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Organisms with alternative genetic codes resolve unassigned codons via mistranslation and ribosomal rescue

机译:具有替代遗传密码的生物通过错误翻译和核糖体拯救来解析未分配的密码子

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Organisms possessing genetic codes with unassigned codons raise the question of how cellular machinery resolves such codons and how this could impact horizontal gene transfer. Here, we use a genomically recoded Escherichia coli to examine how organisms address translation at unassigned UAG codons, which obstruct propagation of UAG-containing viruses and plasmids. Using mass spectrometry, we show that recoded organisms resolve translation at unassigned UAG codons via near-cognate suppression, dramatic frameshifting from at least ?3 to +19 nucleotides, and rescue by ssrA -encoded tmRNA, ArfA, and ArfB. We then demonstrate that deleting tmRNA restores expression of UAG-ending proteins and propagation of UAG-containing viruses and plasmids in the recoded strain, indicating that tmRNA rescue and nascent peptide degradation is the cause of impaired virus and plasmid propagation. The ubiquity of tmRNA homologs suggests that genomic recoding is a promising path for impairing horizontal gene transfer and conferring genetic isolation in diverse organisms.
机译:拥有具有未分配密码子遗传密码的生物提出了一个问题,即细胞机制如何解析此类密码子,以及这如何影响水平基因转移。在这里,我们使用基因组重新编码的大肠杆菌来检查生物如何解决未分配的UAG密码子的翻译问题,这会阻碍包含UAG的病毒和质粒的繁殖。使用质谱法,我们显示经过重新编码的生物体通过近同源抑制,从至少?3到+19个核苷酸的显着移码以及通过ssrA编码的tmRNA,AlfA和ArfB进行拯救,可以解析未分配的UAG密码子的翻译。然后,我们证明删除tmRNA可以恢复UAG末端蛋白的表达以及包含UAG的病毒和质粒在编码菌株中的繁殖,这表明tmRNA的拯救和新生肽的降解是病毒和质粒繁殖受损的原因。 tmRNA同源物的普遍存在表明,基因组编码是削弱水平基因转移并赋予多种生物遗传隔离的一种有前途的途径。

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