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金属之战:调控 RNA 处于前沿

Battle for Metals: Regulatory RNAs at the Front Line.

机构信息

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, Strasbourg, France.

Department of Microbiology, University of Illinois Urbana-Champaign, Urbana IL, United States.

出版信息

Front Cell Infect Microbiol. 2022 Jul 5;12:952948. doi: 10.3389/fcimb.2022.952948. eCollection 2022.

Abstract

Metal such as iron, zinc, manganese, and nickel are essential elements for bacteria. These nutrients are required in crucial structural and catalytic roles in biological processes, including precursor biosynthesis, DNA replication, transcription, respiration, and oxidative stress responses. While essential, in excess these nutrients can also be toxic. The immune system leverages both of these facets, to limit bacterial proliferation and combat invaders. Metal binding immune proteins reduce the bioavailability of metals at the infection sites starving intruders, while immune cells intoxicate pathogens by providing metals in excess leading to enzyme mismetallation and/or reactive oxygen species generation. In this dynamic metal environment, maintaining metal homeostasis is a critical process that must be precisely coordinated. To achieve this, bacteria utilize diverse metal uptake and efflux systems controlled by metalloregulatory proteins. Recently, small regulatory RNAs (sRNAs) have been revealed to be critical post-transcriptional regulators, working in conjunction with transcription factors to promote rapid adaptation and to fine-tune bacterial adaptation to metal abundance. In this mini review, we discuss the expanding role for sRNAs in iron homeostasis, but also in orchestrating adaptation to the availability of other metals like manganese and nickel. Furthermore, we describe the sRNA-mediated interdependency between metal homeostasis and oxidative stress responses, and how regulatory networks controlled by sRNAs contribute to survival and virulence.

摘要

铁、锌、锰和镍等金属是细菌必需的元素。这些营养物质在生物过程中发挥着关键的结构和催化作用,包括前体生物合成、DNA 复制、转录、呼吸和氧化应激反应。虽然这些营养物质是必需的,但过量也可能有毒。免疫系统利用这两个方面来限制细菌的增殖和对抗入侵者。金属结合免疫蛋白减少感染部位金属的生物利用度,使入侵者饥饿,而免疫细胞通过过量提供金属导致酶错配位和/或活性氧的产生使病原体中毒。在这种动态的金属环境中,维持金属稳态是一个必须精确协调的关键过程。为了实现这一点,细菌利用多种金属摄取和外排系统,由金属调节蛋白控制。最近,小调控 RNA(sRNA)被揭示为关键的转录后调控因子,与转录因子一起促进快速适应,并微调细菌对金属丰度的适应。在这篇综述中,我们讨论了 sRNA 在铁稳态中的作用不断扩大,但也讨论了 sRNA 如何协调对其他金属(如锰和镍)的可用性的适应。此外,我们描述了 sRNA 介导的金属稳态和氧化应激反应之间的相互依存关系,以及 sRNA 控制的调控网络如何有助于生存和毒力。

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