Rothwell V M, Folk W R
J Virol. 1983 Nov;48(2):472-80. doi: 10.1128/JVI.48.2.472-480.1983.
The DNA sequence of two wild-type strains of polyomavirus (A2 and strain 3) are known. We have determined the majority of the DNA sequence of a third strain, the Crawford small-plaque virus. This virus has been noted for its capacity to induce readily detected tumor-specific transplantation antigen in hamster cells, a property that is most likely attributable to an altered middle T-antigen. A comparison of its DNA sequence with those of the A2 and strain 3 viruses reveals numerous nucleotide substitutions, insertions, and deletions throughout the genome. Most sequence changes in coding regions are silent mutations; however, variability in proteins can be predicted from these sequence data at 5 locations in middle T-antigen, 10 in large T-antigen, and 10 in VP1. The Crawford small-plaque virus noncoding regulatory region contains, in addition to nucleotide substitutions, a 44-base-pair tandem repeat of sequences on the late side of the origin of DNA replication.
多瘤病毒的两种野生型毒株(A2和毒株3)的DNA序列是已知的。我们已经确定了第三种毒株——克劳福德小斑块病毒的大部分DNA序列。这种病毒因其能够在仓鼠细胞中诱导易于检测到的肿瘤特异性移植抗原而闻名,这一特性很可能归因于中间T抗原的改变。将其DNA序列与A2和毒株3病毒的序列进行比较,发现整个基因组中有大量核苷酸替换、插入和缺失。编码区的大多数序列变化是沉默突变;然而,根据这些序列数据,可以预测中间T抗原的5个位置、大T抗原的10个位置和VP1的10个位置的蛋白质存在变异性。除了核苷酸替换外,克劳福德小斑块病毒的非编码调控区在DNA复制起点后期还包含一个44个碱基对的序列串联重复。