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Subcellular localization of type IV pili regulates bacterial multicellular development

In mammals, subcellular protein localization of factors like planar cell polarity proteins is a key driver of the multicellular organization of tissues. Bacteria also form organized multicellular communities, but these patterns are largely thought to emerge from regulation of whole-cell processes li...

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Autores principales: Ellison, Courtney K., Fei, Chenyi, Dalia, Triana N., Wingreen, Ned S., Dalia, Ankur B., Shaevitz, Joshua W., Gitai, Zemer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596432/
https://www.ncbi.nlm.nih.gov/pubmed/36284096
http://dx.doi.org/10.1038/s41467-022-33564-7
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author Ellison, Courtney K.
Fei, Chenyi
Dalia, Triana N.
Wingreen, Ned S.
Dalia, Ankur B.
Shaevitz, Joshua W.
Gitai, Zemer
author_facet Ellison, Courtney K.
Fei, Chenyi
Dalia, Triana N.
Wingreen, Ned S.
Dalia, Ankur B.
Shaevitz, Joshua W.
Gitai, Zemer
author_sort Ellison, Courtney K.
collection PubMed
description In mammals, subcellular protein localization of factors like planar cell polarity proteins is a key driver of the multicellular organization of tissues. Bacteria also form organized multicellular communities, but these patterns are largely thought to emerge from regulation of whole-cell processes like growth, motility, cell shape, and differentiation. Here we show that a unique intracellular patterning of appendages known as type IV pili (T4P) can drive multicellular development of complex bacterial communities. Specifically, dynamic T4P appendages localize in a line along the long axis of the cell in the bacterium Acinetobacter baylyi. This long-axis localization is regulated by a functionally divergent chemosensory Pil-Chp system, and an atypical T4P protein homologue (FimV) bridges Pil-Chp signaling and T4P positioning. We further demonstrate through modeling and empirical approaches that subcellular T4P localization controls how individual cells interact with one another, independently of T4P dynamics, with different patterns of localization giving rise to distinct multicellular architectures. Our results reveal how subcellular patterning of single cells regulates the development of multicellular bacterial communities.
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spelling pubmed-95964322022-10-27 Subcellular localization of type IV pili regulates bacterial multicellular development Ellison, Courtney K. Fei, Chenyi Dalia, Triana N. Wingreen, Ned S. Dalia, Ankur B. Shaevitz, Joshua W. Gitai, Zemer Nat Commun Article In mammals, subcellular protein localization of factors like planar cell polarity proteins is a key driver of the multicellular organization of tissues. Bacteria also form organized multicellular communities, but these patterns are largely thought to emerge from regulation of whole-cell processes like growth, motility, cell shape, and differentiation. Here we show that a unique intracellular patterning of appendages known as type IV pili (T4P) can drive multicellular development of complex bacterial communities. Specifically, dynamic T4P appendages localize in a line along the long axis of the cell in the bacterium Acinetobacter baylyi. This long-axis localization is regulated by a functionally divergent chemosensory Pil-Chp system, and an atypical T4P protein homologue (FimV) bridges Pil-Chp signaling and T4P positioning. We further demonstrate through modeling and empirical approaches that subcellular T4P localization controls how individual cells interact with one another, independently of T4P dynamics, with different patterns of localization giving rise to distinct multicellular architectures. Our results reveal how subcellular patterning of single cells regulates the development of multicellular bacterial communities. Nature Publishing Group UK 2022-10-25 /pmc/articles/PMC9596432/ /pubmed/36284096 http://dx.doi.org/10.1038/s41467-022-33564-7 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
Ellison, Courtney K.
Fei, Chenyi
Dalia, Triana N.
Wingreen, Ned S.
Dalia, Ankur B.
Shaevitz, Joshua W.
Gitai, Zemer
Subcellular localization of type IV pili regulates bacterial multicellular development
title Subcellular localization of type IV pili regulates bacterial multicellular development
title_full Subcellular localization of type IV pili regulates bacterial multicellular development
title_fullStr Subcellular localization of type IV pili regulates bacterial multicellular development
title_full_unstemmed Subcellular localization of type IV pili regulates bacterial multicellular development
title_short Subcellular localization of type IV pili regulates bacterial multicellular development
title_sort subcellular localization of type iv pili regulates bacterial multicellular development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596432/
https://www.ncbi.nlm.nih.gov/pubmed/36284096
http://dx.doi.org/10.1038/s41467-022-33564-7
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