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多胺是大肠杆菌 tRNA 反密码子修饰所必需的。

Polyamines are Required for tRNA Anticodon Modification in Escherichia coli.

机构信息

Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen, Denmark.

Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen, Denmark.

出版信息

J Mol Biol. 2021 Jul 23;433(15):167073. doi: 10.1016/j.jmb.2021.167073. Epub 2021 May 29.

Abstract

Biogenic polyamines are natural aliphatic polycations formed from amino acids by biochemical pathways that are highly conserved from bacteria to humans. Their cellular concentrations are carefully regulated and dysregulation causes severe cell growth defects. Polyamines have high affinity for nucleic acids and are known to interact with mRNA, tRNA and rRNA to stimulate the translational machinery, but the exact molecular mechanism(s) for this stimulus is still unknown. Here we exploit that Escherichia coli is viable in the absence of polyamines, including the universally conserved putrescine and spermidine. Using global macromolecule labelling approaches we find that ribosome efficiency is reduced by 50-70% in the absence of polyamines and this reduction is caused by slow translation elongation speed. The low efficiency causes rRNA and multiple tRNA species to be overproduced in the absence of polyamines, suggesting an impact on the feedback regulation of stable RNA transcription. Importantly, we find that polyamine deficiency affects both tRNA levels and tRNA modification patterns. Specifically, a large fraction of tRNA, tRNA and tRNA lack the queuosine modification in the anticodon "wobble" base, which can be reversed by addition of polyamines to the growth medium. In conclusion, we demonstrate that polyamines are needed for modification of specific tRNA, possibly by facilitating the interaction with modification enzymes.

摘要

生物源多胺是由氨基酸通过生物化学途径形成的天然脂肪族多阳离子,在从细菌到人高度保守。它们的细胞浓度受到严格调节,失调会导致严重的细胞生长缺陷。多胺与核酸具有高亲和力,已知与 mRNA、tRNA 和 rRNA 相互作用以刺激翻译机制,但这种刺激的确切分子机制尚不清楚。在这里,我们利用大肠杆菌在缺乏多胺的情况下仍然能够存活这一事实,包括普遍存在的腐胺和精胺。我们使用全局大分子标记方法发现,在缺乏多胺的情况下,核糖体效率降低了 50-70%,这种降低是由于翻译延伸速度缓慢所致。低效率导致 rRNA 和多种 tRNA 过度产生,表明对稳定 RNA 转录的反馈调节有影响。重要的是,我们发现多胺缺乏会影响 tRNA 水平和 tRNA 修饰模式。具体来说,很大一部分 tRNA、tRNA 和 tRNA 在反密码子“摆动”碱基处缺乏 queuosine 修饰,在生长培养基中添加多胺可以逆转这种修饰。总之,我们证明了多胺对于特定 tRNA 的修饰是必需的,这可能是通过促进与修饰酶的相互作用来实现的。

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