Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bush, Matthew J., Gallagher, Kelley A., Chandra, Govind, Findlay, Kim C., Schlimpert, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784631084943671296
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
work_keys_str_mv AT bushmatthewj hyphalcompartmentalizationandsporulationinstreptomycesrequiretheconservedcelldivisionproteinsepx
AT gallagherkelleya hyphalcompartmentalizationandsporulationinstreptomycesrequiretheconservedcelldivisionproteinsepx
AT chandragovind hyphalcompartmentalizationandsporulationinstreptomycesrequiretheconservedcelldivisionproteinsepx
AT findlaykimc hyphalcompartmentalizationandsporulationinstreptomycesrequiretheconservedcelldivisionproteinsepx
AT schlimpertsusan hyphalcompartmentalizationandsporulationinstreptomycesrequiretheconservedcelldivisionproteinsepx