Involvement of Escherichia coli YbeX/CorC in ribosomal metabolism.

IF 2.6 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Microbiology Pub Date : 2024-05-01 Epub Date: 2024-03-17 DOI:10.1111/mmi.15248
İsmail Sarıgül, Amata Žukova, Emel Alparslan, Sille Remm, Margus Pihlak, Niilo Kaldalu, Tanel Tenson, Ülo Maiväli
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Abstract

YbeX of Escherichia coli, a member of the CorC protein family, is encoded in the same operon with ribosome-associated proteins YbeY and YbeZ. Here, we report the involvement of YbeX in ribosomal metabolism. The ΔybeX cells accumulate distinct 16S rRNA degradation intermediates in the 30S particles and the 70S ribosomes. E. coli lacking ybeX has a lengthened lag phase upon outgrowth from the stationary phase. This growth phenotype is heterogeneous at the individual cell level and especially prominent under low extracellular magnesium levels. The ΔybeX strain is sensitive to elevated growth temperatures and to several ribosome-targeting antibiotics that have in common the ability to induce the cold shock response in E. coli. Although generally milder, the phenotypes of the ΔybeX mutant overlap with those caused by ybeY deletion. A genetic screen revealed partial compensation of the ΔybeX growth phenotype by the overexpression of YbeY. These findings indicate an interconnectedness among the ybeZYX operon genes, highlighting their roles in ribosomal assembly and/or degradation.

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大肠杆菌 YbeX/CorC 参与核糖体代谢的情况
大肠杆菌的 YbeX 是 CorC 蛋白家族的成员,与核糖体相关蛋白 YbeY 和 YbeZ 编码在同一个操作子中。在这里,我们报告了 YbeX 参与核糖体代谢的情况。ΔybeX 细胞在 30S 颗粒和 70S 核糖体中积累了不同的 16S rRNA 降解中间产物。缺乏 ybeX 的大肠杆菌从静止期生长出来后,滞后期延长。这种生长表型在单个细胞水平上具有异质性,在细胞外镁含量较低的情况下尤为突出。ΔybeX 菌株对升高的生长温度和几种核糖体靶向抗生素敏感,这些抗生素的共同点是能够诱导大肠杆菌的冷休克反应。ΔybeX突变体的表型虽然一般较温和,但与ybeY缺失造成的表型重叠。基因筛选发现,YbeY的过表达可部分补偿ΔybeX的生长表型。这些发现表明 ybeZYX 操作子基因之间存在着相互联系,突出了它们在核糖体组装和/或降解中的作用。
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来源期刊
Molecular Microbiology
Molecular Microbiology 生物-生化与分子生物学
CiteScore
7.20
自引率
5.60%
发文量
132
审稿时长
1.7 months
期刊介绍: Molecular Microbiology, the leading primary journal in the microbial sciences, publishes molecular studies of Bacteria, Archaea, eukaryotic microorganisms, and their viruses. Research papers should lead to a deeper understanding of the molecular principles underlying basic physiological processes or mechanisms. Appropriate topics include gene expression and regulation, pathogenicity and virulence, physiology and metabolism, synthesis of macromolecules (proteins, nucleic acids, lipids, polysaccharides, etc), cell biology and subcellular organization, membrane biogenesis and function, traffic and transport, cell-cell communication and signalling pathways, evolution and gene transfer. Articles focused on host responses (cellular or immunological) to pathogens or on microbial ecology should be directed to our sister journals Cellular Microbiology and Environmental Microbiology, respectively.
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