Cullen Bryan R
Howard Hughes Medical Institute and Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Trends Biochem Sci. 2003 Aug;28(8):419-24. doi: 10.1016/S0968-0004(03)00142-7.
To maximize the production of progeny virions, several viruses have evolved mechanisms that promote the selective nuclear export of viral mRNA transcripts while, in some cases, inhibiting the export of cellular mRNAs. To achieve this goal, viruses have evolved regulatory proteins and cis-acting RNA elements that selectively interact with key cellular nuclear export factors. Efforts to identify the cellular targets of these viral proteins and RNA elements have led to the identification of Crm1 and Tap as essential human nuclear RNA-export factors and continue to provide insights into how mRNAs are selected for export
为了使子代病毒粒子的产量最大化,几种病毒已经进化出促进病毒mRNA转录本选择性核输出的机制,在某些情况下,还会抑制细胞mRNA的输出。为实现这一目标,病毒进化出了调控蛋白和顺式作用RNA元件,它们能与关键的细胞内核输出因子选择性相互作用。识别这些病毒蛋白和RNA元件细胞靶点的研究工作,已使Crm1和Tap被鉴定为重要的人类细胞核RNA输出因子,并不断为mRNA如何被选择用于输出提供见解。