seibert, Karim Essani, Bruce E Bejcek
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引用次数: 0

摘要

为了有效地应对病毒感染,哺乳动物依赖于先天和适应性免疫系统。此外,宿主细胞反应,如凋亡在宿主防御机制中也起着至关重要的作用。为了在体内实现成功的复制策略,动物病毒已经进化出多种干扰宿主反应的分子机制。特别是痘病毒,是动物病毒编码多种蛋白质的一个主要例子,这些蛋白质是复制和破坏宿主免疫和单细胞反应所必需的。在牛痘病毒(VV)中已经发现了几种抑制宿主免疫调节细胞因子和感染细胞凋亡的蛋白。在这里,我们描述了一种由天花病毒基因组(142R开放阅读框)编码的蛋白的鉴定,该蛋白与VV的B1R蛋白同源。我们证明,像B1R一样,TPV142R编码一种丝氨酸苏氨酸激酶,该激酶可以使肿瘤抑制因子p53磷酸化,因此具有抑制感染细胞凋亡的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Tanapoxvirus 142R Protein is a Serine-Threonine Kinase that Phosphorylates the Tumor Suppressor p53.

The Tanapoxvirus 142R Protein is a Serine-Threonine Kinase that Phosphorylates the Tumor Suppressor p53.

The Tanapoxvirus 142R Protein is a Serine-Threonine Kinase that Phosphorylates the Tumor Suppressor p53.

The Tanapoxvirus 142R Protein is a Serine-Threonine Kinase that Phosphorylates the Tumor Suppressor p53.

To effectively respond to viral infections, mammals rely on the innate and adaptive immune systems. Additionally, host cellular responses, such as apoptosis also play a vital role in the host defense mechanisms. To accomplish a successful replicative strategy in vivo, animal viruses have evolved a variety of molecular mechanisms that interfere with host responses. Poxviruses in particular, represents a prime example of where animal viruses encode a wide variety of proteins necessary for replication and subversion of the host's immune and single cell responses. Several proteins that inhibit host immmunomodulatory cytokines and apoptosis of infected cells have been characterized in vaccinia virus (VV). Here, we describe the identification of a protein encoded by the tanapox virus genome (142R open reading frame) that is orthologous to the B1R protein from VV. We demonstrate that like B1R, TPV142R encodes a serine threonine kinase that can phosphorylate the tumor suppressor p53 and therefore has the potential for inhibiting apoptosis of infected cells.

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