A c-di-GMP binding effector controls cell size in a cyanobacterium.
A c-di-GMP binding effector controls cell size in a cyanobacterium.
复制标题
DOI:
10.1073/pnas.2221874120
复制
发表时间:
2023-03-28
影响因子:
11.1
通讯作者:
Zhang, Cheng-Cai
中科院分区:
文献类型:
--
作者:
Zeng, Xiaoli;Huang, Min;Sun, Qing-Xue;Peng, Ye-Jun;Xu, Xiaomei;Tang, Yun-Bin;Zhang, Ju-Yuan;Yang, Yiling;Zhang, Cheng-Cai
Cell size homeostasis is an essential physical trait of bacteria, and how the cell size is maintained and regulated remains an important question in microbiology. We recently found that the second messenger c-di-GMP may be an intracellular proxy for cell size control in Anabaena. In this study, we identified and characterized a highly conserved c-di-GMP receptor in cyanobacteria and demonstrated that it regulates cell size via interaction with the transcription factor DevH in Anabaena. These findings not only provide a mechanism of cell size regulation but also extend the role of c-di-GMP receptors in bacteria. Since c-di-GMP plays broad functions in cyanobacteria, our pioneering study constitutes a basis for studies on c-di-GMP signaling in these organisms. Cyclic-di-GMP (c-di-GMP) is a ubiquitous bacterial signaling molecule. It is also a critical player in the regulation of cell size and cell behaviors such as cell aggregation and phototaxis in cyanobacteria, which constitute an important group of prokaryotes for their roles in the ecology and evolution of the Earth. However, c-di-GMP receptors have never been revealed in cyanobacteria. Here, we report the identification of a c-di-GMP receptor, CdgR, from the filamentous cyanobacterium Anabaena PCC 7120. Crystal structural analysis and genetic studies demonstrate that CdgR binds c-di-GMP at the dimer interface and this binding is required for the control of cell size in a c-di-GMP-dependent manner. Different functions of CdgR, in ligand binding and signal transmission, could be separated genetically, allowing us to dissect its molecular signaling functions. The presence of the apo-form of CdgR triggers cell size reduction, consistent with the similar effects observed with a decrease of c-di-GMP levels in cells. Furthermore, we found that CdgR exerts its function by interacting with a global transcription factor DevH, and this interaction was inhibited by c-di-GMP. The lethal effect triggered by conditional depletion of DevH or by the production of several point-mutant proteins of CdgR in cells indicates that this signaling pathway plays critical functions in Anabaena. Our studies revealed a mechanism of c-di-GMP signaling in the control of cell size, an important and complex trait for bacteria. CdgR is highly conserved in cyanobacteria, which will greatly expand our understanding of the roles of c-di-GMP signaling in these organisms.
登录
查看更多内容
影响因子:
5.2
作者:
Huang M;Zhang JY;Zeng X;Zhang CC
通讯作者:
Zhang CC
DOI:
10.1107/s0907444904019158
发表时间:
2004-12-01
影响因子:
2.2
作者:
Emsley, P;Cowtan, K
通讯作者:
Cowtan, K
DOI:
10.1107/s0907444909052925
发表时间:
2010-02
期刊:
Acta crystallographica. Section D, Biological crystallography
影响因子:
--
作者:
Adams PD;Afonine PV;Bunkóczi G;Chen VB;Davis IW;Echols N;Headd JJ;Hung LW;Kapral GJ;Grosse-Kunstleve RW;McCoy AJ;Moriarty NW;Oeffner R;Read RJ;Richardson DC;Richardson JS;Terwilliger TC;Zwart PH
通讯作者:
Zwart PH
影响因子:
4.7
作者:
Niu, Tian-Cai;Lin, Gui-Ming;Zhang, Cheng-Cai
通讯作者:
Zhang, Cheng-Cai
影响因子:
7.3
作者:
Hengge, Regine
通讯作者:
Hengge, Regine