Sugasawa K, Murakami Y, Miyamoto N, Hanaoka F, Ui M
Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
J Virol. 1990 Oct;64(10):4820-9. doi: 10.1128/JVI.64.10.4820-4829.1990.
A soluble system was developed that could support DNA replication in simian virus 40 (SV40) chromosomes. DNA synthesis in this system required the presence of purified SV40 large tumor antigen, SV40 chromosomes prepared from virus-infected monkey cells, a crude extract from HeLa cells, and several low-molecular-weight components. In comparison to the replication of purified SV40 form I DNA, the rate of DNA synthesis was 15 to 20% in this system. DNA synthesis started near the replication origin of SV40 and proceeded bidirectionally in a semiconservative manner. Micrococcal nuclease digestion experiments revealed that the replicated DNA produced in this system became organized into a regularly spaced array of nucleosome core particles when an appropriate amount of purified HeLa core histones was added to the reaction mixture. SV40 form I DNA replicating under the same conditions was also assembled into nucleosomes, which were arranged in a rather dispersed manner and formed an aberrant chromatin structure.
开发了一种可支持猿猴病毒40(SV40)染色体中DNA复制的可溶性系统。该系统中的DNA合成需要纯化的SV40大T抗原、从病毒感染的猴细胞中制备的SV40染色体、来自HeLa细胞的粗提物以及几种低分子量成分。与纯化的SV40 I型DNA的复制相比,该系统中DNA合成的速率为15%至20%。DNA合成始于SV40的复制起点附近,并以半保留方式双向进行。微球菌核酸酶消化实验表明,当向反应混合物中加入适量纯化的HeLa核心组蛋白时,该系统中产生的复制DNA会组装成规则间隔排列的核小体核心颗粒。在相同条件下复制的SV40 I型DNA也会组装成核小体,这些核小体排列较为分散,形成异常的染色质结构。