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J Bacteriol. 2009 Oct;191(19):6157-66. doi: 10.1128/JB.00699-09. Epub 2009 Jul 24.
2
A Stress-Induced Bias in the Reading of the Genetic Code in Escherichia coli.大肠杆菌中应激诱导的遗传密码阅读偏差。
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Selective translation of leaderless mRNAs by specialized ribosomes generated by MazF in Escherichia coli.在大肠杆菌中,由 MazF 产生的无帽 mRNA 特异性核糖体进行无帽 mRNA 的选择性翻译。
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A Stress-Induced Bias in the Reading of the Genetic Code in Escherichia coli.大肠杆菌中应激诱导的遗传密码阅读偏差。
mBio. 2016 Nov 15;7(6):e01855-16. doi: 10.1128/mBio.01855-16.
2
tRNA is a new target for cleavage by a MazF toxin.转运RNA是马兹F毒素切割的新靶点。
Nucleic Acids Res. 2016 Feb 18;44(3):1256-70. doi: 10.1093/nar/gkv1370. Epub 2016 Jan 5.
3
In vivo tmRNA protection by SmpB and pre-ribosome binding conformation in solution.体内SmpB对tmRNA的保护作用及溶液中前核糖体的结合构象。
RNA. 2014 Oct;20(10):1607-20. doi: 10.1261/rna.045674.114. Epub 2014 Aug 18.
4
An RNA-seq method for defining endoribonuclease cleavage specificity identifies dual rRNA substrates for toxin MazF-mt3.一种用于定义核糖核酸内切酶切割特异性的RNA测序方法鉴定出毒素MazF-mt3的双重rRNA底物。
Nat Commun. 2014 Apr 8;5:3538. doi: 10.1038/ncomms4538.
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23S rRNA as an a-Maz-ing new bacterial toxin target.23S rRNA 作为一种令人惊叹的新型细菌毒素靶标。
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Mycobacterial toxin MazF-mt6 inhibits translation through cleavage of 23S rRNA at the ribosomal A site.分枝杆菌毒素 MazF-mt6 通过在核糖体 A 位切割 23S rRNA 来抑制翻译。
Proc Natl Acad Sci U S A. 2013 May 21;110(21):8501-6. doi: 10.1073/pnas.1222031110. Epub 2013 May 6.
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The tmRNA ribosome-rescue system.tRNA 核糖体救援系统。
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8
Selective translation of leaderless mRNAs by specialized ribosomes generated by MazF in Escherichia coli.在大肠杆菌中,由 MazF 产生的无帽 mRNA 特异性核糖体进行无帽 mRNA 的选择性翻译。
Cell. 2011 Sep 30;147(1):147-57. doi: 10.1016/j.cell.2011.07.047. Epub 2011 Sep 22.
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In vivo safety and persistence of endoribonuclease gene-transduced CD4+ T cells in cynomolgus macaques for HIV-1 gene therapy model.在 HIV-1 基因治疗模型中,经内核糖核酸酶基因转导的 CD4+ T 细胞在食蟹猴体内的安全性和持久性。
PLoS One. 2011;6(8):e23585. doi: 10.1371/journal.pone.0023585. Epub 2011 Aug 17.
10
Crystallization of the Staphylococcus aureus MazF mRNA interferase.金黄色葡萄球菌MazF mRNA干扰酶的结晶
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Mar 1;67(Pt 3):386-9. doi: 10.1107/S1744309111000571. Epub 2011 Feb 25.

