Odawara T, Oshima M, Doi K, Iwamoto A, Yoshikura H
Department of Bacteriology, Faculty of Medicine, University of Tokyo, Bunkyo-ku, Tokyo 113, Japan.
J Virol. 1998 Jul;72(7):5414-24. doi: 10.1128/JVI.72.7.5414-5424.1998.
The gag-pol readthrough mutant of Moloney murine leukemia virus, MLV-B(CAG) (T. Odawara, H. Yoshikura, M. Oshima, T. Tanaka, D. S. Jones, F. Nemoto, Y. Kuchino, and A. Iwamoto, J. Virol. 65:6376-6379, 1991), was poorly complemented by a mutant encoding only Gag. This is because with all the genetic elements necessary for env expression present in MLV-B(CAG), insufficient Env protein was produced by the cells expressing MLV-B(CAG) for efficient virus production. Since the env mRNA expression per provirus in the MLV-B(CAG)- and wild-type-MLV-producing cells were the same and since the cells expressing the former contained eightfold fewer proviral copies, the insufficient Env expression by the former was found to be due to insufficient proviral copies in the cells. Examination of the cell clones having various proviral copies of Deltawt MLV (M. Oshima, T. Odawara, T. Matano, H. Sakahira, Y. Kuchino, A. Iwamoto, and H. Yoshikura, J. Virol. 70:2286-2295, 1996) showed that mRNA level was proportional to the number of proviral copies while interference and virus production followed a sigmoid curve with a sharp rise at the threshold number of proviral copies of around four per cell. Multicycle infection probably continues until the threshold level of proviral copies is attained in natural infection too.
莫洛尼鼠白血病病毒的gag-pol通读突变体MLV-B(CAG)(T. 小田原、H. 吉仓、M. 大岛、T. 田中、D. S. 琼斯、F. 根本、Y. 久智野、A. 岩本,《病毒学杂志》65:6376 - 6379, 1991),仅编码Gag的突变体对其互补性较差。这是因为在MLV-B(CAG)中存在env表达所需的所有遗传元件,但表达MLV-B(CAG)的细胞产生的Env蛋白不足以高效产生病毒。由于在产生MLV-B(CAG)的细胞和野生型MLV的细胞中,每个前病毒的env mRNA表达相同,且表达前者的细胞中的前病毒拷贝数少八倍,因此发现前者Env表达不足是由于细胞中的前病毒拷贝数不足。对具有不同前病毒拷贝数的Deltawt MLV细胞克隆的研究(M. 大岛、T. 小田原、T. 真野、H. 坂平、Y. 久智野、A. 岩本、H. 吉仓,《病毒学杂志》70:2286 - 2295, 1996)表明,mRNA水平与前病毒拷贝数成正比,而干扰和病毒产生则呈S形曲线,在每个细胞约四个前病毒拷贝的阈值数量处急剧上升。在自然感染中,多轮感染可能也会持续到达到前病毒拷贝数的阈值水平。