Behm M, Lowman H, Ng S C, Bina M
Department of Chemistry, Purdue University, West Lafayette, IN 47907.
Proc Natl Acad Sci U S A. 1988 Dec;85(24):9421-5. doi: 10.1073/pnas.85.24.9421.
Temperature-sensitive (ts) assembly mutants of the tumorigenic virus simian virus 40 (SV40) fail to follow the normal pathway of virion morphogenesis at 40 degrees C. The mutations were previously mapped to the gene coding for the major virion protein VP1 and fall into three groups: tsB, tsBC, and tsC. We have determined the tsB/C mutations by DNA sequence analysis and deduced the corresponding amino acid substitutions. We find that the mutations are global and span 68% of the VP1 gene. They result predominantly in single amino acid substitutions. The B mutations are localized between nucleotides 1667 and 2091, spanning the VP1 amino acid residues 54-195. With the exception of one mutation in tsC260, the C group mutations occur between the nucleotides 2141 and 2262, spanning VP1 residues 212-252. The tsBC substitutions are not localized within a distinct region. We present a model for the VP1 structure. The model correlates the distribution of ts assembly mutations in the SV40 VP1 gene with the VP1 functional domains, deduced form the phenotypes exhibited by the assembly mutants, and the VP1 structural domains, deduced recently from the cryoelectron microscopic studies of the SV40 virions. We summarize the behavior of the SV40 ts mutants and discuss the possible relationship between the ts phenotype and amino acid substitutions.
致瘤病毒猿猴病毒40(SV40)的温度敏感(ts)装配突变体在40摄氏度时无法遵循病毒体形态发生的正常途径。这些突变先前已定位到编码主要病毒体蛋白VP1的基因上,并分为三组:tsB、tsBC和tsC。我们通过DNA序列分析确定了tsB/C突变,并推导了相应的氨基酸替换。我们发现这些突变是全局性的,跨越了VP1基因的68%。它们主要导致单个氨基酸替换。B组突变位于核苷酸1667和2091之间,跨越VP1氨基酸残基54 - 195。除了tsC260中的一个突变外,C组突变发生在核苷酸2141和2262之间,跨越VP1残基212 - 252。tsBC替换并不局限于一个特定区域。我们提出了一个VP1结构模型。该模型将SV40 VP1基因中ts装配突变的分布与VP1功能域相关联,VP1功能域是从装配突变体表现出的表型推导出来的,同时也与VP1结构域相关联,VP1结构域是最近从SV40病毒体的冷冻电子显微镜研究中推导出来的。我们总结了SV40 ts突变体的行为,并讨论了ts表型与氨基酸替换之间可能的关系。