López de Quinto S, Martínez-Salas E
Consejo Superior de Investigaciones Científicas-, Universidad Autónoma de Madrid, Madrid, Cantoblanco, 28049, Spain.
Virology. 1999 Mar 15;255(2):324-36. doi: 10.1006/viro.1999.9598.
Initiation of translation in picornavirus RNAs occurs internally, mediated by an element termed internal ribosome entry site (IRES). In the aphthovirus RNA, the IRES element directs translation initiation at two in-frame AUGs separated by 84 nucleotides. We have found that bicistronic constructs that contained the IRES element followed by the fragment including the aphthovirus start codons in front of the second gene mimicked the translation initiation pattern of viral RNA observed in infected cells. In those constructs, the frequency of initiation at the first AUG was increased by a sequence context that resembled the favorable consensus for cap-dependent translation, although initiation at the second site was always preferred. In addition, we have found that initiation at the second start codon was not diminished under conditions in which the first initiation codon was blocked by antisense oligonucleotide interference. Interestingly, mutations that positioned the second AUG out-of-frame with the first AUG did not interfere with the frequency of initiation at the second one. On the contrary, IRES-dependent translation initiation in bicistronic constructs lacking the sequences present between functional AUGs in the viral RNA was sensitive to the presence of out-of-frame initiator codons and hairpins in the spacer region. This remarkable difference in start codon recognition was due to the nucleotide composition of the RNA that separated the IRES from the initiator codon. Thus our results indicate that the region located in the aphthovirus RNA between functional AUGs is involved in start codon recognition, strongly favoring selection of the second start AUG as the main initiator codon.
小核糖核酸病毒RNA的翻译起始发生在内部,由一种称为内部核糖体进入位点(IRES)的元件介导。在口蹄疫病毒RNA中,IRES元件指导在两个读框内的AUG处起始翻译,这两个AUG相隔84个核苷酸。我们发现,双顺反子构建体包含IRES元件,其后是第二个基因前面包含口蹄疫病毒起始密码子的片段,该构建体模仿了在感染细胞中观察到的病毒RNA的翻译起始模式。在那些构建体中,第一个AUG处的起始频率因一个类似于帽依赖性翻译的有利共有序列的序列上下文而增加,尽管第二个位点的起始总是更受青睐。此外,我们发现,在第一个起始密码子被反义寡核苷酸干扰阻断的条件下,第二个起始密码子的起始并未减少。有趣的是,使第二个AUG与第一个AUG不在同一读框内的突变并不影响第二个AUG处的起始频率。相反,在病毒RNA中缺乏功能性AUG之间存在的序列的双顺反子构建体中,依赖IRES的翻译起始对间隔区中不在读框内的起始密码子和发夹的存在敏感。起始密码子识别上的这种显著差异是由于将IRES与起始密码子分开的RNA的核苷酸组成。因此,我们的结果表明,口蹄疫病毒RNA中位于功能性AUG之间的区域参与起始密码子识别,强烈倾向于选择第二个起始AUG作为主要起始密码子。