Oliveira C C, McCarthy J E
Department of Gene Expression, National Biotechnology Research Center (GBF), Braunschweig, Federal Republic of Germany.
J Biol Chem. 1995 Apr 14;270(15):8936-43. doi: 10.1074/jbc.270.15.8936.
A new strategy was developed to study the relationship between the translation and degradation of a specific mRNA in the yeast Saccharomyces cerevisiae. A series of 5'-untranslated regions (UTR) was combined with the cat gene from the bacterial transposon Tn9, allowing us to test the influence of upstream open reading frames (uORFs) on translation and mRNA stability. The 5'-UTR sequences were designed so that the minimum possible sequence alteration, a single nucleotide substitution, could be used to create a 7-codon ORF upstream of the cat gene. The uORF was translated efficiently, but at the same time inhibited translation of the cat ORF and destabilized the cat mRNA. Investigations of various derivatives of the 5'-UTR indicated that cat translation was primarily attributable to leaky scanning of ribosomes past the uORF rather than to reinitiation. Therefore, these data directly demonstrate destabilization of a specific mRNA linked to changes in translational initiation on the same transcript. In contrast to the previously proposed nonsense-mediated mRNA decay pathway, destabilization was not triggered by premature translational termination in the main ORF and was not discernibly dependent upon a reinitiation-driven mechanism. This suggests the existence of an as yet not described pathway of translation-linked mRNA degradation.
我们开发了一种新策略来研究酿酒酵母中特定mRNA的翻译与降解之间的关系。一系列5'-非翻译区(UTR)与来自细菌转座子Tn9的cat基因相结合,使我们能够测试上游开放阅读框(uORF)对翻译和mRNA稳定性的影响。设计5'-UTR序列时,使得只需最少的序列改变(单个核苷酸替换),就能在cat基因上游创建一个7密码子的开放阅读框。该uORF能够高效翻译,但同时会抑制cat开放阅读框的翻译,并使cat mRNA不稳定。对5'-UTR各种衍生物的研究表明,cat的翻译主要归因于核糖体越过uORF的漏扫描,而非重新起始。因此,这些数据直接证明了特定mRNA的不稳定与同一转录本上翻译起始的变化有关。与先前提出的无义介导的mRNA衰变途径不同,不稳定并非由主要开放阅读框中的过早翻译终止触发,并且明显不依赖于重新起始驱动的机制。这表明存在一种尚未描述的与翻译相关的mRNA降解途径。