Ohshima K, Shiroki K
J Virol. 1986 Feb;57(2):490-6. doi: 10.1128/JVI.57.2.490-496.1986.
An adenovirus type 12 mutant, in203S, was constructed to contain an insertion of two amino acids in the early region 1A (E1A) 13S mRNA-coding region and in the E1A 12S mRNA intron. in203S could not grow in HeLa and KB cells. Virus DNA replication was scarcely detected at a low multiplicity of infection, but was detected at a high multiplicity of infection. The transcription of early genes other than E1A was not detected at 13 h after infection, but became detectable after longer incubation. The transcription of the E1A gene was also reduced to about one-fifth of the wild-type level. The mutant induced fewer foci of smaller sizes than the wild type in rat 3Y1 and secondary rat kidney cells. The induction of cellular DNA synthesis was reduced in rat 3Y1 cells infected with in203S as compared with that in wild type-infected cells. These results show that the E1A 13S mRNA-derived polypeptide of adenovirus type 12 is required for activation of early genes, cell transformation, and induction of cellular DNA synthesis.
构建了一种12型腺病毒突变体in203S,使其在早期区域1A(E1A)13S mRNA编码区和E1A 12S mRNA内含子中插入两个氨基酸。in203S不能在HeLa和KB细胞中生长。在低感染复数时几乎检测不到病毒DNA复制,但在高感染复数时可以检测到。感染后13小时未检测到除E1A外的早期基因转录,但长时间培养后可检测到。E1A基因的转录也降至野生型水平的约五分之一。与野生型相比,该突变体在大鼠3Y1和二代大鼠肾细胞中诱导的病灶数量更少、尺寸更小。与野生型感染的细胞相比,感染in203S的大鼠3Y1细胞中细胞DNA合成的诱导减少。这些结果表明,12型腺病毒的E1A 13S mRNA衍生多肽是早期基因激活、细胞转化和细胞DNA合成诱导所必需的。