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tRNA 第 55 位假尿嘧啶核苷控制着其他修饰核苷酸的含量,从而实现极端嗜热真细菌 Thermus thermophilus 在低温下的适应。

Pseudouridine at position 55 in tRNA controls the contents of other modified nucleotides for low-temperature adaptation in the extreme-thermophilic eubacterium Thermus thermophilus.

机构信息

Department of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, Bunkyo 3, Matsuyama, Ehime 790-8577, Japan.

出版信息

Nucleic Acids Res. 2011 Mar;39(6):2304-18. doi: 10.1093/nar/gkq1180. Epub 2010 Nov 18.

DOI:10.1093/nar/gkq1180
PMID:21097467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3064792/
Abstract

Pseudouridine at position 55 (Ψ55) in eubacterial tRNA is produced by TruB. To clarify the role of the Ψ55 modification, we constructed a truB gene disruptant (ΔtruB) strain of Thermus thermophilus which is an extreme-thermophilic eubacterium. Unexpectedly, the ΔtruB strain exhibited severe growth retardation at 50 °C. We assumed that these phenomena might be caused by lack of RNA chaperone activity of TruB, which was previously hypothetically proposed by others. To confirm this idea, we replaced the truB gene in the genome with mutant genes, which express TruB proteins with very weak or no enzymatic activity. However the growth retardation at 50 °C was not rescued by these mutant proteins. Nucleoside analysis revealed that Gm18, m(5)s(2)U54 and m(1)A58 in tRNA from the ΔtruB strain were abnormally increased. An in vitro assay using purified tRNA modification enzymes demonstrated that the Ψ55 modification has a negative effect on Gm18 formation by TrmH. These experimental results show that the Ψ55 modification is required for low-temperature adaptation to control other modified. (35)S-Met incorporation analysis showed that the protein synthesis activity of the ΔtruB strain was inferior to that of the wild-type strain and that the cold-shock proteins were absence in the ΔtruB cells at 50°C.

摘要

在原核生物 tRNA 中的 55 位假尿嘧啶(Ψ55)是由 TruB 产生的。为了阐明 Ψ55 修饰的作用,我们构建了嗜热栖热菌(Thermus thermophilus)的 truB 基因敲除(ΔtruB)菌株,这是一种极端嗜热的原核生物。出乎意料的是,ΔtruB 菌株在 50°C 时表现出严重的生长迟缓。我们假设这些现象可能是由于 TruB 的 RNA 伴侣活性缺失所致,这是其他人之前假设的。为了证实这一观点,我们用突变基因替换了基因组中的 truB 基因,这些突变基因表达的 TruB 蛋白具有非常弱或没有酶活性。然而,这些突变蛋白并不能挽救 50°C 时的生长迟缓。核苷分析表明,ΔtruB 菌株 tRNA 中的 Gm18、m(5)s(2)U54 和 m(1)A58 异常增加。使用纯化的 tRNA 修饰酶进行的体外测定表明,Ψ55 修饰对 TrmH 形成 Gm18 具有负效应。这些实验结果表明,Ψ55 修饰是适应低温所必需的,以控制其他修饰。(35)S-甲硫氨酸掺入分析表明,ΔtruB 菌株的蛋白质合成活性低于野生型菌株,并且在 50°C 时ΔtruB 细胞中不存在冷休克蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/d8b02ac3e231/gkq1180f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/b0623ce3e65d/gkq1180f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/185a042a8247/gkq1180f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/da3730fb9c3e/gkq1180f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/20da1551c33a/gkq1180f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/d8b02ac3e231/gkq1180f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/b0623ce3e65d/gkq1180f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/80b61582a7f4/gkq1180f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/5e39f1de4dbd/gkq1180f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/30f087328cdd/gkq1180f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/185a042a8247/gkq1180f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/da3730fb9c3e/gkq1180f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/74d3c6afd5fd/gkq1180f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/20da1551c33a/gkq1180f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d193/3064792/d8b02ac3e231/gkq1180f9.jpg

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