Departments of 1Laboratory Medicine and.
Genetics, Yale University Medical School, New Haven, Connecticut 06510; email:
Annu Rev Virol. 2014 Nov;1(1):517-37. doi: 10.1146/annurev-virology-031413-085444. Epub 2014 Jul 9.
Parvoviruses are small, rugged, nonenveloped protein particles containing a linear, nonpermuted, single-stranded DNA genome of ∼5 kb. Their limited coding potential requires optimal adaptation to the environment of particular host cells, where entry is mediated by a variable program of capsid dynamics, ultimately leading to genome ejection from intact particles within the host nucleus. Genomes are amplified by a continuous unidirectional strand-displacement mechanism, a linear adaptation of rolling circle replication that relies on the repeated folding and unfolding of small hairpin telomeres to reorient the advancing fork. Progeny genomes are propelled by the viral helicase into the preformed capsid via a pore at one of its icosahedral fivefold axes. Here we explore how the fine-tuning of this unique replication system and the mechanics that regulate opening and closing of the capsid fivefold portals have evolved in different viral lineages to create a remarkably complex spectrum of phenotypes.
细小病毒是小型、坚固、无包膜的蛋白颗粒,含有约 5kb 的线性、未重排、单链 DNA 基因组。它们有限的编码能力需要与特定宿主细胞的环境进行最佳适配,进入宿主细胞是通过衣壳动力学的可变程序介导的,最终导致基因组从完整的衣壳粒子中被逐出到宿主核内。基因组通过连续的单向链置换机制进行扩增,这是一种线性的滚环复制适应,依赖于小发夹端粒的反复折叠和展开,以重新定向前进的叉。通过病毒解旋酶,子代基因组通过其二十面体五重轴之一的一个孔被推进到预先形成的衣壳中。在这里,我们探讨了这种独特的复制系统的微调以及调节衣壳五重门打开和关闭的机制是如何在不同的病毒谱系中进化的,以创造出一个非常复杂的表型谱。