Svensson C, Akusjärvi G
EMBO J. 1985 Apr;4(4):957-64. doi: 10.1002/j.1460-2075.1985.tb03724.x.
The effect of adenovirus VA RNAI on the translation of mRNAs expressing the bacterial chloramphenicol acetyltransferase (CAT) enzyme was studied by a transient expression assay in 293 cells. The CAT activity was determined in extracts prepared from cells transfected with mixtures of plasmids encoding CAT and VA RNA. The results showed that VA RNAI co-transfection resulted in a significant increase in CAT expression from a variety of constructs. Thus, expression of CAT from a SV40 mRNA, a beta-globin mRNA and a chimeric mRNA containing the adenovirus-2 tripartite leader were all stimulated approximately 6-fold by VA RNAI. Based on these results we conclude that the tripartite leader sequence is not required for the VA RNA-mediated stimulation of translation. Our results indicate instead that VA RNAI probably functions as a general enhancer of mRNA translation. A2- to 3-fold stimulation of CAT expression was also obtained following transient expression of HeLa and CV-1 cells. The reduced efficiency was correlated with a 10- to 20-fold lower level of VA RNA expression in HeLa compared with 293 cells. Thus, it is likely that a product from region E1 indirectly enhances the translational efficiency by stimulating VA RNA transcription.
通过在293细胞中进行瞬时表达分析,研究了腺病毒VA RNAI对表达细菌氯霉素乙酰转移酶(CAT)的mRNA翻译的影响。在用编码CAT和VA RNA的质粒混合物转染的细胞制备的提取物中测定CAT活性。结果表明,共转染VA RNAI导致多种构建体的CAT表达显著增加。因此,来自SV40 mRNA、β-珠蛋白mRNA和含有腺病毒2型三联前导序列的嵌合mRNA的CAT表达均被VA RNAI刺激了约6倍。基于这些结果,我们得出结论,VA RNA介导的翻译刺激不需要三联前导序列。相反,我们的结果表明VA RNAI可能作为mRNA翻译的一般增强子发挥作用。在HeLa和CV-1细胞瞬时表达后,也获得了2至3倍的CAT表达刺激。效率降低与HeLa中VA RNA表达水平比293细胞低10至20倍相关。因此,E1区的产物可能通过刺激VA RNA转录间接提高翻译效率。