Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1782225892006690816 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3297577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT richardsdavidm mechanisticbasisofbranchsiteselectioninfilamentousbacteria AT hempelantjem mechanisticbasisofbranchsiteselectioninfilamentousbacteria AT flardhklas mechanisticbasisofbranchsiteselectioninfilamentousbacteria AT buttnermarkj mechanisticbasisofbranchsiteselectioninfilamentousbacteria AT howardmartin mechanisticbasisofbranchsiteselectioninfilamentousbacteria |