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Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub

Asymmetric cell division (ACD) produces morphologically and behaviorally distinct cells and is the primary way to generate cell diversity. In the model bacterium Caulobacter crescentus, the polarization of distinct scaffold-signaling hubs at the swarmer and stalked cell poles constitutes the basis o...

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Autores principales: Tan, Wei, Cheng, Sihua, Li, Yingying, Li, Xiao-Yang, Lu, Ning, Sun, Jingxian, Tang, Guiyue, Yang, Yujiao, Cai, Kezhu, Li, Xuefei, Ou, Xijun, Gao, Xiang, Zhao, Guo-Ping, Childers, W. Seth, Zhao, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684454/
https://www.ncbi.nlm.nih.gov/pubmed/36418326
http://dx.doi.org/10.1038/s41467-022-35000-2
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author Tan, Wei
Cheng, Sihua
Li, Yingying
Li, Xiao-Yang
Lu, Ning
Sun, Jingxian
Tang, Guiyue
Yang, Yujiao
Cai, Kezhu
Li, Xuefei
Ou, Xijun
Gao, Xiang
Zhao, Guo-Ping
Childers, W. Seth
Zhao, Wei
author_facet Tan, Wei
Cheng, Sihua
Li, Yingying
Li, Xiao-Yang
Lu, Ning
Sun, Jingxian
Tang, Guiyue
Yang, Yujiao
Cai, Kezhu
Li, Xuefei
Ou, Xijun
Gao, Xiang
Zhao, Guo-Ping
Childers, W. Seth
Zhao, Wei
author_sort Tan, Wei
collection PubMed
description Asymmetric cell division (ACD) produces morphologically and behaviorally distinct cells and is the primary way to generate cell diversity. In the model bacterium Caulobacter crescentus, the polarization of distinct scaffold-signaling hubs at the swarmer and stalked cell poles constitutes the basis of ACD. However, mechanisms involved in the formation of these hubs remain elusive. Here, we show that a swarmer-cell-pole scaffold, PodJ, forms biomolecular condensates both in vitro and in living cells via phase separation. The coiled-coil 4–6 and the intrinsically disordered regions are the primary domains that contribute to biomolecular condensate generation and signaling protein recruitment in PodJ. Moreover, a negative regulation of PodJ phase separation by the stalked-cell-pole scaffold protein SpmX is revealed. SpmX impedes PodJ cell-pole accumulation and affects its recruitment ability. Together, by modulating the assembly and dynamics of scaffold-signaling hubs, phase separation may serve as a general biophysical mechanism that underlies the regulation of ACD in bacteria and other organisms.
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spelling pubmed-96844542022-11-25 Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub Tan, Wei Cheng, Sihua Li, Yingying Li, Xiao-Yang Lu, Ning Sun, Jingxian Tang, Guiyue Yang, Yujiao Cai, Kezhu Li, Xuefei Ou, Xijun Gao, Xiang Zhao, Guo-Ping Childers, W. Seth Zhao, Wei Nat Commun Article Asymmetric cell division (ACD) produces morphologically and behaviorally distinct cells and is the primary way to generate cell diversity. In the model bacterium Caulobacter crescentus, the polarization of distinct scaffold-signaling hubs at the swarmer and stalked cell poles constitutes the basis of ACD. However, mechanisms involved in the formation of these hubs remain elusive. Here, we show that a swarmer-cell-pole scaffold, PodJ, forms biomolecular condensates both in vitro and in living cells via phase separation. The coiled-coil 4–6 and the intrinsically disordered regions are the primary domains that contribute to biomolecular condensate generation and signaling protein recruitment in PodJ. Moreover, a negative regulation of PodJ phase separation by the stalked-cell-pole scaffold protein SpmX is revealed. SpmX impedes PodJ cell-pole accumulation and affects its recruitment ability. Together, by modulating the assembly and dynamics of scaffold-signaling hubs, phase separation may serve as a general biophysical mechanism that underlies the regulation of ACD in bacteria and other organisms. Nature Publishing Group UK 2022-11-23 /pmc/articles/PMC9684454/ /pubmed/36418326 http://dx.doi.org/10.1038/s41467-022-35000-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tan, Wei
Cheng, Sihua
Li, Yingying
Li, Xiao-Yang
Lu, Ning
Sun, Jingxian
Tang, Guiyue
Yang, Yujiao
Cai, Kezhu
Li, Xuefei
Ou, Xijun
Gao, Xiang
Zhao, Guo-Ping
Childers, W. Seth
Zhao, Wei
Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title_full Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title_fullStr Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title_full_unstemmed Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title_short Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
title_sort phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684454/
https://www.ncbi.nlm.nih.gov/pubmed/36418326
http://dx.doi.org/10.1038/s41467-022-35000-2
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