Bridge E, Medghalchi S, Ubol S, Leesong M, Ketner G
Department of Immunology and Infectious Diseases, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland 21205.
Virology. 1993 Apr;193(2):794-801. doi: 10.1006/viro.1993.1188.
Mutants of human adenovirus type 5 (Ad5) lacking early region 4 (E4) display a complex phenotype that includes a delay in the onset of viral DNA replication in low-multiplicity infections. Studies of viral DNA replication in vitro have not revealed a requirement for E4 products in DNA synthesis and, for most E4 mutants, defects in DNA replication are not apparent at high multiplicities of infection. The effects of E4 mutations on DNA replication therefore may reflect a role for E4 in the regulation of replication rather than in the process of DNA synthesis. The E4 mutant H5d/1014 carries two deletion mutations that together destroy all E4 open reading frames (ORFs) except ORF 4. Immunoprecipitation measurements of the level of the ORF 4 product confirm that H5d/1014 accumulates the ORF 4 product in somewhat larger amounts than wild-type Ad5. H5d/1014 is profoundly defective in viral DNA replication at a multiplicity of infection (50 PFU/cell) and time (24 hr after infection) that permit mutants lacking all seven E4 products to accumulate approximately normal amounts of DNA. In contrast, H5d/1019, a derivative of H5d/1014 in which the expression of ORF 4 is prevented by a mutation in the ORF 4 ATG initiator codon, produces DNA normally under these conditions. The product of ORF 4 therefore is necessary for the inhibition of viral DNA replication in H5d/1014-infected cells. H5d/1014 also inhibits, in trans, the synthesis of viral DNA by other E4 mutants that lack both E4 ORFs 3 and 6. Viruses that possess either of those ORFs are not subject to inhibition, indicating that the ORF3 and 6 products antagonize the effect of ORF 4. These observations are consistent with a regulatory role for the E4 ORF 3, 4, and 6 products in viral DNA replication in adenovirus-infected cells.
缺乏早期区域4(E4)的人5型腺病毒(Ad5)突变体表现出复杂的表型,包括在低 multiplicity 感染中病毒DNA复制起始延迟。体外病毒DNA复制研究未揭示DNA合成中对E4产物的需求,并且对于大多数E4突变体,在高 multiplicity 感染时DNA复制缺陷并不明显。因此,E4突变对DNA复制的影响可能反映了E4在复制调控中的作用,而非在DNA合成过程中的作用。E4突变体H5d/1014携带两个缺失突变,共同破坏了除ORF 4外的所有E4开放阅读框(ORF)。对ORF 4产物水平的免疫沉淀测量证实,H5d/1014积累的ORF 4产物量比野生型Ad5略多。在允许缺乏所有七种E4产物的突变体积累大致正常量DNA的感染 multiplicity(50 PFU/细胞)和时间(感染后24小时)下,H5d/1014在病毒DNA复制方面存在严重缺陷。相比之下,H5d/1019是H5d/1014的衍生物,其中ORF 4的表达因ORF 4 ATG起始密码子的突变而被阻止,在这些条件下能正常产生DNA。因此,ORF 4产物对于抑制H5d/1014感染细胞中的病毒DNA复制是必需的。H5d/1014还能反式抑制其他同时缺乏E4 ORF 3和6的E4突变体的病毒DNA合成。拥有这两个ORF中任何一个的病毒不受抑制,表明ORF3和6产物拮抗ORF 4的作用。这些观察结果与E4 ORF