Yen T S, Webster R E
Cell. 1982 Jun;29(2):337-45. doi: 10.1016/0092-8674(82)90150-7.
The gene II region of bacteriophage f1 DNA codes for two proteins, the 46 kd gene II protein and the 13 kd gene X protein, which results from an in-phase start at codon 300 of gene II. Using antigene II protein IgG, we show that the intracellular concentration of both proteins is controlled by the phage gene V protein. In wild-type f1-infected cells, the amount of gene II protein reaches a plateau of about 1500 molecules per cell at 20 min after infection, as measured by blot immunoassay. Similarly, the amount of gene X protein reaches a peak of about 500 molecules per cell around 10 min after infection. In contrast, when the gene V protein is inactive, both gene II and gene X proteins continue to accumulate at a high rate for at least 40 min after infection. This difference is caused by decreased synthesis of gene II and gene X proteins in the presence of gene V protein, which represses the translation of these two proteins.
噬菌体f1 DNA的基因II区域编码两种蛋白质,即46 kd的基因II蛋白和13 kd的基因X蛋白,后者由基因II第300位密码子处的同相位起始产生。使用抗基因II蛋白IgG,我们发现这两种蛋白质的细胞内浓度均受噬菌体基因V蛋白的控制。通过印迹免疫测定法测量,在野生型f1感染的细胞中,感染后20分钟时基因II蛋白的量达到每个细胞约1500个分子的稳定水平。同样,基因X蛋白的量在感染后约10分钟达到每个细胞约500个分子的峰值。相比之下,当基因V蛋白无活性时,感染后至少40分钟内基因II和基因X蛋白都继续以高速率积累。这种差异是由于在基因V蛋白存在的情况下基因II和基因X蛋白的合成减少所致,基因V蛋白会抑制这两种蛋白质的翻译。