Daniels Robert, Sadowicz Dorota, Hebert Daniel N
Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, Massachusetts, United States of America.
PLoS Pathog. 2007 Jul;3(7):e98. doi: 10.1371/journal.ppat.0030098.
How nonenveloped viruses such as simian virus 40 (SV40) trigger the lytic release of their progeny is poorly understood. Here, we demonstrate that SV40 expresses a novel later protein termed VP4 that triggers the timely lytic release of its progeny. Like VP3, VP4 synthesis initiates from a downstream AUG start codon within the VP2 transcript and localizes to the nucleus. However, VP4 expression occurs approximately 24 h later at a time that coincides with cell lysis, and it is not incorporated into mature virions. Mutation of the VP4 initiation codon from the SV40 genome delayed lysis by 2 d and reduced infectious particle release. Furthermore, the co-expression of VP4 and VP3, but not their individual expression, recapitulated cell lysis in bacteria. Thus, SV40 regulates its life cycle by the later temporal expression of VP4, which results in cell lysis and enables the 50-nm virus to exit the cell. This study also demonstrates how viruses can generate multiple proteins with diverse functions and localizations from a single reading frame.
像猴病毒40(SV40)这样的无包膜病毒如何触发其后代的裂解释放,目前还知之甚少。在这里,我们证明SV40表达一种名为VP4的新型晚期蛋白,它能触发其后代的适时裂解释放。与VP3一样,VP4的合成起始于VP2转录本内下游的AUG起始密码子,并定位于细胞核。然而,VP4的表达大约在24小时后发生,此时与细胞裂解时间一致,并且它不会被整合到成熟病毒颗粒中。SV40基因组中VP4起始密码子的突变使裂解延迟了2天,并减少了感染性颗粒的释放。此外,VP4和VP3的共表达,而不是它们的单独表达,在细菌中重现了细胞裂解。因此,SV40通过VP4的晚期瞬时表达来调节其生命周期,这导致细胞裂解,并使50纳米的病毒能够离开细胞。这项研究还展示了病毒如何从单个阅读框产生具有不同功能和定位的多种蛋白质。