Deatly A M, Ben-Porat T
Virology. 1985 Jun;143(2):558-68. doi: 10.1016/0042-6822(85)90394-0.
Virus proteins synthesized by pseudorabies virus-infected cells can be classified into five groups on the basis of the kinetics of their synthesis at various stages of the infective process; virus mRNAs can similarly be classified into four groups. To determine whether the kinetics of synthesis of specific proteins are determined solely by the level of abundance in the cells of their mRNAs, we have compared at various times after infection the relative synthesis of these proteins with the relative abundance of their mRNAs. We have focused on two proteins: the 142K major capsid protein, an early-late protein, and the 136K major DNA binding protein, an early protein. The mRNAs encoding these proteins were identified. The relative abundances of these mRNAs in the cytoplasms of the infected cells were found to be the same as those associated with the polysome fractions. The relative amount of the proteins synthesized by the infected cells at a given stage of the infective process closely reflected the relative amount of the mRNA encoding these proteins that was present in the cells at that stage of the infective process. Most virus mRNA species that are present in the cytoplasm of infected cells were represented on polysomes to approximately an equal extent. Some RNA species were, however, significantly underrepresented under certain conditions in the polysomal fractions. We conclude that whereas the amount of many virus proteins synthesized by the infected cells is determined mainly by the level of the abundance of their mRNAs, additional controls operate in the cells that determine the relative rates of synthesis of some other virus proteins.
由伪狂犬病病毒感染细胞合成的病毒蛋白,根据其在感染过程不同阶段的合成动力学可分为五类;病毒mRNA同样可分为四类。为了确定特定蛋白的合成动力学是否仅由其mRNA在细胞中的丰度水平决定,我们在感染后的不同时间比较了这些蛋白的相对合成量与其mRNA的相对丰度。我们重点研究了两种蛋白:142K主要衣壳蛋白,一种早期-晚期蛋白,以及136K主要DNA结合蛋白,一种早期蛋白。编码这些蛋白的mRNA已被鉴定。发现这些mRNA在感染细胞胞质中的相对丰度与多核糖体组分中的相同。在感染过程的给定阶段,感染细胞合成的蛋白的相对量密切反映了在该感染阶段细胞中编码这些蛋白的mRNA的相对量。存在于感染细胞胞质中的大多数病毒mRNA种类在多核糖体上的占比大致相等。然而,在某些条件下,一些RNA种类在多核糖体组分中的占比明显偏低。我们得出结论,虽然感染细胞合成的许多病毒蛋白的量主要由其mRNA的丰度水平决定,但细胞中还存在其他调控机制,决定了一些其他病毒蛋白的相对合成速率。