Butnick N Z, Miyamoto C, Chizzonite R, Cullen B R, Ju G, Skalka A M
Mol Cell Biol. 1985 Nov;5(11):3009-16. doi: 10.1128/mcb.5.11.3009-3016.1985.
The influence of untranslated 5' sequences on c-myc expression was compared by measuring the translational efficiencies of mRNAs which contain leaders derived from exon 1 or intron 1 of the human c-myc gene. Expression plasmids were constructed and introduced into COS cells, and the levels of c-myc mRNA and protein were examined. Our results show that mRNAs transcribed from constructs containing exon 1 or intron 1, which have different folding potential, are translated with approximately equal efficiencies. This suggests that the translation of c-myc mRNA is not controlled by secondary structure alone. In addition, we observed that transcripts in which exon 1 was deleted are not translated more efficiently, but are present at a higher steady-state level. Thus, this example provides evidence for possible control at the transcriptional level. Finally, since the c-myc product was produced in each of our test systems, the results suggest that this protein does not regulate its own transcription or translation via a specific interaction with c-myc exon 1 alone.
通过测量含有源自人c-myc基因外显子1或内含子1的前导序列的mRNA的翻译效率,比较了未翻译的5'序列对c-myc表达的影响。构建表达质粒并导入COS细胞,检测c-myc mRNA和蛋白质的水平。我们的结果表明,从含有具有不同折叠潜力的外显子1或内含子1的构建体转录的mRNA以大致相等的效率进行翻译。这表明c-myc mRNA的翻译并非仅受二级结构控制。此外,我们观察到外显子1缺失的转录本翻译效率并未提高,但在稳态水平上含量更高。因此,该实例为转录水平的可能调控提供了证据。最后,由于在我们的每个测试系统中都产生了c-myc产物,结果表明该蛋白质并非仅通过与c-myc外显子1的特异性相互作用来调节其自身的转录或翻译。