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A c-di-GMP binding effector controls cell size in a cyanobacterium
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 evolut...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068817/ https://www.ncbi.nlm.nih.gov/pubmed/36947515 http://dx.doi.org/10.1073/pnas.2221874120 |
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author | Zeng, Xiaoli Huang, Min Sun, Qing-Xue Peng, Ye-Jun Xu, Xiaomei Tang, Yun-Bin Zhang, Ju-Yuan Yang, Yiling Zhang, Cheng-Cai |
author_facet | Zeng, Xiaoli Huang, Min Sun, Qing-Xue Peng, Ye-Jun Xu, Xiaomei Tang, Yun-Bin Zhang, Ju-Yuan Yang, Yiling Zhang, Cheng-Cai |
author_sort | Zeng, Xiaoli |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10068817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100688172023-09-22 A c-di-GMP binding effector controls cell size in a cyanobacterium Zeng, Xiaoli Huang, Min Sun, Qing-Xue Peng, Ye-Jun Xu, Xiaomei Tang, Yun-Bin Zhang, Ju-Yuan Yang, Yiling Zhang, Cheng-Cai Proc Natl Acad Sci U S A Biological Sciences 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. National Academy of Sciences 2023-03-22 2023-03-28 /pmc/articles/PMC10068817/ /pubmed/36947515 http://dx.doi.org/10.1073/pnas.2221874120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Zeng, Xiaoli Huang, Min Sun, Qing-Xue Peng, Ye-Jun Xu, Xiaomei Tang, Yun-Bin Zhang, Ju-Yuan Yang, Yiling Zhang, Cheng-Cai A c-di-GMP binding effector controls cell size in a cyanobacterium |
title | A c-di-GMP binding effector controls cell size in a cyanobacterium |
title_full | A c-di-GMP binding effector controls cell size in a cyanobacterium |
title_fullStr | A c-di-GMP binding effector controls cell size in a cyanobacterium |
title_full_unstemmed | A c-di-GMP binding effector controls cell size in a cyanobacterium |
title_short | A c-di-GMP binding effector controls cell size in a cyanobacterium |
title_sort | c-di-gmp binding effector controls cell size in a cyanobacterium |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068817/ https://www.ncbi.nlm.nih.gov/pubmed/36947515 http://dx.doi.org/10.1073/pnas.2221874120 |
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