本文引用的文献

1
mRNA interferases, sequence-specific endoribonucleases from the toxin-antitoxin systems.信使核糖核酸干扰酶,来自毒素-抗毒素系统的序列特异性核糖核酸内切酶。
Prog Mol Biol Transl Sci. 2009;85:467-500. doi: 10.1016/S0079-6603(08)00812-X.
2
The mRNA interferases, MazF-mt3 and MazF-mt7 from Mycobacterium tuberculosis target unique pentad sequences in single-stranded RNA.来自结核分枝杆菌的mRNA干扰酶MazF-mt3和MazF-mt7靶向单链RNA中的独特五联体序列。
Mol Microbiol. 2008 Aug;69(3):559-69. doi: 10.1111/j.1365-2958.2008.06284.x. Epub 2008 Jun 28.
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Chromosomal toxin-antitoxin systems may act as antiaddiction modules.染色体毒素-抗毒素系统可能充当抗成瘾模块。
J Bacteriol. 2008 Jul;190(13):4603-9. doi: 10.1128/JB.00357-08. Epub 2008 Apr 25.
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The chemical genomic portrait of yeast: uncovering a phenotype for all genes.酵母的化学基因组图谱:揭示所有基因的表型
Science. 2008 Apr 18;320(5874):362-5. doi: 10.1126/science.1150021.
5
MazF, an mRNA interferase, mediates programmed cell death during multicellular Myxococcus development.MazF是一种mRNA干扰酶,在多细胞粘球菌发育过程中介导程序性细胞死亡。
Cell. 2008 Jan 11;132(1):55-66. doi: 10.1016/j.cell.2007.11.044.
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Folding of noncoding RNAs during transcription facilitated by pausing-induced nonnative structures.转录过程中非编码RNA的折叠由暂停诱导的非天然结构促进。
Proc Natl Acad Sci U S A. 2007 Nov 13;104(46):17995-8000. doi: 10.1073/pnas.0705038104. Epub 2007 Nov 6.
7
A linear pentapeptide is a quorum-sensing factor required for mazEF-mediated cell death in Escherichia coli.一种线性五肽是大肠杆菌中mazEF介导的细胞死亡所需的群体感应因子。
Science. 2007 Oct 26;318(5850):652-5. doi: 10.1126/science.1147248.
8
Proteomic identification of tmRNA substrates.tmRNA底物的蛋白质组学鉴定。
Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):17128-33. doi: 10.1073/pnas.0707671104. Epub 2007 Oct 15.
9
Structure probing of tmRNA in distinct stages of trans-translation.在反式翻译不同阶段对tmRNA进行结构探测。
RNA. 2007 May;13(5):713-22. doi: 10.1261/rna.451507. Epub 2007 Mar 30.
10
tmRNA determinants required for facilitating nonstop mRNA decay.促进无义mRNA降解所需的tmRNA决定因素。
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大肠杆菌K-12的tmRNA序列中对ACA三联体存在显著偏差。

Significant bias against the ACA triplet in the tmRNA sequence of Escherichia coli K-12.

作者信息

Baik Sarah, Inoue Koichi, Ouyang Ming, Inouye Masayori

机构信息

Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

出版信息

J Bacteriol. 2009 Oct;191(19):6157-66. doi: 10.1128/JB.00699-09. Epub 2009 Jul 24.

DOI:10.1128/JB.00699-09
PMID:19633073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2747887/
Abstract

The toxin MazF in Escherichia coli cleaves single-stranded RNAs specifically at ACA sequences. MazF overexpression virtually eliminates all cellular mRNAs to completely block protein synthesis. However, protein synthesis can continue on an mRNA that is devoid of ACA triplets. The finding that ribosomal RNAs remain intact in the face of complete translation arrest suggested a purpose for such preservation. We therefore examined the sequences of all transcribed RNAs to determine if there was any statistically significant bias against ACA. While ACA motifs are absent from tmRNA, 4.5S RNA, and seven of the eight 5S rRNAs, statistical analysis revealed that only for tmRNA was the absence nonrandom. The introduction of single-strand ACAs makes tmRNA highly susceptible to MazF cleavage. Furthermore, analysis of tmRNA sequences from 442 bacteria showed that the discrimination against ACA in tmRNAs was seen mostly in enterobacteria. We propose that the unusual bias against ACA in tmRNA may have coevolved with the acquisition of MazF.

摘要

大肠杆菌中的毒素MazF专门在ACA序列处切割单链RNA。MazF的过表达几乎消除了所有细胞mRNA,从而完全阻断蛋白质合成。然而,在没有ACA三联体的mRNA上,蛋白质合成仍可继续。核糖体RNA在完全翻译停滞的情况下仍保持完整这一发现表明了这种保留的目的。因此,我们检查了所有转录RNA的序列,以确定是否存在对ACA的任何统计学上显著的偏好。虽然在转移信使RNA(tmRNA)、4.5S RNA和八个5S核糖体RNA中的七个中不存在ACA基序,但统计分析表明,只有tmRNA的缺失是非随机的。单链ACA的引入使tmRNA极易受到MazF切割的影响。此外,对442种细菌的tmRNA序列分析表明,对tmRNA中ACA的歧视主要出现在肠杆菌中。我们提出,tmRNA中对ACA的异常偏好可能与MazF的获得共同进化。