D'Souza Victoria, Summers Michael F
Howard Hughes Medical Institute and Department of Chemistry and Biochemistry, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, USA.
Nat Rev Microbiol. 2005 Aug;3(8):643-55. doi: 10.1038/nrmicro1210.
As retroviruses assemble in infected cells, two copies of their full-length, unspliced RNA genomes are selected for packaging from a cellular milieu that contains a substantial excess of non-viral and spliced viral RNAs. Understanding the molecular details of genome packaging is important for the development of new antiviral strategies and to enhance the efficacy of retroviral vectors used in human gene therapy. Recent studies of viral RNA structure in vitro and in vivo and high-resolution studies of RNA fragments and protein-RNA complexes are helping to unravel the mechanism of genome packaging and providing the first glimpses of the initial stages of retrovirus assembly.
逆转录病毒在受感染细胞中组装时,会从细胞环境中挑选出两份全长、未剪接的RNA基因组进行包装,而该细胞环境中含有大量过量的非病毒RNA和剪接后的病毒RNA。了解基因组包装的分子细节对于开发新的抗病毒策略以及提高用于人类基因治疗的逆转录病毒载体的功效至关重要。最近在体外和体内对病毒RNA结构的研究以及对RNA片段和蛋白质-RNA复合物的高分辨率研究,有助于揭示基因组包装的机制,并首次让我们了解到逆转录病毒组装的初始阶段。