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YebU是一种特异性作用于16 S rRNA核苷酸1407的m5C甲基转移酶。

YebU is a m5C methyltransferase specific for 16 S rRNA nucleotide 1407.

作者信息

Andersen Niels Møller, Douthwaite Stephen

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, DK-5230 Odense M, Denmark.

出版信息

J Mol Biol. 2006 Jun 9;359(3):777-86. doi: 10.1016/j.jmb.2006.04.007. Epub 2006 Apr 21.

Abstract

The rRNAs in Escherichia coli contain methylations at 24 nucleotides, which collectively are important for ribosome function. Three of these methylations are m5C modifications located at nucleotides C967 and C1407 in 16S rRNA and at nucleotide C1962 in 23S rRNA. Bacterial rRNA modifications generally require specific enzymes, and only one m5C rRNA methyltransferase, RsmB (formerly Fmu) that methylates nucleotide C967, has previously been identified. BLAST searches of the E.coli genome revealed a single gene, yebU, with sufficient similarity to rsmB to encode a putative m5C RNA methyltransferase. This suggested that the yebU gene product modifies C1407 and/or C1962. Here, we analysed the E.coli rRNAs by matrix assisted laser desorption/ionization mass spectrometry and show that inactivation of the yebU gene leads to loss of methylation at C1407 in 16 S rRNA, but does not interfere with methylation at C1962 in 23 S rRNA. Purified recombinant YebU protein retains its specificity for C1407 in vitro, and methylates 30 S subunits (but not naked 16 S rRNA or 70 S ribosomes) isolated from yebU knockout strains. Nucleotide C1407 is located at a functionally active region of the 30 S subunit interface close to the P site, and YebU-directed methylation of this nucleotide seems to be conserved in bacteria. The yebU knockout strains display slower growth and reduced fitness in competition with wild-type cells. We suggest that a more appropriate designation for yebU would be the rRNA small subunit methyltransferase gene rsmF, and that the nomenclature system be extended to include the rRNA methyltransferases that still await identification.

摘要

大肠杆菌中的核糖体RNA(rRNA)在24个核苷酸处含有甲基化修饰,这些修饰共同对核糖体功能至关重要。其中三种甲基化修饰是5-甲基胞嘧啶(m5C)修饰,分别位于16S rRNA的核苷酸C967和C1407以及23S rRNA的核苷酸C1962处。细菌rRNA修饰通常需要特定的酶,此前仅鉴定出一种能使核苷酸C967发生甲基化的m5C rRNA甲基转移酶RsmB(以前称为Fmu)。对大肠杆菌基因组进行的BLAST搜索揭示了一个单一基因yebU,它与rsmB具有足够的相似性,可编码一种假定的m5C RNA甲基转移酶。这表明yebU基因产物可修饰C1407和/或C1962。在此,我们通过基质辅助激光解吸/电离质谱法分析了大肠杆菌的rRNA,结果表明yebU基因失活会导致16S rRNA中C1407处的甲基化缺失,但不影响23S rRNA中C1962处的甲基化。纯化的重组YebU蛋白在体外对C1407仍保持其特异性,并能使从yebU基因敲除菌株中分离出的30S亚基(但不是裸露的16S rRNA或70S核糖体)发生甲基化。核苷酸C1407位于30S亚基界面靠近P位点的功能活性区域,这种核苷酸的YebU介导的甲基化在细菌中似乎是保守的。yebU基因敲除菌株在与野生型细胞竞争时生长较慢且适应性降低。我们建议将yebU更合适地命名为rRNA小亚基甲基转移酶基因rsmF,并扩展命名系统以包括尚未鉴定的rRNA甲基转移酶。

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