Zhang Wei, Imperiale Michael J
Department of Microbiology and Immunology, Center for Gene Therapy and Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan 48109-0942, USA.
J Virol. 2003 Mar;77(6):3586-94. doi: 10.1128/jvi.77.6.3586-3594.2003.
The adenovirus L1 52/55-kDa protein is required for viral DNA packaging and interacts with the viral IVa2 protein, which binds to the viral packaging sequence. Previous reports suggest that the IVa2 protein plays a role in viral DNA packaging and that this function of the IVa2 protein is serotype specific. To further examine the function of the IVa2 protein in viral DNA packaging, a mutant virus that does not express the IVa2 protein was constructed by introducing two stop codons at the beginning of the IVa2 open reading frame in a full-length bacterial clone of adenovirus type 5. The mutant virus, pm8002, was defective for growth in 293 cells, although it replicated its DNA and produced early and late viral proteins. Electron microscopic and gradient analyses revealed that the mutant virus did not assemble any viral particles in 293 cells. In 293-IVa2 cells, which express the IVa2 protein, infectious viruses were produced, although the titer of the mutant virus was lower than that of the wild-type virus, indicating that these cells may not fully complement the mutation. The mutant viral particles produced in 293-IVa2 cells were heterogeneous in size and shape, less stable, and did not traffic efficiently to the nucleus. Marker rescue experiments with a wild-type IVa2 DNA fragment confirmed that the only mutations present in pm8002 were in the IVa2 gene. The results indicate that the IVa2 protein is required for adenovirus assembly and suggest that virus particles may be assembled around the DNA rather than DNA being packaged into preformed capsids.
腺病毒L1 52/55-kDa蛋白是病毒DNA包装所必需的,并且与病毒IVa2蛋白相互作用,后者结合病毒包装序列。先前的报道表明,IVa2蛋白在病毒DNA包装中起作用,并且IVa2蛋白的这一功能具有血清型特异性。为了进一步研究IVa2蛋白在病毒DNA包装中的功能,通过在腺病毒5型全长细菌克隆的IVa2开放阅读框起始处引入两个终止密码子,构建了一种不表达IVa2蛋白的突变病毒。突变病毒pm8002在293细胞中生长存在缺陷,尽管它能复制其DNA并产生早期和晚期病毒蛋白。电子显微镜和梯度分析显示,该突变病毒在293细胞中未组装任何病毒颗粒。在表达IVa2蛋白的293-IVa2细胞中产生了感染性病毒,尽管突变病毒的滴度低于野生型病毒,这表明这些细胞可能不能完全补偿该突变。在293-IVa2细胞中产生的突变病毒颗粒在大小和形状上是异质的,稳定性较差,并且不能有效地转运到细胞核。用野生型IVa2 DNA片段进行的标记拯救实验证实,pm8002中存在的唯一突变位于IVa2基因。结果表明,IVa2蛋白是腺病毒组装所必需的,并提示病毒颗粒可能围绕DNA组装,而不是DNA被包装到预先形成的衣壳中。