Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada.
Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada.
Appl Environ Microbiol. 2023 Apr 26;89(4):e0001523. doi: 10.1128/aem.00015-23. Epub 2023 Mar 15.
Compartmentalization of macromolecules into discrete non-lipid-bound bodies by liquid-liquid phase separation (LLPS) is a well-characterized regulatory mechanism frequently associated with the cellular stress response in eukaryotes. In contrast, the formation and importance of similar complexes is just becoming evident in bacteria. Here, we identify LLPS as the mechanism by which the DEAD-box RNA helicase, cyanobacterial RNA helicase redox (CrhR), compartmentalizes into dynamic membraneless organelles in a temporal and spatial manner in response to abiotic stress in the cyanobacterium sp. strain PCC 6803. Stress conditions induced CrhR to form a single crescent localized exterior to the thylakoid membrane, indicating that this region is a crucial domain in the cyanobacterial stress response. These crescents rapidly dissipate upon alleviation of the stress conditions. Furthermore, CrhR aggregation was mediated by LLPS in an RNA-dependent reaction. We propose that dynamic CrhR condensation performs crucial roles in RNA metabolism, enabling rapid adaptation of the photosynthetic apparatus to environmental stresses. These results expand our understanding of the role that functional compartmentalization of RNA helicases and thus RNA processing in membraneless organelles by LLPS-mediated protein condensation performs in the bacterial response to environmental stress. Oxygen-evolving photosynthetic cyanobacteria evolved ~3 billion years ago, performing fundamental roles in the biogeochemical evolution of the early Earth and continue to perform fundamental roles in nutrient cycling and primary productivity today. The phylum consists of diverse species that flourish in heterogeneous environments. A prime driver for survival is the ability to alter photosynthetic performance in response to the shifting environmental conditions these organisms continuously encounter. This study demonstrated that diverse abiotic stresses elicit dramatic changes in localization and structural organization of the RNA helicase CrhR associated with the photosynthetic thylakoid membrane. These dynamic changes, mediated by a liquid-liquid phase separation (LLPS)-mediated mechanism, reveal a novel mechanism by which cyanobacteria can compartmentalize the activity of ribonucleoprotein complexes in membraneless organelles. The results have significant consequences for understanding bacterial adaptation and survival in response to changing environmental conditions.
通过液-液相分离(LLPS)将大分子分隔成离散的非脂结合体是一种特征明确的调控机制,经常与真核生物的细胞应激反应相关。相比之下,类似复合物的形成和重要性在细菌中才刚刚显现出来。在这里,我们发现 DEAD-box RNA 解旋酶,蓝细菌 RNA 解旋酶氧化还原(CrhR),通过 LLPS 机制以时间和空间的方式分隔成动态无膜细胞器,以响应蓝藻 sp. PCC 6803 中的非生物胁迫。胁迫条件诱导 CrhR 形成一个位于类囊体膜外部的新月形,表明该区域是蓝细菌应激反应的关键结构域。这些新月形在胁迫条件缓解后迅速消失。此外,CrhR 聚集是通过 LLPS 介导的 RNA 依赖性反应介导的。我们提出,动态 CrhR 凝聚在 RNA 代谢中发挥关键作用,使光合作用装置能够快速适应环境胁迫。这些结果扩展了我们对 RNA 解旋酶的功能分隔以及通过 LLPS 介导的蛋白质凝聚在无膜细胞器中进行的 RNA 加工在细菌对环境胁迫的反应中的作用的理解。 产氧光合蓝细菌大约在 30 亿年前进化而来,在地球早期的生物地球化学进化中发挥着重要作用,今天仍在营养循环和初级生产力中发挥着重要作用。该门由多种在异质环境中茁壮成长的物种组成。生存的主要驱动力是改变光合作用性能以适应生物体不断遇到的不断变化的环境条件的能力。这项研究表明,各种非生物胁迫会引起与光合类囊体膜相关的 RNA 解旋酶 CrhR 的定位和结构组织发生剧烈变化。这些动态变化由液-液相分离(LLPS)介导的机制介导,揭示了蓝细菌可以在无膜细胞器中分隔核糖核蛋白复合物活性的新机制。这些结果对理解细菌适应和生存有重要意义响应不断变化的环境条件。