Max-von-Pettenkofer Institut, LMU, Feodor-Lynenstr. 25, 81377 Munich, Germany; E-Mails:
Viruses. 2009 Dec;1(3):420-40. doi: 10.3390/v1030420. Epub 2009 Oct 19.
Investigating and assigning gene functions of herpesviruses is a process, which profits from consistent technical innovation. Cloning of bacterial artificial chromosomes encoding herpesvirus genomes permits nearly unlimited possibilities in the construction of genetically modified viruses. Targeted or randomized screening approaches allow rapid identification of essential viral proteins. Nevertheless, mapping of essential genes reveals only limited insight into function. The usage of dominant-negative (DN) proteins has been the tool of choice to dissect functions of proteins during the viral life cycle. DN proteins also facilitate the analysis of host-virus interactions. Finally, DNs serve as starting-point for design of new antiviral strategies.
研究和分配疱疹病毒的基因功能是一个过程,它得益于持续的技术创新。克隆编码疱疹病毒基因组的细菌人工染色体允许在构建遗传修饰病毒方面具有几乎无限的可能性。靶向或随机筛选方法允许快速鉴定病毒的必需蛋白。然而,必需基因的图谱仅能提供对功能的有限了解。显性负(DN)蛋白的使用一直是在病毒生命周期中剖析蛋白功能的首选工具。DN 蛋白还促进了宿主-病毒相互作用的分析。最后,DN 蛋白可作为设计新抗病毒策略的起点。