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Fitness advantages conferred by the L20-interacting RNA cis-regulator of ribosomal protein synthesis in Bacillus subtilis

机译:芽孢杆菌核糖体蛋白合成的L20相互作用的RNA顺式调节剂赋予健身优势

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In many bacteria, ribosomal proteins autogenously repress their own expression by interacting with RNA structures typically located in the 5'-UTRs of their mRNA transcripts. This regulation is necessary to maintain a balance between ribosomal proteins and rRNA to ensure proper ribosome production. Despite advances in noncoding RNA discovery and validation of RNA-protein regulatory interactions, the selective pressures that govern the formation and maintenance of such RNA cis-regulators in the context of an organism remain largely undetermined. To examine the impact disruptions to this regulation have on bacterial fitness, we introduced point mutations that abolish ribosomal protein binding and regulation into the RNA structure that controls expression of ribosomal proteins L20 and L35 within the Bacillus subtilis genome. Our studies indicate that removing this regulation results in reduced log phase growth, improper rRNA maturation, and the accumulation of a kinetically trapped or misassembled ribosomal particle at low temperatures, suggesting defects in ribosome synthesis. Such work emphasizes the important role regulatory RNAs play in the stoichiometric production of ribosomal components for proper ribosome composition and overall organism viability and reinforces the potential of targeting ribosomal protein production and ribosome assembly with novel antimicrobials.
机译:在许多细菌中,通过与通常位于其mRNA转录物的5'--UTRS中的RNA结构相互作用,核糖体蛋白通过与RNA结构相互作用而自体抑制它们的表达。该调节是在核糖体蛋白和RRNA之间保持平衡的必要条件,以确保适当的核糖体产生。尽管在非编码RNA发现和RNA蛋白调节相互作用的验证方面取得了进展,但在生物体的背景下,控制这些RNA顺式调节剂的形成和维持的选择性压力在很大程度上。为了检查该调节对细菌健身的影响中断,我们引入了将核糖体蛋白结合和调节中的点突变引入了控制核糖杆菌基因组内核糖体蛋白L20和L35的表达的RNA结构。我们的研究表明,去除该调节导致降低的日志相生长,不正确的rRNA成熟,以及在低温下的动力学捕获或遗传核糖体颗粒的积累,表明核糖体合成中的缺陷。这种工作强调了在核糖体组分的化学计量生产中起作用的重要作用,用于适当的核糖体组成和总体生物的活力,并加强靶向核糖体蛋白质产生和核糖体组装的潜力与新的抗微生物。

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