Subunit Composition of Ribosome in the yqgF Mutant Is Deficient in pre-16S rRNA Processing of Escherichia coli.

IF 1.2 Q2 Biochemistry, Genetics and Molecular Biology
Tatsuaki Kurata, Shinobu Nakanishi, Masayuki Hashimoto, Masato Taoka, Toshiaki Isobe, Jun-Ichi Kato
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引用次数: 3

Abstract

Escherichia coli 16S, 23S, and 5S ribosomal RNAs (rRNAs) are transcribed as a single primary transcript, which is subsequently processed into mature rRNAs by several RNases. Three RNases (RNase III, RNase E, and RNase G) were reported to function in processing the 5'-leader of precursor 16S rRNA (pre-16S rRNA). Previously, we showed that a novel essential YqgF is involved in that processing. Here we investigated the ribosome subunits of the yqgFts mutant by LC-MS/MS. The mutant ribosome had decreased copy numbers of ribosome protein S1, suggesting that the yqgF gene enables incorporation of ribosomal protein S1 into ribosome by processing of the 5'-end of pre-16S rRNA. The ribosome protein S1 is essential for translation in E. coli; therefore, our results suggest that YqgF converts the inactive form of newly synthesized ribosome into the active form at the final step of ribosome assembly.

yqgF突变体的核糖体亚基组成在大肠杆菌的前16s rRNA加工中存在缺陷。
大肠杆菌16S, 23S和5S核糖体rna (rrna)作为一个单一的初级转录物转录,随后由几个rnase加工成成熟的rrna。据报道,有三种RNase (RNase III、RNase E和RNase G)参与了前体16S rRNA (pre-16S rRNA)的5'-前导体的加工。在此之前,我们发现一种新的重要的YqgF参与了这一过程。本研究采用LC-MS/MS分析了yqgFts突变体的核糖体亚基。突变的核糖体减少了核糖体蛋白S1的拷贝数,这表明yqgF基因通过加工pre-16S rRNA的5'端使核糖体蛋白S1整合到核糖体中。在大肠杆菌中,核糖体蛋白S1是翻译所必需的;因此,我们的研究结果表明,YqgF在核糖体组装的最后一步将新合成的核糖体的无活性形式转化为活性形式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Microbiology and Biotechnology
Journal of Molecular Microbiology and Biotechnology 生物-生物工程与应用微生物
CiteScore
3.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: We are entering a new and exciting era of microbiological study and application. Recent advances in the now established disciplines of genomics, proteomics and bioinformatics, together with extensive cooperation between academic and industrial concerns have brought about an integration of basic and applied microbiology as never before.
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