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A Leaderless mRNA Can Bind to Mammalian 80S Ribosomes and Direct Polypeptide Synthesis in the Absence of Translation Initiation Factors

机译:无领导者的mRNA可以绑定到哺乳动物80S核糖体和没有翻译起始因子的情况下直接多肽合成。

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摘要

Translation initiation in eukaryotic cells is known to be a complex multistep process which involves numerous protein factors. Here we demonstrate that leaderless mRNAs with initiator Met-tRNA can bind directly to 80S mammalian ribosomes in the absence of initiation factors and that the complexes thus formed are fully competent for the subsequent steps of polypeptide synthesis. We show that the canonical 48S pathway of eukaryotic translation initiation has no obvious advantage over the 80S pathway of translation initiation on leaderless mRNAs and suggest that, in the presence of competing mRNAs containing a leader, the latter mechanism will be preferred. The direct binding of the leaderless mRNA to the 80S ribosome was precluded when such an mRNA was supplied with a 5′ leader, irrespective of whether it was in a totally single-stranded conformation or was prone to base pairing. The striking similarity between the mechanisms of binding of leaderless mRNAs with mammalian 80S or bacterial 70S ribosomes gives support to the idea that the alternative mode of translation initiation used by leaderless mRNAs represents a relic from early steps in the evolution of the translation apparatus.
机译:真核细胞中的翻译起始是一个复杂的多步骤过程,涉及许多蛋白质因子。在这里,我们证明具有启动子Met-tRNA的无前导mRNA可以在没有启动因子的情况下直接与80S哺乳动物核糖体结合,因此形成的复合物完全可以胜任多肽合成的后续步骤。我们显示真核翻译起始的规范的48S途径比无引线的mRNA的翻译起始的80S途径没有明显的优势,并表明在存在包含一个引导子的竞争性mRNA的情况下,后一种机制将是优选的。当给该mRNA提供5'前导序列时,就排除了无前导序列mRNA与80S核糖体的直接结合,而不论其是完全单链构型还是易于碱基配对。无引线mRNA与哺乳动物80S或细菌70S核糖体结合的机制之间惊人的相似性,为无引线mRNA使用的另一种翻译起始模式代表了翻译设备发展早期阶段的遗迹提供了支持。

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