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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
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.
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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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