Barker G F, Beemon K
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
Mol Cell Biol. 1991 May;11(5):2760-8. doi: 10.1128/mcb.11.5.2760-2768.1991.
The intracellular accumulation of the unspliced RNA of Rous sarcoma virus was decreased when translation was prematurely terminated by the introduction of nonsense codons within its 5' proximal gene, the gag gene. In contrast, the levels of spliced viral RNAs were not affected in our transient expression assays in chicken cells. Experiments using the transcription inhibitor dactinomycin showed that mutant unspliced RNAs were degraded more rapidly than wild-type RNA. Furthermore, mutant RNAs could be partially stabilized by coexpression of wild-type gag proteins in trans; however, intact gag proteins were not required to maintain the stability of RNAs which did not contain premature termination codons. Thus, termination codons seemed to destabilize the RNA not because of their effect on gag protein function but instead because they disrupted the process of translating the gag region of the RNA. Analysis of double-mutant constructs containing both deletions and termination codons within the gag gene also suggested that the stability of the unspliced RNA was affected by a cis-acting interaction between the RNA and ribosomes.
当通过在劳斯肉瘤病毒5'近端基因(gag基因)内引入无义密码子使翻译提前终止时,该病毒未剪接RNA的细胞内积累量会减少。相比之下,在我们对鸡细胞进行的瞬时表达试验中,剪接后的病毒RNA水平并未受到影响。使用转录抑制剂放线菌素进行的实验表明,突变的未剪接RNA比野生型RNA降解得更快。此外,通过反式共表达野生型gag蛋白,突变RNA可以得到部分稳定;然而,维持不含提前终止密码子的RNA的稳定性并不需要完整的gag蛋白。因此,终止密码子似乎使RNA不稳定,并非因为它们对gag蛋白功能有影响,而是因为它们破坏了RNA的gag区域的翻译过程。对在gag基因内同时含有缺失和终止密码子的双突变构建体的分析也表明,未剪接RNA的稳定性受到RNA与核糖体之间顺式作用相互作用的影响。