Macnaughton Thomas B, Lai Michael M C
Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, California 90033-1054, USA.
J Virol. 2002 Apr;76(8):3928-35. doi: 10.1128/jvi.76.8.3928-3935.2002.
Hepatitis delta virus (HDV) contains a viroid-like circular RNA that replicates via a double rolling circle replication mechanism. It is generally assumed that HDV RNA is synthesized and remains exclusively in the nucleus until being exported to the cytoplasm for virion assembly. Using a [32P]orthophosphate metabolic labeling procedure to study HDV RNA replication (T. B. Macnaughton, S. T. Shi, L. E. Modahl, and M. M. C. Lai. J. Virol. 76:3920-3927, 2002), we unexpectedly found that a significant amount of newly synthesized HDV RNA was detected in the cytoplasm. Surprisingly, Northern blot analysis revealed that the genomic-sense HDV RNA is present almost equally in both the nucleus and cytoplasm, whereas antigenomic HDV RNA was mostly retained in the nucleus, suggesting the specific and highly selective export of genomic HDV RNA. Kinetic studies showed that genomic HDV RNA was exported soon after synthesis. However, only the monomer and, to a lesser extent, the dimer HDV RNAs were exported to the cytoplasm; very little higher-molecular-weight HDV RNA species were detected in the cytoplasm. These results suggest that the cleavage and processing of HDV RNA may facilitate RNA export. The export of genomic HDV RNA was resistant to leptomycin B, indicating that a cell region maintenance 1 (Crm1)-independent pathway was involved. The large form of hepatitis delta antigen (L-HDAg), which is responsible for virus packaging, was not required for RNA export, as a mutant HDV RNA genome unable to synthesize L-HDAg was still exported. The proportions of genomic HDV RNA in the nucleus and cytoplasm remained relatively constant throughout replication, indicating that export of genomic HDV RNA occurred continuously. In contrast, while antigenomic HDV RNA was predominantly in the nucleus, there was a proportionally large fraction of antigenomic HDV RNA in the cytoplasm at early time points of RNA replication. These findings uncover a previously unrecognized presence of HDV RNA in the cytoplasm, which may have implications for viral RNA synthesis and packaging.
丁型肝炎病毒(HDV)含有一种类病毒样环状RNA,其通过双滚环复制机制进行复制。一般认为,HDV RNA在细胞核中合成并一直保留在细胞核内,直到被转运到细胞质中进行病毒体组装。我们使用[32P]正磷酸盐代谢标记法研究HDV RNA复制(T. B. 麦克诺顿、S. T. 施、L. E. 莫达尔和M. M. C. 赖。《病毒学杂志》76:3920 - 3927, 2002),意外地发现在细胞质中检测到大量新合成的HDV RNA。令人惊讶的是,Northern印迹分析显示,基因组意义上的HDV RNA在细胞核和细胞质中的含量几乎相等,而反基因组HDV RNA大多保留在细胞核中,这表明基因组HDV RNA存在特异性且高度选择性的转运。动力学研究表明,基因组HDV RNA在合成后很快就被转运出去。然而,只有单体HDV RNA以及少量二聚体HDV RNA被转运到细胞质中;在细胞质中检测到的高分子量HDV RNA种类极少。这些结果表明,HDV RNA的切割和加工可能有助于RNA的转运。基因组HDV RNA的转运对雷帕霉素B具有抗性,这表明涉及一种不依赖细胞区域维持蛋白1(Crm1)的途径。负责病毒包装的大形式丁型肝炎抗原(L - HDAg)对于RNA的转运并非必需,因为一个无法合成L - HDAg的突变HDV RNA基因组仍能被转运。在整个复制过程中,基因组HDV RNA在细胞核和细胞质中的比例保持相对恒定,这表明基因组HDV RNA的转运是持续发生的。相比之下,虽然反基因组HDV RNA主要存在于细胞核中,但在RNA复制的早期时间点,细胞质中存在比例较大的反基因组HDV RNA。这些发现揭示了HDV RNA在细胞质中以前未被认识到的存在情况,这可能对病毒RNA的合成和包装具有重要意义。