The conserved noncoding RNA ModT coordinates growth and virulence in Clostridioides difficile.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
Tina Lenče, Johannes Sulzer, Kilian Andress, Anne-Sophie Gribling-Burrer, Vanessa Lamm-Schmidt, Lars Barquist, Redmond P Smyth, Franziska Faber
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Abstract

Bacterial noncoding RNAs fulfill a variety of cellular functions as catalysts, as scaffolds in protein complexes or as regulators of gene expression. They often exhibit complex tertiary structures that are a key determinant of their biochemical function. Here, we characterize the structured "raiA motif" RNA from Clostridioides difficile, which is conserved in more than 2,500 bacterial species from the phyla Bacillota and Actinomycetota. We show that its transcript abundance and stability in exponentially growing bacteria rivals that of ribosomal RNAs. Deletion of the "raiA motif" RNA is associated with delayed transition into stationary phase, and changes in stationary phase pathways such as spore formation, hence we rename it ModT (modulator of transition phase). Mechanistically, we show that ModT-mediated changes in cellular cyclic di-GMP levels are linked to the pronounced sporulation defect in the modT mutant. Importantly, we show that expression profiles and isoform patterns of ModT are conserved in Clostridium perfringens and Paeniclostridium sordellii, and that these orthologs can functionally complement ModT in C. difficile. Chemical structure probing of ModT in vivo reveals dynamic refolding and provides initial evidence for a potential association of ModT with proteins. In summary, our findings indicate that ModT fulfills a conserved role in regulating growth transitions in bacteria and provide a crucial step towards delineating its molecular mechanism.

保守的非编码 RNA ModT 协调艰难梭菌的生长和毒力。
细菌非编码 RNA 具有多种细胞功能,如催化剂、蛋白质复合物支架或基因表达调节器。它们通常表现出复杂的三级结构,这是决定其生化功能的关键因素。在这里,我们描述了难辨梭状芽孢杆菌中结构化的 "raiA motif "RNA,它在芽孢杆菌科和放线菌科的 2500 多个细菌物种中是保守的。我们的研究表明,它在指数增长细菌中的转录本丰度和稳定性可与核糖体 RNA媲美。raiA motif "RNA的缺失与延迟过渡到静止期以及静止期途径(如孢子形成)的变化有关,因此我们将其命名为ModT(过渡阶段调节器)。从机理上讲,我们发现 ModT 介导的细胞环状二-GMP 水平变化与 modT 突变体明显的孢子形成缺陷有关。重要的是,我们发现 ModT 在产气荚膜梭菌(Clostridium perfringens)和梭状芽孢杆菌(Paeniclostridium sordellii)中的表达谱和异构体模式是保守的,而且这些直向同源物可以对艰难梭菌中的 ModT 进行功能互补。对体内 ModT 的化学结构探测显示了动态重折叠,并为 ModT 与蛋白质的潜在关联提供了初步证据。总之,我们的研究结果表明,ModT 在调控细菌的生长转换过程中发挥着保守的作用,并为阐明其分子机制迈出了关键的一步。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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