Garcia-Moreno Manuel, Sanz Miguel Angel, Carrasco Luis
Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), C/Nicolás Cabrera 1, Universidad Autónoma de Madrid, Cantoblanco, Madrid 28049, Spain
Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), C/Nicolás Cabrera 1, Universidad Autónoma de Madrid, Cantoblanco, Madrid 28049, Spain.
RNA. 2015 Jan;21(1):93-112. doi: 10.1261/rna.047084.114. Epub 2014 Nov 17.
Translation initiation of alphavirus subgenomic mRNA (sgmRNA) can occur in the absence of several initiation factors (eIFs) in infected cells; however, the precise translation mechanism is still poorly understood. In this study, we have examined the mechanism of initiation and AUG selection in Sindbis virus (SINV) sgmRNA. Our present findings suggest that sgmRNA is translated via a scanning mechanism, since the presence of a hairpin structure before the initiation codon hampers protein synthesis directed by this mRNA. In addition, translation is partially recovered when an in-frame AUG codon is placed upstream of this hairpin. This scanning process takes place without the participation of eIF4A and active eIF2. These results, combined with our findings through modifying the SINV sgmRNA leader sequence, do not support the possibility of a direct initiation from the start codon without previous scanning, or a shunting mechanism. Moreover, studies carried out with sgmRNAs containing two alternative AUG codons within a good context for translation reveal differences in AUG selection which are dependent on the cellular context and the phosphorylation state of eIF2α. Thus, initiation at the additional AUG is strictly dependent on active eIF2, whereas the genuine AUG codon can start translation following eIF2α inactivation. Collectively, our results suggest that SINV sgmRNA is translated by a scanning mechanism without the potential participation of crucial eIFs. A model is presented that explains the mechanism of initiation of mRNAs bearing two alternative initiation codons.
甲病毒亚基因组mRNA(sgmRNA)的翻译起始可以在受感染细胞中缺乏几种起始因子(eIFs)的情况下发生;然而,其精确的翻译机制仍知之甚少。在本研究中,我们研究了辛德毕斯病毒(SINV)sgmRNA的起始和AUG选择机制。我们目前的研究结果表明,sgmRNA是通过扫描机制进行翻译的,因为起始密码子之前存在发夹结构会阻碍该mRNA指导的蛋白质合成。此外,当一个符合读框的AUG密码子置于该发夹结构上游时,翻译会部分恢复。这种扫描过程在没有eIF4A和活性eIF2参与的情况下发生。这些结果,结合我们通过修改SINV sgmRNA前导序列的研究结果,不支持在没有先前扫描的情况下直接从起始密码子起始或跳跃机制的可能性。此外,对在良好翻译背景下含有两个可供选择的AUG密码子的sgmRNA进行的研究揭示了AUG选择的差异,这些差异取决于细胞背景和eIF2α的磷酸化状态。因此,在额外AUG处的起始严格依赖于活性eIF2,而真正的AUG密码子可以在eIF2α失活后开始翻译。总的来说,我们的结果表明SINV sgmRNA是通过扫描机制进行翻译的,关键的eIFs可能不参与其中。本文提出了一个模型,解释了带有两个可供选择的起始密码子的mRNA的起始机制。