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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9684454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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