Hiscox J A
School of Animal and Microbial Sciences, University of Reading, UK.
Arch Virol. 2002 Jun;147(6):1077-89. doi: 10.1007/s00705-001-0792-0.
A number of viruses and viral proteins interact with a dynamic sub-nuclear structure called the nucleolus. The nucleolus is present during interphase in mammalian cells and is the site of ribosome biogenesis, and has been implicated in controlling regulatory processes such as the cell cycle. Viruses interact with the nucleolus and its antigens; viral proteins co-localise with factors such as nucleolin, B23 and fibrillarin, and can cause their redistribution during infection. Viruses can use these components as part of their replication process, and also use the nucleolus as a site of replication itself. Many of these properties are not restricted to any particular type of virus or replication mechanism, and examples of these processes can be found in DNA, RNA and retroviruses. Evidence suggests that viruses may target the nucleolus and its components to favour viral transcription, translation and perhaps alter the cell cycle in order to promote virus replication. Autoimmunity to nucleolin and fibrillarin have been associated with a number of diseases, and by targeting the nucleolus and displacing nucleolar antigens, virus infection might play a role in the initiation of these conditions.
许多病毒和病毒蛋白与一种名为核仁的动态亚核结构相互作用。核仁在哺乳动物细胞的间期存在,是核糖体生物合成的场所,并且与控制细胞周期等调节过程有关。病毒与核仁及其抗原相互作用;病毒蛋白与核仁素、B23和纤维蛋白原等因子共定位,并可在感染期间导致它们重新分布。病毒可将这些成分用作其复制过程的一部分,还将核仁本身作为复制位点。许多这些特性并不局限于任何特定类型的病毒或复制机制,在DNA病毒、RNA病毒和逆转录病毒中都能找到这些过程的例子。有证据表明,病毒可能靶向核仁及其成分,以促进病毒转录、翻译,并可能改变细胞周期以促进病毒复制。针对核仁素和纤维蛋白原的自身免疫与多种疾病有关,通过靶向核仁并取代核仁抗原,病毒感染可能在这些疾病的引发中起作用。