Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Xiaoli, Huang, Min, Sun, Qing-Xue, Peng, Ye-Jun, Xu, Xiaomei, Tang, Yun-Bin, Zhang, Ju-Yuan, Yang, Yiling, Zhang, Cheng-Cai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
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
_version_ 1785018743593631744
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
work_keys_str_mv AT zengxiaoli acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT huangmin acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT sunqingxue acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT pengyejun acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT xuxiaomei acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT tangyunbin acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT zhangjuyuan acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT yangyiling acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT zhangchengcai acdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT zengxiaoli cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT huangmin cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT sunqingxue cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT pengyejun cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT xuxiaomei cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT tangyunbin cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT zhangjuyuan cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT yangyiling cdigmpbindingeffectorcontrolscellsizeinacyanobacterium
AT zhangchengcai cdigmpbindingeffectorcontrolscellsizeinacyanobacterium