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Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX
Filamentous actinobacteria such as Streptomyces undergo two distinct modes of cell division, leading to partitioning of growing hyphae into multicellular compartments via cross-walls, and to septation and release of unicellular spores. Specific determinants for cross-wall formation and the importanc...
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/PMC8748795/ https://www.ncbi.nlm.nih.gov/pubmed/35013186 http://dx.doi.org/10.1038/s41467-021-27638-1 |
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author | Bush, Matthew J. Gallagher, Kelley A. Chandra, Govind Findlay, Kim C. Schlimpert, Susan |
author_facet | Bush, Matthew J. Gallagher, Kelley A. Chandra, Govind Findlay, Kim C. Schlimpert, Susan |
author_sort | Bush, Matthew J. |
collection | PubMed |
description | Filamentous actinobacteria such as Streptomyces undergo two distinct modes of cell division, leading to partitioning of growing hyphae into multicellular compartments via cross-walls, and to septation and release of unicellular spores. Specific determinants for cross-wall formation and the importance of hyphal compartmentalization for Streptomyces development are largely unknown. Here we show that SepX, an actinobacterial-specific protein, is crucial for both cell division modes in Streptomyces venezuelae. Importantly, we find that sepX-deficient mutants grow without cross-walls and that this substantially impairs the fitness of colonies and the coordinated progression through the developmental life cycle. Protein interaction studies and live-cell imaging suggest that SepX contributes to the stabilization of the divisome, a mechanism that also requires the dynamin-like protein DynB. Thus, our work identifies an important determinant for cell division in Streptomyces that is required for cellular development and sporulation. |
format | Online Article Text |
id | pubmed-8748795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87487952022-01-20 Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX Bush, Matthew J. Gallagher, Kelley A. Chandra, Govind Findlay, Kim C. Schlimpert, Susan Nat Commun Article Filamentous actinobacteria such as Streptomyces undergo two distinct modes of cell division, leading to partitioning of growing hyphae into multicellular compartments via cross-walls, and to septation and release of unicellular spores. Specific determinants for cross-wall formation and the importance of hyphal compartmentalization for Streptomyces development are largely unknown. Here we show that SepX, an actinobacterial-specific protein, is crucial for both cell division modes in Streptomyces venezuelae. Importantly, we find that sepX-deficient mutants grow without cross-walls and that this substantially impairs the fitness of colonies and the coordinated progression through the developmental life cycle. Protein interaction studies and live-cell imaging suggest that SepX contributes to the stabilization of the divisome, a mechanism that also requires the dynamin-like protein DynB. Thus, our work identifies an important determinant for cell division in Streptomyces that is required for cellular development and sporulation. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748795/ /pubmed/35013186 http://dx.doi.org/10.1038/s41467-021-27638-1 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 Bush, Matthew J. Gallagher, Kelley A. Chandra, Govind Findlay, Kim C. Schlimpert, Susan Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title | Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title_full | Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title_fullStr | Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title_full_unstemmed | Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title_short | Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX |
title_sort | hyphal compartmentalization and sporulation in streptomyces require the conserved cell division protein sepx |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748795/ https://www.ncbi.nlm.nih.gov/pubmed/35013186 http://dx.doi.org/10.1038/s41467-021-27638-1 |
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