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Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array
Metazoan cells harness the power of actin dynamics to create cytoskeletal arrays that stimulate protrusions and drive intracellular organelle movements. In plant cells, the actin cytoskeleton is understood to participate in cell elongation; however, a detailed description and molecular mechanism(s)...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654301/ https://www.ncbi.nlm.nih.gov/pubmed/19171759 http://dx.doi.org/10.1083/jcb.200806185 |
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author | Staiger, Christopher J. Sheahan, Michael B. Khurana, Parul Wang, Xia McCurdy, David W. Blanchoin, Laurent |
author_facet | Staiger, Christopher J. Sheahan, Michael B. Khurana, Parul Wang, Xia McCurdy, David W. Blanchoin, Laurent |
author_sort | Staiger, Christopher J. |
collection | PubMed |
description | Metazoan cells harness the power of actin dynamics to create cytoskeletal arrays that stimulate protrusions and drive intracellular organelle movements. In plant cells, the actin cytoskeleton is understood to participate in cell elongation; however, a detailed description and molecular mechanism(s) underpinning filament nucleation, growth, and turnover are lacking. Here, we use variable-angle epifluorescence microscopy (VAEM) to examine the organization and dynamics of the cortical cytoskeleton in growing and nongrowing epidermal cells. One population of filaments in the cortical array, which most likely represent single actin filaments, is randomly oriented and highly dynamic. These filaments grow at rates of 1.7 µm/s, but are generally short-lived. Instead of depolymerization at their ends, actin filaments are disassembled by severing activity. Remodeling of the cortical actin array also features filament buckling and straightening events. These observations indicate a mechanism inconsistent with treadmilling. Instead, cortical actin filament dynamics resemble the stochastic dynamics of an in vitro biomimetic system for actin assembly. |
format | Text |
id | pubmed-2654301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26543012009-07-26 Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array Staiger, Christopher J. Sheahan, Michael B. Khurana, Parul Wang, Xia McCurdy, David W. Blanchoin, Laurent J Cell Biol Research Articles Metazoan cells harness the power of actin dynamics to create cytoskeletal arrays that stimulate protrusions and drive intracellular organelle movements. In plant cells, the actin cytoskeleton is understood to participate in cell elongation; however, a detailed description and molecular mechanism(s) underpinning filament nucleation, growth, and turnover are lacking. Here, we use variable-angle epifluorescence microscopy (VAEM) to examine the organization and dynamics of the cortical cytoskeleton in growing and nongrowing epidermal cells. One population of filaments in the cortical array, which most likely represent single actin filaments, is randomly oriented and highly dynamic. These filaments grow at rates of 1.7 µm/s, but are generally short-lived. Instead of depolymerization at their ends, actin filaments are disassembled by severing activity. Remodeling of the cortical actin array also features filament buckling and straightening events. These observations indicate a mechanism inconsistent with treadmilling. Instead, cortical actin filament dynamics resemble the stochastic dynamics of an in vitro biomimetic system for actin assembly. The Rockefeller University Press 2009-01-26 /pmc/articles/PMC2654301/ /pubmed/19171759 http://dx.doi.org/10.1083/jcb.200806185 Text en © 2009 Staiger et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Staiger, Christopher J. Sheahan, Michael B. Khurana, Parul Wang, Xia McCurdy, David W. Blanchoin, Laurent Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title | Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title_full | Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title_fullStr | Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title_full_unstemmed | Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title_short | Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array |
title_sort | actin filament dynamics are dominated by rapid growth and severing activity in the arabidopsis cortical array |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654301/ https://www.ncbi.nlm.nih.gov/pubmed/19171759 http://dx.doi.org/10.1083/jcb.200806185 |
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