Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
PLoS Pathog. 2010 Jan 29;6(1):e1000741. doi: 10.1371/journal.ppat.1000741.
Virtually all DNA viruses including hepatitis B viruses (HBV) replicate their genome inside the nucleus. In non-dividing cells, the genome has to pass through the nuclear pore complexes (NPCs) by the aid of nuclear transport receptors as e.g. importin beta (karyopherin). Most viruses release their genome in the cytoplasm or at the cytosolic face of the NPC, as the diameter of their capsids exceeds the size of the NPC. The DNA genome of HBV is derived from reverse transcription of an RNA pregenome. Genome maturation occurs in cytosolic capsids and progeny capsids can deliver the genome into the nucleus causing nuclear genome amplification. The karyophilic capsids are small enough to pass the NPC, but nuclear entry of capsids with an immature genome is halted in the nuclear basket on the nuclear side of the NPC, and the genome remains encapsidated. In contrast, capsids with a mature genome enter the basket and consequently liberate the genome. Investigating the difference between immature and mature capsids, we found that mature capsids had to disintegrate in order to leave the nuclear basket. The arrest of a karyophilic cargo at the nuclear pore is a rare phenomenon, which has been described for only very few cellular proteins participating in nuclear entry. We analyzed the interactions causing HBV capsid retention. By pull-down assays and partial siRNA depletion, we showed that HBV capsids directly interact with nucleoporin 153 (Nup153), an essential protein of the nuclear basket which participates in nuclear transport via importin beta. The binding sites of importin beta and capsids were shown to overlap but capsid binding was 150-fold stronger. In cellulo experiments using digitonin-permeabilized cells confirmed the interference between capsid binding and nuclear import by importin beta. Collectively, our findings describe a unique nuclear import strategy not only for viruses but for all karyophilic cargos.
几乎所有的 DNA 病毒,包括乙型肝炎病毒 (HBV),都在内核中复制其基因组。在非分裂细胞中,基因组必须借助核转运受体(如输入蛋白β)穿过核孔复合体 (NPC)。由于其衣壳的直径超过 NPC 的大小,大多数病毒会在细胞质或 NPC 的胞质面释放其基因组。HBV 的 DNA 基因组源自 RNA 前基因组的逆转录。基因组成熟发生在胞质衣壳中,并且子代衣壳可以将基因组递送至核内,导致核基因组扩增。亲核衣壳足够小,可以穿过 NPC,但未成熟基因组的衣壳进入核内被 NPC 核侧的核篮所阻止,并且基因组保持被包裹。相比之下,具有成熟基因组的衣壳进入核篮,从而释放基因组。研究不成熟和成熟衣壳之间的差异时,我们发现成熟衣壳必须解体才能离开核篮。亲核货物在核孔处的滞留是一种罕见的现象,仅在少数参与核进入的细胞蛋白中有所描述。我们分析了导致 HBV 衣壳保留的相互作用。通过下拉测定和部分 siRNA 耗竭,我们表明 HBV 衣壳直接与核孔蛋白 153(Nup153)相互作用,Nup153 是核篮的必需蛋白,通过输入蛋白β参与核转运。证明了输入蛋白β和衣壳的结合位点重叠,但衣壳的结合强度强 150 倍。在使用非离子去污剂通透细胞的细胞内实验中,证实了衣壳结合和输入蛋白β介导的核内输入之间的干扰。总的来说,我们的发现描述了一种独特的核内输入策略,不仅适用于病毒,也适用于所有亲核货物。