Longiaru M, Horwitz M S
Department of Microbiology-Immunology, Albert Einstein College of Medicine, Bronx, New York 10461.
Mol Cell Biol. 1981 Mar;1(3):208-15. doi: 10.1128/mcb.1.3.208-215.1981.
Chinese hamster ovary (CHO) cells infected with adenovirus type 2 (Ad2) produced amounts of viral deoxyribonucleic acid (DNA) equal to that synthesized in permissively infected HeLa cells. However, there was 6,000-fold less virion produced in CHO cells. Since the structural viral polypeptides were not detected by pulse-labeling CHO cells at various times postinfection, the block in virion formation is located between the synthesis of viral DNA and late proteins. Extracts of CHO cells could also function in a recently reported in vitro Ad2 DNA synthesis system which is dependent upon the addition of exogenous Ad2 DNA covalently linked to a 5'-terminal protein (Ikeda et al., Proc. Natl. Acad. Sci. U.S.A. 77:5827-5831, 1980). Extracts of infected CHO cytoplasm were able to complement uninfected CHO nuclear extracts to synthesize viral DNA on Ad2 templates. This in vitro replication system has the potential to probe host DNA synthesis requirements as well as viral factors.
感染2型腺病毒(Ad2)的中国仓鼠卵巢(CHO)细胞产生的病毒脱氧核糖核酸(DNA)量与在允许感染的HeLa细胞中合成的量相当。然而,CHO细胞中产生的病毒粒子减少了6000倍。由于在感染后不同时间对CHO细胞进行脉冲标记未检测到病毒结构多肽,因此病毒粒子形成的阻断位于病毒DNA合成和晚期蛋白质合成之间。CHO细胞提取物也可以在最近报道的依赖于添加与5'-末端蛋白共价连接的外源Ad2 DNA的体外Ad2 DNA合成系统中发挥作用(池田等人,《美国国家科学院院刊》77:5827-5831,1980)。感染的CHO细胞质提取物能够补充未感染的CHO核提取物,以在Ad2模板上合成病毒DNA。这种体外复制系统有潜力探究宿主DNA合成需求以及病毒因子。