Stillman B
Cell. 1986 May 23;45(4):555-65. doi: 10.1016/0092-8674(86)90287-4.
A cytosol extract from human 293 cells supports efficient replication of SV40 origin-containing plasmid DNA in the presence of the SV40 T antigen. Addition of a nuclear extract from the same cells promotes negative supercoiling of the replicated DNA but not the bulk of the unreplicated DNA. The level of superhelicity is affected by the concentrations of T antigen and nuclear extract factors and by the time of addition of the nuclear extract. The replicated DNA in isolated DNA-protein complexes resists relaxation by purified HeLa cell topoisomerase I. Micrococcal nuclease digestion, sucrose gradient sedimentation, and electron microscopy demonstrate that the negative supercoils result from assembly of the replicating DNA into a chromatin structure. These results suggest that, during DNA replication, the core histones can be assembled on both sides of the replication fork by an active, replication-linked mechanism that does not require a template of preexisting nucleosomes.
在存在猴空泡病毒40(SV40)T抗原的情况下,来自人293细胞的胞质溶胶提取物能支持含SV40复制起点的质粒DNA高效复制。添加来自相同细胞的核提取物可促进复制DNA的负超螺旋形成,但对大部分未复制DNA则无此作用。超螺旋程度受T抗原和核提取物因子的浓度以及核提取物添加时间的影响。分离的DNA - 蛋白质复合物中的复制DNA可抵抗纯化的HeLa细胞拓扑异构酶I介导的松弛作用。微球菌核酸酶消化、蔗糖梯度沉降和电子显微镜观察表明,负超螺旋是由于复制DNA组装成染色质结构所致。这些结果表明,在DNA复制过程中,核心组蛋白可通过一种活跃的、与复制相关的机制在复制叉两侧组装,该机制不需要预先存在的核小体模板。