Frenkel G D
J Virol. 1978 Jan;25(1):459-63. doi: 10.1128/JVI.25.1.459-463.1978.
DNA-protein complexes isolated from adenovirus-infected cells by a modification of the M-band technique were used as an in vitro system for the study of adenovirus DNA replication. The synthesis in vitro was semiconservative, inhibited by N-ethylmaleimide, and stimulated by ATP. Studies on DNA-negative mutants of adenovirus showed that the DNA synthesis in vitro represents a continuation of adenovirus DNA replication in vivo. DNA synthesis in vitro was inhibited 38% by 20 microgram of phosphonoacetic acid per ml, which is several-fold higher than the inhibition obtained with purified DNA polymerase beta or gamma, but was similar to the degree of inhibition of DNA polymerase alpha. DNA synthesis in complexes from uninfected cells was much less sensitive to inhibition by phosphonoacetic acid. In addition, complexes from infected cells contained a greater proportion of the alpha-polymerase than complexes from uninfected cells, suggesting that an association of alpha-polymerase with the replication complex may be occurring during adenovirus infection, with subsequent utilization of the alpha-polymerase for viral DNA synthesis.
通过改良的M带技术从腺病毒感染细胞中分离出的DNA-蛋白质复合物,被用作研究腺病毒DNA复制的体外系统。体外合成是半保留的,受N-乙基马来酰亚胺抑制,并受ATP刺激。对腺病毒DNA阴性突变体的研究表明,体外DNA合成代表了腺病毒DNA在体内复制的延续。每毫升20微克的膦酰乙酸可抑制体外DNA合成38%,这比用纯化的DNA聚合酶β或γ所获得的抑制率高几倍,但与DNA聚合酶α的抑制程度相似。来自未感染细胞的复合物中的DNA合成对膦酰乙酸抑制的敏感性要低得多。此外,来自感染细胞的复合物中α-聚合酶的比例比来自未感染细胞的复合物中更高,这表明在腺病毒感染期间,α-聚合酶可能与复制复合物发生了关联,随后利用α-聚合酶进行病毒DNA合成。