Cargando…
The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth
Fungal hyphae are among the most highly polarized cells. Hyphal polarized growth is supported by tip-directed transport of secretory vesicles, which accumulate temporarily in a stratified manner in an apical vesicle cluster, the Spitzenkörper. The exocyst complex is required for tethering of secreto...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982996/ https://www.ncbi.nlm.nih.gov/pubmed/24523289 http://dx.doi.org/10.1091/mbc.E13-06-0299 |
_version_ | 1782311238545440768 |
---|---|
author | Riquelme, Meritxell Bredeweg, Erin L. Callejas-Negrete, Olga Roberson, Robert W. Ludwig, Sarah Beltrán-Aguilar, Alejandro Seiler, Stephan Novick, Peter Freitag, Michael |
author_facet | Riquelme, Meritxell Bredeweg, Erin L. Callejas-Negrete, Olga Roberson, Robert W. Ludwig, Sarah Beltrán-Aguilar, Alejandro Seiler, Stephan Novick, Peter Freitag, Michael |
author_sort | Riquelme, Meritxell |
collection | PubMed |
description | Fungal hyphae are among the most highly polarized cells. Hyphal polarized growth is supported by tip-directed transport of secretory vesicles, which accumulate temporarily in a stratified manner in an apical vesicle cluster, the Spitzenkörper. The exocyst complex is required for tethering of secretory vesicles to the apical plasma membrane. We determined that the presence of an octameric exocyst complex is required for the formation of a functional Spitzenkörper and maintenance of regular hyphal growth in Neurospora crassa. Two distinct localization patterns of exocyst subunits at the hyphal tip suggest the dynamic formation of two assemblies. The EXO-70/EXO-84 subunits are found at the peripheral part of the Spitzenkörper, which partially coincides with the outer macrovesicular layer, whereas exocyst components SEC-5, -6, -8, and -15 form a delimited crescent at the apical plasma membrane. Localization of SEC-6 and EXO-70 to the plasma membrane and the Spitzenkörper, respectively, depends on actin and microtubule cytoskeletons. The apical region of exocyst-mediated vesicle fusion, elucidated by the plasma membrane–associated exocyst subunits, indicates the presence of an exocytotic gradient with a tip-high maximum that dissipates gradually toward the subapex, confirming the earlier predictions of the vesicle supply center model for hyphal morphogenesis. |
format | Online Article Text |
id | pubmed-3982996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39829962014-06-30 The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth Riquelme, Meritxell Bredeweg, Erin L. Callejas-Negrete, Olga Roberson, Robert W. Ludwig, Sarah Beltrán-Aguilar, Alejandro Seiler, Stephan Novick, Peter Freitag, Michael Mol Biol Cell Articles Fungal hyphae are among the most highly polarized cells. Hyphal polarized growth is supported by tip-directed transport of secretory vesicles, which accumulate temporarily in a stratified manner in an apical vesicle cluster, the Spitzenkörper. The exocyst complex is required for tethering of secretory vesicles to the apical plasma membrane. We determined that the presence of an octameric exocyst complex is required for the formation of a functional Spitzenkörper and maintenance of regular hyphal growth in Neurospora crassa. Two distinct localization patterns of exocyst subunits at the hyphal tip suggest the dynamic formation of two assemblies. The EXO-70/EXO-84 subunits are found at the peripheral part of the Spitzenkörper, which partially coincides with the outer macrovesicular layer, whereas exocyst components SEC-5, -6, -8, and -15 form a delimited crescent at the apical plasma membrane. Localization of SEC-6 and EXO-70 to the plasma membrane and the Spitzenkörper, respectively, depends on actin and microtubule cytoskeletons. The apical region of exocyst-mediated vesicle fusion, elucidated by the plasma membrane–associated exocyst subunits, indicates the presence of an exocytotic gradient with a tip-high maximum that dissipates gradually toward the subapex, confirming the earlier predictions of the vesicle supply center model for hyphal morphogenesis. The American Society for Cell Biology 2014-04-15 /pmc/articles/PMC3982996/ /pubmed/24523289 http://dx.doi.org/10.1091/mbc.E13-06-0299 Text en © 2014 Riquelme et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Riquelme, Meritxell Bredeweg, Erin L. Callejas-Negrete, Olga Roberson, Robert W. Ludwig, Sarah Beltrán-Aguilar, Alejandro Seiler, Stephan Novick, Peter Freitag, Michael The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title_full | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title_fullStr | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title_full_unstemmed | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title_short | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth |
title_sort | neurospora crassa exocyst complex tethers spitzenkörper vesicles to the apical plasma membrane during polarized growth |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982996/ https://www.ncbi.nlm.nih.gov/pubmed/24523289 http://dx.doi.org/10.1091/mbc.E13-06-0299 |
work_keys_str_mv | AT riquelmemeritxell theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT bredewegerinl theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT callejasnegreteolga theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT robersonrobertw theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT ludwigsarah theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT beltranaguilaralejandro theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT seilerstephan theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT novickpeter theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT freitagmichael theneurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT riquelmemeritxell neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT bredewegerinl neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT callejasnegreteolga neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT robersonrobertw neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT ludwigsarah neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT beltranaguilaralejandro neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT seilerstephan neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT novickpeter neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth AT freitagmichael neurosporacrassaexocystcomplextethersspitzenkorpervesiclestotheapicalplasmamembraneduringpolarizedgrowth |