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EzrA通过其QNR基序与FtsA的相互作用促进Z环的形成。

EzrA promotes Z-ring formation through interaction of its QNR motif with FtsA.

作者信息

Li Tingting, Liu Xiujian, Zhang Liangsheng, Li Haotian, Ni Minghui, Zou Wenjin, Liang Menglei, Gong Ruotong, Hu Qiao, Zhao Lelin, Hu Zhe, Li Lu, Huang Qi, Zhou Rui

机构信息

State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

Institute of Animal Husbandry and Veterinary, Hubei Academy of Agricultural Sciences, Wuhan, China.

出版信息

J Bacteriol. 2025 Jul 24;207(7):e0012525. doi: 10.1128/jb.00125-25. Epub 2025 Jul 3.

Abstract

Bacterial cell division requires precise placement and formation of the division machinery to ensure the accurate generation of identical daughter cells. This process is canonically initiated by the highly conserved FtsZ but also needs the involvement of a variety of FtsZ-binding proteins to orchestrate the spatial and temporal positioning and assembly of the Z-ring. However, the underlying molecular mechanisms remain poorly understood. In this study, we characterized the roles of an important FtsZ binding protein EzrA in the cell division of , an emerging zoonotic bacterial pathogen. Our results revealed that EzrA shares high subcellular dynamics with FtsZ during the entire cell division cycle and functions primarily as a positive regulator for Z-ring formation. Co-immunoprecipitation and bacterial two-hybrid data suggest that EzrA interacts with FtsZ and several early division proteins. Importantly, the conserved QNR motif in EzrA directly contributes to its interaction with FtsA. Disrupting this motif results in the mislocalization of EzrA itself at the division site rather than the localization of FtsA, which remains concentrated localization at the division site. Moreover, the interaction of EzrA through the QNR motif with FtsA is conserved among the . Taken together, these findings demonstrate EzrA as a regulator of Z-ring positioning to the division site through the interaction of its conserved QNR motif with FtsA.IMPORTANCEBacteria replicate through binary fission in which the FtsZ-ring positioning and assembly is a crucial process requiring precise spatial and temporal regulation. However, the mechanism of this process remains largely unknown, especially in ovoid-shaped bacteria, such as in which many members are important human and animal pathogens. In this study, we characterize the critical role of the cell division regulator EzrA in the formation of the Z-ring. Our data reveal a model in which EzrA interacts through its QNR motif with FtsA to be properly localized to the septum so as to facilitate the positioning and formation of the Z-ring of . This regulatory mechanism could be conserved in . This research provides insights into the regulation mechanism of the Z-ring formation and will contribute to the understanding of the cell division process in .

摘要

细菌细胞分裂需要精确放置和形成分裂机器,以确保准确产生相同的子细胞。这一过程通常由高度保守的FtsZ启动,但也需要多种FtsZ结合蛋白的参与,以协调Z环的时空定位和组装。然而,其潜在的分子机制仍知之甚少。在本研究中,我们表征了一种重要的FtsZ结合蛋白EzrA在一种新出现的人畜共患病细菌病原体的细胞分裂中的作用。我们的结果表明,EzrA在整个细胞分裂周期中与FtsZ具有高度的亚细胞动态,并且主要作为Z环形成的正调节因子发挥作用。免疫共沉淀和细菌双杂交数据表明,EzrA与FtsZ和几种早期分裂蛋白相互作用。重要的是,EzrA中保守的QNR基序直接促成其与FtsA的相互作用。破坏这个基序会导致EzrA自身在分裂位点的错误定位,而不是FtsA的定位,FtsA仍集中定位在分裂位点。此外,EzrA通过QNR基序与FtsA的相互作用在中是保守的。综上所述,这些发现表明EzrA通过其保守的QNR基序与FtsA的相互作用,作为Z环定位到分裂位点的调节因子。重要性细菌通过二分裂进行复制,其中FtsZ环的定位和组装是一个关键过程,需要精确的时空调节。然而,这一过程的机制在很大程度上仍然未知,特别是在卵形细菌中,例如许多成员是重要的人类和动物病原体。在本研究中,我们表征了细胞分裂调节因子EzrA在Z环形成中的关键作用。我们的数据揭示了一个模型,其中EzrA通过其QNR基序与FtsA相互作用,从而正确定位到隔膜,以促进的Z环的定位和形成。这种调节机制可能在中是保守的。这项研究为Z环形成的调节机制提供了见解,并将有助于理解中的细胞分裂过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/12288466/c71425ab4ae1/jb.00125-25.f001.jpg

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