Soeda E, Arrand J R, Smolar N, Griffin B E
Cell. 1979 Jun;17(2):357-70. doi: 10.1016/0092-8674(79)90162-4.
The sequence of about one third of the polyoma virus genome is presented. This sequence covers the origin of replication of two large plaque strains (A2 and A3) of polyoma virus. The two strains differ by 11 bp in the origin region. A model for replication is suggested. The sequence probably also covers the entire coding region of two of the polyoma virus early proteins--small and middle T antigens--as well as part of the coding region for large T antigen. Over a small region of the DNA, all three coding frames contain termination codons, which argues a need for spliced early messenger RNAs. In another region of the DNA, two coding frames can be used. Correlation with protein data suggests that one frame codes for part of middle T antigen and the other for part of large T antigen.
本文展示了约三分之一的多瘤病毒基因组序列。该序列涵盖了多瘤病毒两个大噬菌斑毒株(A2和A3)的复制起点。这两个毒株在起点区域相差11个碱基对。文中提出了一个复制模型。该序列可能还涵盖了多瘤病毒两种早期蛋白——小T抗原和中T抗原——的整个编码区域,以及大T抗原编码区域的一部分。在DNA的一个小区域内,所有三个编码框架都包含终止密码子,这表明需要剪接的早期信使RNA。在DNA的另一个区域,可以使用两个编码框架。与蛋白质数据的相关性表明,一个框架编码中T抗原的一部分,另一个编码大T抗原的一部分。