Katinka M, Yaniv M
J Virol. 1983 Jul;47(1):244-8. doi: 10.1128/JVI.47.1.244-248.1983.
We constructed a series of deleted polyoma genomes by Bal 31 nuclease digestion from the unique Bg/I site at nucleotide 86 on the "early" side of the origin of DNA replication. The ability of the cloned deleted genomes to replicate was tested after transfection into mouse 3T6 fibroblasts or into the polyomatransformed C127 (COP5) mouse cell line (Tyndall et al., Nucleic Acids Res. 9:6231-6251, 1981). Deletions up to nucleotide 64-had no effect on the amount of replicated DNA accumulated, but larger deletions, extending up to nucleotide 42, decreased this amount 7- to 10-fold. By nucleotide 38, the quantity of detected DNA was down 100-fold, and by nucleotide 20, no replication could be detected. The minimum origin segment does not contain any known high-affinity, large tumor antigen binding site.
我们通过Bal 31核酸酶从DNA复制起点“早期”一侧核苷酸86处的独特Bg/I位点进行消化,构建了一系列缺失的多瘤病毒基因组。将克隆的缺失基因组转染到小鼠3T6成纤维细胞或多瘤病毒转化的C127(COP5)小鼠细胞系中后,测试其复制能力(廷德尔等人,《核酸研究》9:6231 - 6251,1981)。直至核苷酸64的缺失对积累的复制DNA量没有影响,但更大的缺失,延伸至核苷酸42,使该量减少了7至10倍。到核苷酸38时,检测到的DNA量下降了100倍,到核苷酸20时,无法检测到复制。最小的起始片段不包含任何已知的高亲和力大肿瘤抗原结合位点。