首页> 美国卫生研究院文献>Viruses >Identification of Marek’s Disease Virus VP22 Tegument Protein Domains Essential for Virus Cell-to-Cell Spread Nuclear Localization Histone Association and Cell-Cycle Arrest
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Identification of Marek’s Disease Virus VP22 Tegument Protein Domains Essential for Virus Cell-to-Cell Spread Nuclear Localization Histone Association and Cell-Cycle Arrest

机译:识别马立克氏病病毒VP22皮膜蛋白质结构域这些结构域对病毒的细胞间传播核定位组蛋白缔合和细胞周期逮捕至关重要

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摘要

VP22 is a major tegument protein of alphaherpesviruses encoded by the UL49 gene. Two properties of VP22 were discovered by studying Marek’s disease virus (MDV), the Mardivirus prototype; it has a major role in virus cell-to-cell spread and in cell cycle modulation. This 249 AA-long protein contains three regions including a conserved central domain. To decipher the functional VP22 domains and their relationships, we generated three series of recombinant MDV genomes harboring a modified UL49 gene and assessed their effect on virus spread. Mutated VP22 were also tested for their ability to arrest the cell cycle, subcellular location and histones copurification after overexpression in cells. We demonstrated that the N-terminus of VP22 associated with its central domain is essential for virus spread and cell cycle modulation. Strikingly, we demonstrated that AAs 174-190 of MDV VP22 containing the end of a putative extended alpha-3 helix are essential for both functions and that AAs 159–162 located in the putative beta-strand of the central domain are mandatory for cell cycle modulation. Despite being non-essential, the 59 C-terminal AAs play a role in virus spread efficiency. Interestingly, a positive correlation was observed between cell cycle modulation and VP22 histones association, but none with MDV spread.
机译:VP22是由UL49基因编码的α疱疹病毒的主要外被蛋白。通过研究Marek病毒原型Marek病病毒(MDV),发现了VP22的两个特性。它在病毒细胞间传播和细胞周期调控中起主要作用。该249个AA长的蛋白质包含三个区域,包括保守的中央结构域。为了破译功能性VP22域及其相互关系,我们生成了三个包含修饰的UL49基因的重组MDV基因组,并评估了它们对病毒传播的影响。还测试了突变的VP22在细胞中过度表达后能够阻止细胞周期,亚细胞定位和组蛋白共纯化的能力。我们证明,VP22的N末端与其中央结构域相关,对于病毒传播和细胞周期调控至关重要。令人惊讶地,我们证明了MDV VP22的AA 174-190包含推定的扩展alpha-3螺旋末端对于这两种功能都是必不可少的,并且位于中央域推定的β链中的AA 159-162对于细胞周期是必不可少的调制。尽管不是必需的,但59个C末端AA仍在病毒传播效率中起作用。有趣的是,在细胞周期调节和VP22组蛋白缔合之间观察到正相关,但没有与MDV扩散相关。

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