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具有替代遗传密码的生物体通过翻译错误和核糖体拯救来解决未分配密码子的问题。

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

机构信息

Department of Molecular, Cellular & Developmental Biology, Yale University, New Haven, United States.

Systems Biology Institute, Yale University, West Haven, United States.

出版信息

Elife. 2018 Oct 30;7:e34878. doi: 10.7554/eLife.34878.

Abstract

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 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 -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.

摘要

具有未分配密码子的遗传密码的生物体提出了这样一个问题,即细胞机制如何解决这些密码子,以及这可能如何影响水平基因转移。在这里,我们使用基因组重编码的方法来研究生物体如何解决未分配 UAG 密码子的翻译问题,这些密码子阻碍了 UAG 包含的病毒和质粒的传播。使用质谱法,我们表明,重编码的生物体通过近同功抑制、至少从-3 到+19 个核苷酸的显著移框以及由-编码的 tmRNA、ArfA 和 ArfB 进行挽救来解决未分配 UAG 密码子的翻译。然后,我们证明删除 tmRNA 可恢复 UAG 终止蛋白的表达以及 UAG 包含的病毒和质粒在重编码菌株中的传播,表明 tmRNA 挽救和新生肽降解是病毒和质粒传播受损的原因。tmRNA 同源物的普遍性表明,基因组重编码是一种有前途的方法,可以削弱水平基因转移并在不同生物体中赋予遗传隔离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d316/6207430/c36ed5afc813/elife-34878-fig1.jpg

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