Bendig M M, Folk W R
J Virol. 1979 Nov;32(2):530-5. doi: 10.1128/JVI.32.2.530-535.1979.
Mutants of polyoma virus with deletions as large as 90 base pairs were isolated by selecting spontaneously arising genomes resistant to endonuclease HaeII or by treating HaeII- or BglI- cleaved linear DNAs with S1 nuclease and exonuclease III. All of the mutants were viable and, therefore, defined a nonessential region in the polyoma genome between the origin of DNA replication and the initiation codon for translation of early proteins. Several mutants with large deletions had altered growth properties, giving smaller plaques and lower virus yields than the parental wild-type virus. These viruses may lack sites that are important for DNA replication or for transcription and translation of early mRNA's. All of the mutants tested could transform BHK-21 cells to anchorage independence.
通过选择对核酸内切酶HaeII具有抗性的自发产生的基因组,或用S1核酸酶和核酸外切酶III处理经HaeII或BglI切割的线性DNA,分离出缺失多达90个碱基对的多瘤病毒突变体。所有突变体均具有活性,因此确定了多瘤病毒基因组中位于DNA复制起点和早期蛋白质翻译起始密码子之间的一个非必需区域。几个具有大缺失的突变体具有改变的生长特性,与亲本野生型病毒相比,产生的噬菌斑更小,病毒产量更低。这些病毒可能缺少对DNA复制或早期mRNA的转录和翻译很重要的位点。所有测试的突变体都能将BHK - 21细胞转化为不依赖贴壁生长。