Milon Pohl, Konevega Andrey L, Gualerzi Claudio O, Rodnina Marina V
Department of Biology MCA, Laboratory of Genetics, University of Camerino, 62032 Camerino, Italy.
Mol Cell. 2008 Jun 20;30(6):712-20. doi: 10.1016/j.molcel.2008.04.014.
The translation initiation efficiency of a given mRNA is determined by its translation initiation region (TIR). mRNAs are selected into 30S initiation complexes according to the strengths of the secondary structure of the TIR, the pairing of the Shine-Dalgarno sequence with 16S rRNA, and the interaction between initiator tRNA and the start codon. Here, we show that the conversion of the 30S initiation complex into the translating 70S ribosome constitutes another important mRNA control checkpoint. Kinetic analysis reveals that 50S subunit joining and dissociation of IF3 are strongly influenced by the nature of the codon used for initiation and the structural elements of the TIR. Coupling between the TIR and the rate of 70S initiation complex formation involves IF3- and IF1-induced rearrangements of the 30S subunit, providing a mechanism by which the ribosome senses the TIR and determines the efficiency of translational initiation of a particular mRNA.
给定mRNA的翻译起始效率由其翻译起始区域(TIR)决定。mRNA根据TIR二级结构的强度、Shine-Dalgarno序列与16S rRNA的配对以及起始tRNA与起始密码子之间的相互作用被选入30S起始复合物。在此,我们表明30S起始复合物向正在翻译的70S核糖体的转变构成了另一个重要的mRNA控制检查点。动力学分析表明,50S亚基的加入和IF3的解离受到起始所用密码子的性质和TIR结构元件的强烈影响。TIR与70S起始复合物形成速率之间的偶联涉及IF3和IF1诱导的30S亚基重排,提供了一种核糖体感知TIR并确定特定mRNA翻译起始效率的机制。