Zhang W, Low J A, Christensen J B, Imperiale M 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. 2001 Nov;75(21):10446-54. doi: 10.1128/JVI.75.21.10446-10454.2001.
Although it has been demonstrated that the adenovirus IVa2 protein binds to the packaging domains on the viral chromosome and interacts with the viral L1 52/55-kDa protein, which is required for viral DNA packaging, there has been no direct evidence demonstrating that the IVa2 protein is involved in DNA packaging. To understand in greater detail the DNA packaging mechanisms of adenovirus, we have asked whether DNA packaging is serotype or subgroup specific. We found that Ad7 (subgroup B), Ad12 (subgroup A), and Ad17 (subgroup D) cannot complement the defect of an Ad5 (subgroup C) mutant, pm8001, which does not package its DNA due to a mutation in the L1 52/55-kDa gene. This indicates that the DNA packaging systems of different serotypes cannot interact productively with Ad5 DNA. Based on this, a chimeric virus containing the Ad7 genome except for the inverted terminal repeats and packaging sequence from Ad5 was constructed. This chimeric virus replicates its DNA and synthesizes Ad7 proteins, but it cannot package its DNA in 293 cells or 293 cells expressing the Ad5 L1 52/55-kDa protein. However, this chimeric virus packages its DNA in 293 cells expressing the Ad5 IVa2 protein. These results indicate that the IVa2 protein plays a role in viral DNA packaging and that its function is serotype specific. Since this chimeric virus cannot package its own DNA, but produces all the components for packaging Ad7 DNA, it may be a more suitable helper virus for the growth of Ad7 gutted vectors for gene transfer.
尽管已经证明腺病毒IVa2蛋白可与病毒染色体上的包装结构域结合,并与病毒DNA包装所需的病毒L1 52/55-kDa蛋白相互作用,但尚无直接证据表明IVa2蛋白参与DNA包装。为了更详细地了解腺病毒的DNA包装机制,我们探讨了DNA包装是否具有血清型或亚组特异性。我们发现Ad7(B亚组)、Ad12(A亚组)和Ad17(D亚组)不能弥补Ad5(C亚组)突变体pm8001的缺陷,该突变体由于L1 52/55-kDa基因的突变而无法包装其DNA。这表明不同血清型的DNA包装系统不能与Ad5 DNA有效相互作用。基于此,构建了一种嵌合病毒,其除了来自Ad5的反向末端重复序列和包装序列外,包含Ad7基因组。这种嵌合病毒复制其DNA并合成Ad7蛋白,但它不能在293细胞或表达Ad5 L1 52/55-kDa蛋白的293细胞中包装其DNA。然而,这种嵌合病毒在表达Ad5 IVa2蛋白的293细胞中包装其DNA。这些结果表明IVa2蛋白在病毒DNA包装中起作用,并且其功能具有血清型特异性。由于这种嵌合病毒不能包装其自身的DNA,但产生用于包装Ad7 DNA的所有成分,它可能是用于基因转移的Ad7缺失载体生长的更合适的辅助病毒。