Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, United States.
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Elife. 2021 Feb 8;10:e62261. doi: 10.7554/eLife.62261.
Genome packaging in large double-stranded DNA viruses requires a powerful molecular motor to force the viral genome into nascent capsids, which involves essential accessory factors that are poorly understood. Here, we present structures of two such accessory factors from the oncogenic herpesviruses Kaposi's sarcoma-associated herpesvirus (KSHV; ORF68) and Epstein-Barr virus (EBV; BFLF1). These homologous proteins form highly similar homopentameric rings with a positively charged central channel that binds double-stranded DNA. Mutation of individual positively charged residues within but not outside the channel ablates DNA binding, and in the context of KSHV infection, these mutants fail to package the viral genome or produce progeny virions. Thus, we propose a model in which ORF68 facilitates the transfer of newly replicated viral genomes to the packaging motor.
大型双链 DNA 病毒的基因组包装需要一种强大的分子马达将病毒基因组强行压入新生衣壳中,这涉及到尚未完全了解的基本辅助因子。在这里,我们展示了两种致癌疱疹病毒(卡波西肉瘤相关疱疹病毒(KSHV;ORF68)和 Epstein-Barr 病毒(EBV;BFLF1)中的此类辅助因子的结构。这些同源蛋白形成高度相似的五聚体环,带有带正电荷的中央通道,可结合双链 DNA。通道内而非通道外的单个带正电荷残基的突变会破坏 DNA 结合,在 KSHV 感染的情况下,这些突变体无法包装病毒基因组或产生子代病毒颗粒。因此,我们提出了一个模型,其中 ORF68 有助于将新复制的病毒基因组转移到包装马达上。