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第二信使信号分子环二腺苷酸驱动……中的发育周期进程。 (注:原文中“in”后面缺少具体内容)

The second messenger signaling molecule cyclic di-AMP drives developmental cycle progression in .

作者信息

Lee Junghoon, Ouellette Scot P

机构信息

Department of Pathology, Microbiology, and Immunology, College of Medicine, University of Nebraska Medical Center, Omaha, United States.

出版信息

Elife. 2025 Sep 10;14:RP104240. doi: 10.7554/eLife.104240.

Abstract

The obligate intracellular bacterium alternates between two functional forms during its developmental cycle: elementary body (EB) and reticulate body (RB). However, the molecular mechanisms governing the transitions between these forms are unknown. Here, we present evidence that cyclic di-AMP (c-di-AMP) is a key factor in triggering the transition from RB to EB (i.e., secondary differentiation) in the chlamydial developmental cycle. By overexpressing or knocking down expression of c-di-AMP synthase genes, we made strains producing different levels of c-di-AMP, which we linked to changes in secondary differentiation status. Increases in c-di-AMP resulted in an earlier increase in transcription of EB-associated genes, and this was further manifested in earlier production of EBs. In contrast, when c-di-AMP levels were decreased, developmental cycle progression was delayed. Based on these data, we conclude there is a threshold level of c-di-AMP needed to trigger secondary differentiation in . This study identifies a mechanism by which secondary differentiation is initiated in and reveals a critical role for the second messenger signaling molecule c-di-AMP in this process.

摘要

这种专性细胞内细菌在其发育周期中会在两种功能形式之间交替

原体(EB)和网状体(RB)。然而,控制这些形式之间转变的分子机制尚不清楚。在此,我们提供证据表明,环二腺苷酸(c-di-AMP)是衣原体发育周期中触发从RB向EB转变(即二次分化)的关键因素。通过过表达或敲低c-di-AMP合酶基因的表达,我们构建了产生不同水平c-di-AMP的菌株,并将其与二次分化状态的变化联系起来。c-di-AMP的增加导致EB相关基因转录提前增加,这进一步表现为EB的提前产生。相反,当c-di-AMP水平降低时,发育周期进程延迟。基于这些数据,我们得出结论,在[具体细菌名称未明确给出]中触发二次分化需要一定阈值水平的c-di-AMP。本研究确定了[具体细菌名称未明确给出]中启动二次分化的机制,并揭示了第二信使信号分子c-di-AMP在此过程中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/760c/12422730/44c8317f39b9/elife-104240-fig1.jpg

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