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Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus
Cell polarity development is the prerequisite for cell differentiation and generating biodiversity. In the model bacterium Caulobacter crescentus, the polarization of the scaffold protein PopZ during the predivisional cell stage plays a central role in asymmetric cell division. However, our understa...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127582/ https://www.ncbi.nlm.nih.gov/pubmed/36971555 http://dx.doi.org/10.1128/mbio.03218-22 |
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author | Lu, Ning Duvall, Samuel W. Zhao, Guohong Kowallis, Kimberley A. Zhang, Chao Tan, Wei Sun, Jingxian Petitjean, Haley N. Tomares, Dylan T. Zhao, Guo-Ping Childers, W. Seth Zhao, Wei |
author_facet | Lu, Ning Duvall, Samuel W. Zhao, Guohong Kowallis, Kimberley A. Zhang, Chao Tan, Wei Sun, Jingxian Petitjean, Haley N. Tomares, Dylan T. Zhao, Guo-Ping Childers, W. Seth Zhao, Wei |
author_sort | Lu, Ning |
collection | PubMed |
description | Cell polarity development is the prerequisite for cell differentiation and generating biodiversity. In the model bacterium Caulobacter crescentus, the polarization of the scaffold protein PopZ during the predivisional cell stage plays a central role in asymmetric cell division. However, our understanding of the spatiotemporal regulation of PopZ localization remains incomplete. In the current study, a direct interaction between PopZ and the new pole scaffold PodJ is revealed, which plays a primary role in triggering the new pole accumulation of PopZ. The coiled-coil 4-6 domain in PodJ is responsible for interacting with PopZ in vitro and promoting PopZ transition from monopolar to bipolar in vivo. Elimination of the PodJ-PopZ interaction impairs the PopZ-mediated chromosome segregation by affecting both the positioning and partitioning of the ParB-parS centromere. Further analyses of PodJ and PopZ from other bacterial species indicate this scaffold-scaffold interaction may represent a widespread strategy for spatiotemporal regulation of cell polarity in bacteria. |
format | Online Article Text |
id | pubmed-10127582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101275822023-04-26 Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus Lu, Ning Duvall, Samuel W. Zhao, Guohong Kowallis, Kimberley A. Zhang, Chao Tan, Wei Sun, Jingxian Petitjean, Haley N. Tomares, Dylan T. Zhao, Guo-Ping Childers, W. Seth Zhao, Wei mBio Research Article Cell polarity development is the prerequisite for cell differentiation and generating biodiversity. In the model bacterium Caulobacter crescentus, the polarization of the scaffold protein PopZ during the predivisional cell stage plays a central role in asymmetric cell division. However, our understanding of the spatiotemporal regulation of PopZ localization remains incomplete. In the current study, a direct interaction between PopZ and the new pole scaffold PodJ is revealed, which plays a primary role in triggering the new pole accumulation of PopZ. The coiled-coil 4-6 domain in PodJ is responsible for interacting with PopZ in vitro and promoting PopZ transition from monopolar to bipolar in vivo. Elimination of the PodJ-PopZ interaction impairs the PopZ-mediated chromosome segregation by affecting both the positioning and partitioning of the ParB-parS centromere. Further analyses of PodJ and PopZ from other bacterial species indicate this scaffold-scaffold interaction may represent a widespread strategy for spatiotemporal regulation of cell polarity in bacteria. American Society for Microbiology 2023-03-27 /pmc/articles/PMC10127582/ /pubmed/36971555 http://dx.doi.org/10.1128/mbio.03218-22 Text en Copyright © 2023 Lu et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Lu, Ning Duvall, Samuel W. Zhao, Guohong Kowallis, Kimberley A. Zhang, Chao Tan, Wei Sun, Jingxian Petitjean, Haley N. Tomares, Dylan T. Zhao, Guo-Ping Childers, W. Seth Zhao, Wei Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title | Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title_full | Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title_fullStr | Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title_full_unstemmed | Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title_short | Scaffold-Scaffold Interaction Facilitates Cell Polarity Development in Caulobacter crescentus |
title_sort | scaffold-scaffold interaction facilitates cell polarity development in caulobacter crescentus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127582/ https://www.ncbi.nlm.nih.gov/pubmed/36971555 http://dx.doi.org/10.1128/mbio.03218-22 |
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