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Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria

Many filamentous organisms, such as fungi, grow by tip-extension and by forming new branches behind the tips. A similar growth mode occurs in filamentous bacteria, including the genus Streptomyces, although here our mechanistic understanding has been very limited. The Streptomyces protein DivIVA is...

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Autores principales: Richards, David M., Hempel, Antje M., Flärdh, Klas, Buttner, Mark J., Howard, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297577/
https://www.ncbi.nlm.nih.gov/pubmed/22423220
http://dx.doi.org/10.1371/journal.pcbi.1002423
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author Richards, David M.
Hempel, Antje M.
Flärdh, Klas
Buttner, Mark J.
Howard, Martin
author_facet Richards, David M.
Hempel, Antje M.
Flärdh, Klas
Buttner, Mark J.
Howard, Martin
author_sort Richards, David M.
collection PubMed
description Many filamentous organisms, such as fungi, grow by tip-extension and by forming new branches behind the tips. A similar growth mode occurs in filamentous bacteria, including the genus Streptomyces, although here our mechanistic understanding has been very limited. The Streptomyces protein DivIVA is a critical determinant of hyphal growth and localizes in foci at hyphal tips and sites of future branch development. However, how such foci form was previously unknown. Here, we show experimentally that DivIVA focus-formation involves a novel mechanism in which new DivIVA foci break off from existing tip-foci, bypassing the need for initial nucleation or de novo branch-site selection. We develop a mathematical model for DivIVA-dependent growth and branching, involving DivIVA focus-formation by tip-focus splitting, focus growth, and the initiation of new branches at a critical focus size. We quantitatively fit our model to the experimentally-measured tip-to-branch and branch-to-branch length distributions. The model predicts a particular bimodal tip-to-branch distribution results from tip-focus splitting, a prediction we confirm experimentally. Our work provides mechanistic understanding of a novel mode of hyphal growth regulation that may be widely employed.
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spelling pubmed-32975772012-03-15 Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria Richards, David M. Hempel, Antje M. Flärdh, Klas Buttner, Mark J. Howard, Martin PLoS Comput Biol Research Article Many filamentous organisms, such as fungi, grow by tip-extension and by forming new branches behind the tips. A similar growth mode occurs in filamentous bacteria, including the genus Streptomyces, although here our mechanistic understanding has been very limited. The Streptomyces protein DivIVA is a critical determinant of hyphal growth and localizes in foci at hyphal tips and sites of future branch development. However, how such foci form was previously unknown. Here, we show experimentally that DivIVA focus-formation involves a novel mechanism in which new DivIVA foci break off from existing tip-foci, bypassing the need for initial nucleation or de novo branch-site selection. We develop a mathematical model for DivIVA-dependent growth and branching, involving DivIVA focus-formation by tip-focus splitting, focus growth, and the initiation of new branches at a critical focus size. We quantitatively fit our model to the experimentally-measured tip-to-branch and branch-to-branch length distributions. The model predicts a particular bimodal tip-to-branch distribution results from tip-focus splitting, a prediction we confirm experimentally. Our work provides mechanistic understanding of a novel mode of hyphal growth regulation that may be widely employed. Public Library of Science 2012-03-08 /pmc/articles/PMC3297577/ /pubmed/22423220 http://dx.doi.org/10.1371/journal.pcbi.1002423 Text en Richards et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Richards, David M.
Hempel, Antje M.
Flärdh, Klas
Buttner, Mark J.
Howard, Martin
Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title_full Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title_fullStr Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title_full_unstemmed Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title_short Mechanistic Basis of Branch-Site Selection in Filamentous Bacteria
title_sort mechanistic basis of branch-site selection in filamentous bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297577/
https://www.ncbi.nlm.nih.gov/pubmed/22423220
http://dx.doi.org/10.1371/journal.pcbi.1002423
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