Suppr超能文献

三基因块编码病毒采用的多样化运动策略。

Varied movement strategies employed by triple gene block-encoding viruses.

机构信息

Oklahoma State University, Department of Entomology and Plant Pathology, Stillwater, OK 74078, USA.

出版信息

Mol Plant Microbe Interact. 2010 Oct;23(10):1231-47. doi: 10.1094/MPMI-04-10-0086.

Abstract

Several RNA virus genera belonging to the Virgaviridae and Flexiviridae families encode proteins organized in a triple gene block (TGB) that facilitate cell-to-cell and long-distance movement. The TGB proteins have been traditionally classified as hordei-like or potex-like based on phylogenetic comparisons and differences in movement mechanisms of the Hordeivirus and Potexvirus spp. However, accumulating data from other model viruses suggests that a revised framework is needed to accommodate the profound differences in protein interactions occurring during infection and ancillary capsid protein requirements for movement. The goal of this article is to highlight common features of the TGB proteins and salient differences in movement properties exhibited by individual viruses encoding these proteins. We discuss common and divergent aspects of the TGB transport machinery, describe putative nucleoprotein movement complexes, highlight recent data on TGB protein interactions and topological properties, and review membrane associations occurring during subcellular targeting and cell-to-cell movement. We conclude that the existing models cannot be used to explain all TGB viruses, and we propose provisional Potexvirus, Hordeivirus, and Pomovirus models. We also suggest areas that might profit from future research on viruses harboring this intriguing arrangement of movement proteins.

摘要

几种属于 Virgaviridae 和 Flexiviridae 科的 RNA 病毒属编码的蛋白质组织在一个三基因块(TGB)中,这有助于细胞间和长距离运动。根据系统发育比较和 Hordeivirus 和 Potexvirus spp. 运动机制的差异,TGB 蛋白传统上被分为类大麦或类 P 病毒。然而,来自其他模式病毒的累积数据表明,需要一个修订的框架来适应感染过程中发生的蛋白质相互作用的深刻差异和运动所需的辅助衣壳蛋白的要求。本文的目的是强调 TGB 蛋白的共同特征以及编码这些蛋白的个别病毒在运动特性上的显著差异。我们讨论了 TGB 运输机制的共同和不同方面,描述了假定的核蛋白运动复合物,强调了关于 TGB 蛋白相互作用和拓扑特性的最新数据,并回顾了亚细胞靶向和细胞间运动过程中发生的膜关联。我们得出结论,现有的模型不能用来解释所有的 TGB 病毒,我们提出了暂定的 P 病毒、Hordeivirus 和 Pomovirus 模型。我们还建议了可能从携带这种有趣运动蛋白排列的病毒的未来研究中受益的领域。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验