Ishimi Y, Sugasawa K, Hanaoka F, Kikuchi A
Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
J Biol Chem. 1991 Aug 25;266(24):16141-8.
SV40 chromosomes prepared from infected CV-1 cells were replicated with the purified proteins of SV40 T antigen, HeLa DNA polymerase alpha-primase complex, single-stranded DNA-binding protein, and topoisomerases I and II, all of which have been shown to be essential for SV40 DNA replication in vitro. Replication started near the origin and proceeded bidirectionally. The maximum speed of replication fork movement was 200-300 nucleotides/min, which was similar to the rate of SV40 DNA replication with the same set of proteins. When replication products were digested with micrococcal nuclease, DNA fragments of 160-180 base pairs, which is the typical size of mononucleosomal DNA, were protected. This result indicates that replicated DNA was reconstructed into the nucleosome structure, complexed with parental histones.
从感染的CV - 1细胞中制备的SV40染色体,与SV40 T抗原、HeLa DNA聚合酶α - 引发酶复合物、单链DNA结合蛋白以及拓扑异构酶I和II的纯化蛋白一起进行复制,所有这些蛋白已被证明在体外对SV40 DNA复制至关重要。复制从起始点附近开始并双向进行。复制叉移动的最大速度为200 - 300个核苷酸/分钟,这与使用相同蛋白组进行SV40 DNA复制的速率相似。当用微球菌核酸酶消化复制产物时,160 - 180个碱基对的DNA片段受到保护,这是单核小体DNA的典型大小。该结果表明复制的DNA被重建为核小体结构,并与亲本组蛋白复合。