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2
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3
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6
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7
Crystal structure of the catalytic domain of RluD, the only rRNA pseudouridine synthase required for normal growth of Escherichia coli.RluD催化结构域的晶体结构,RluD是大肠杆菌正常生长所需的唯一rRNA假尿嘧啶合酶。
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Suppression of DeltabipA phenotypes in Escherichia coli by abolishment of pseudouridylation at specific sites on the 23S rRNA.通过消除23S rRNA特定位点的假尿苷化来抑制大肠杆菌中的DeltabipA表型。
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Overexpressed L20 Rescues 50S Ribosomal Subunit Assembly Defects of -Deletion in .过表达的L20挽救了Δ-缺失在……中50S核糖体亚基组装缺陷。 (你提供的原文中部分内容不完整,可能影响更精准理解和翻译,比如“in.”后面应该还有具体信息)
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本文引用的文献

1
Ribosomal crystallography: initiation, peptide bond formation, and amino acid polymerization are hampered by antibiotics.核糖体晶体学:起始、肽键形成和氨基酸聚合受到抗生素的阻碍。
Annu Rev Microbiol. 2004;58:233-51. doi: 10.1146/annurev.micro.58.030603.123822.
2
Pseudouridylation at position 32 of mitochondrial and cytoplasmic tRNAs requires two distinct enzymes in Saccharomyces cerevisiae.在酿酒酵母中,线粒体和细胞质转运核糖核酸(tRNA)第32位的假尿苷化需要两种不同的酶。
J Biol Chem. 2004 Dec 17;279(51):52998-3006. doi: 10.1074/jbc.M409581200. Epub 2004 Oct 4.
3
Methylation of 23S rRNA nucleotide G745 is a secondary function of the RlmAI methyltransferase.23S核糖体RNA核苷酸G745的甲基化是RlmAI甲基转移酶的次要功能。
RNA. 2004 Nov;10(11):1713-20. doi: 10.1261/rna.7820104. Epub 2004 Sep 23.
4
Visualization of ribosome-recycling factor on the Escherichia coli 70S ribosome: functional implications.大肠杆菌70S核糖体上核糖体循环因子的可视化:功能意义
Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):8900-5. doi: 10.1073/pnas.0401904101. Epub 2004 Jun 3.
5
CsdA, a cold-shock RNA helicase from Escherichia coli, is involved in the biogenesis of 50S ribosomal subunit.CsdA是一种来自大肠杆菌的冷休克RNA解旋酶,参与50S核糖体亚基的生物合成。
Nucleic Acids Res. 2004 May 17;32(9):2751-9. doi: 10.1093/nar/gkh603. Print 2004.
6
Crystal structure of the catalytic domain of RluD, the only rRNA pseudouridine synthase required for normal growth of Escherichia coli.RluD催化结构域的晶体结构,RluD是大肠杆菌正常生长所需的唯一rRNA假尿嘧啶合酶。
RNA. 2004 Feb;10(2):231-9. doi: 10.1261/rna.5187404.
7
Authentic precursors to ribosomal subunits accumulate in Escherichia coli in the absence of functional DnaK chaperone.在缺乏功能性DnaK伴侣蛋白的情况下,核糖体亚基的真实前体在大肠杆菌中积累。
Mol Microbiol. 2004 Jan;51(1):189-201. doi: 10.1046/j.1365-2958.2003.03813.x.
8
Evaluation of the RNA determinants for bacterial and yeast RNase III binding and cleavage.细菌和酵母核糖核酸酶III结合与切割的RNA决定因素评估。
J Biol Chem. 2004 Jan 16;279(3):2231-41. doi: 10.1074/jbc.M309324200. Epub 2003 Oct 27.
9
The DEAD-box RNA helicase SrmB is involved in the assembly of 50S ribosomal subunits in Escherichia coli.DEAD盒RNA解旋酶SrmB参与大肠杆菌50S核糖体亚基的组装。
Mol Microbiol. 2003 Jun;48(5):1253-65. doi: 10.1046/j.1365-2958.2003.03513.x.
10
A novel unanticipated type of pseudouridine synthase with homologs in bacteria, archaea, and eukarya.一种新型的、意想不到的假尿苷合酶,在细菌、古细菌和真核生物中均有同源物。
RNA. 2003 Jun;9(6):711-21. doi: 10.1261/rna.5230603.

假尿苷合酶RluD是大肠杆菌正常核糖体组装和功能所必需的。

The pseudouridine synthase RluD is required for normal ribosome assembly and function in Escherichia coli.

作者信息

Gutgsell Nancy S, Deutscher Murray P, Ofengand James

机构信息

Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, Gautier Bldg., 1011 NW 15th St., Miami, FL 33136, USA.

出版信息

RNA. 2005 Jul;11(7):1141-52. doi: 10.1261/rna.2550105. Epub 2005 May 31.

DOI:10.1261/rna.2550105
PMID:15928344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1370798/
Abstract

RluD is the pseudouridine synthase responsible for the formation of Psi1911, Psi1915, and Psi1917 in Escherichia coli 23S rRNA. Previous work from our laboratory demonstrated that disruption of the rluD gene and/or loss of the pseudouridine residues for which it is responsible resulted in a severe growth phenotype. In the current work we have examined further the effect of the loss of the RluD protein and its product pseudouridine residues in a deletion strain lacking the rluD gene. This strain exhibits defects in ribosome assembly, biogenesis, and function. Specifically, there is a deficit of 70S ribosomes, an increase in 50S and 30S subunits, and the appearance of new 62S and 39S particles. Analysis of the 39S particles indicates that they are immature precursors of the 50S subunits, whereas the 62S particles are derived from the breakdown of unstable 70S ribosomes. In addition, purified mutant 70S ribosomes were found to be somewhat less efficient than wild type in protein synthesis. The defect in ribosome assembly and resulting growth phenotype of the mutant could be restored by expression of wild-type RluD and synthesis of Psi1911, Psi1915, and Psi1917 residues, but not by catalytically inactive mutant RluD proteins, incapable of pseudouridine formation. The data suggest that the loss of the pseudouridine residues can account for all aspects of the mutant phenotype; however, a possible second function of the RluD synthase is also discussed.

摘要

RluD是负责在大肠杆菌23S rRNA中形成假尿苷Psi1911、Psi1915和Psi1917的假尿苷合酶。我们实验室之前的工作表明,rluD基因的破坏和/或其负责的假尿苷残基的缺失会导致严重的生长表型。在当前的工作中,我们进一步研究了在缺乏rluD基因的缺失菌株中RluD蛋白及其产物假尿苷残基缺失的影响。该菌株在核糖体组装、生物合成和功能方面表现出缺陷。具体而言,70S核糖体数量不足,50S和30S亚基增加,并且出现了新的62S和39S颗粒。对39S颗粒的分析表明,它们是50S亚基的未成熟前体,而62S颗粒源自不稳定70S核糖体的分解。此外,发现纯化的突变型70S核糖体在蛋白质合成方面比野生型效率略低。通过表达野生型RluD以及合成Psi1911、Psi1915和Psi1917残基,可以恢复突变体在核糖体组装方面的缺陷以及由此产生的生长表型,但不能通过无催化活性、无法形成假尿苷的突变型RluD蛋白来恢复。数据表明,假尿苷残基的缺失可以解释突变体表型的所有方面;然而,也讨论了RluD合酶可能的第二种功能。