Uckert W, Grófová M, Beaudreau G
Virology. 1984 May;135(1):288-92. doi: 10.1016/0042-6822(84)90138-7.
The translational orders of bovine leukemia virus (BLV) gag proteins and env proteins have been determined by the technique of pactamycin mapping. BLV-producing fetal lamb kidney (FLK) cells were pulse-labeled with 14C amino acids and [3H]glucosamine in the presence or absence of pactamycin which inhibits initiation of protein synthesis but not elongation. Viruses were harvested from the cell culture medium and viral proteins were analyzed by SDS-polyacrylamide gel electrophoresis. For each protein the " pactamycin ratio" was determined. The lower this ratio was for a given protein, the closer the protein would be to the amino terminus of the precursor polyprotein. From these experiments the following translational orders were derived: gag, NH2-p10-(p15(2) X p15(1)-p24-p12-COOH; and env, NH2- gp64 - gp30 -COOH. Investigation of isoelectric points of BLV proteins, a conserved property of retroviral proteins, supported the translational order of gag gene-coded proteins.
通过嘌呤霉素定位技术确定了牛白血病病毒(BLV)gag蛋白和env蛋白的翻译顺序。在存在或不存在抑制蛋白质合成起始但不抑制延伸的嘌呤霉素的情况下,用14C氨基酸和[3H]葡糖胺对产生BLV的胎羊肾(FLK)细胞进行脉冲标记。从细胞培养基中收获病毒,并通过SDS-聚丙烯酰胺凝胶电泳分析病毒蛋白。对于每种蛋白,测定“嘌呤霉素比率”。给定蛋白的该比率越低,该蛋白就越靠近前体多蛋白的氨基末端。从这些实验中得出了以下翻译顺序:gag,NH2-p10-(p15(2)×p15(1)-p24-p12-COOH;以及env,NH2-gp64-gp30-COOH。对BLV蛋白等电点的研究(逆转录病毒蛋白的一种保守特性)支持了gag基因编码蛋白的翻译顺序。