Harper F, Florentin Y, Puvion E
EMBO J. 1984 Jun;3(6):1235-41. doi: 10.1002/j.1460-2075.1984.tb01958.x.
SV40 chromatin extracted from 42 h post-infected cells by a modification of the standard Triton X-100-EDTA procedure and purified on neutral sucrose gradients was partially immunoprecipitable by a specific SV40 T-antigen (T-Ag) antiserum. Electron microscopic observations of spread minichromosomes were made after labelling by the indirect colloidal gold immunological method using monoclonal antibodies specific for the SV40 T-Ag. In 1-2% of morphologically mature minichromosomes the labelling corresponding to tightly bound T-Ag was localized within the nucleosome-free region near one of its borders. Mapping with three single-cut restriction endonucleases: BamHI, EcoRI and BglI localized the labelling near to, or at the origin of, replication. In addition, we observed that the T-Ag specific antibodies were linked to a DNA-bound particle when the region was not masked by a large clump of antibodies. The variable size of this particle led us to suggest that it might be a complex of T-Ag with other proteins.
通过对标准的Triton X-100-EDTA程序进行改进,从感染后42小时的细胞中提取的SV40染色质,并在中性蔗糖梯度上进行纯化,其可被特异性的SV40 T抗原(T-Ag)抗血清部分免疫沉淀。使用针对SV40 T-Ag的单克隆抗体,通过间接胶体金免疫方法进行标记后,对伸展的微型染色体进行了电子显微镜观察。在1%-2%形态成熟的微型染色体中,与紧密结合的T-Ag相对应的标记位于其边界之一附近的无核小体区域内。用三种单切限制性内切酶:BamHI、EcoRI和BglI进行图谱分析,将标记定位在复制起点附近或复制起点处。此外,我们观察到,当该区域未被大量抗体团块掩盖时,T-Ag特异性抗体与一个DNA结合颗粒相连。该颗粒大小不一,这使我们推测它可能是T-Ag与其他蛋白质的复合物。