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Auxin‐induced actin cytoskeleton rearrangements require AUX1

The actin cytoskeleton is required for cell expansion and implicated in cellular responses to the phytohormone auxin. However, the mechanisms that coordinate auxin signaling, cytoskeletal remodeling and cell expansion are poorly understood. Previous studies examined long‐term actin cytoskeleton resp...

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Detalles Bibliográficos
Autores principales: Arieti, Ruthie S., Staiger, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154765/
https://www.ncbi.nlm.nih.gov/pubmed/31859367
http://dx.doi.org/10.1111/nph.16382
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author Arieti, Ruthie S.
Staiger, Christopher J.
author_facet Arieti, Ruthie S.
Staiger, Christopher J.
author_sort Arieti, Ruthie S.
collection PubMed
description The actin cytoskeleton is required for cell expansion and implicated in cellular responses to the phytohormone auxin. However, the mechanisms that coordinate auxin signaling, cytoskeletal remodeling and cell expansion are poorly understood. Previous studies examined long‐term actin cytoskeleton responses to auxin, but plants respond to auxin within minutes. Before this work, an extracellular auxin receptor – rather than the auxin transporter AUXIN RESISTANT 1 (AUX1) – was considered to precede auxin‐induced cytoskeleton reorganization. In order to correlate actin array organization and dynamics with degree of cell expansion, quantitative imaging tools established baseline actin organization and illuminated individual filament behaviors in root epidermal cells under control conditions and after indole‐3‐acetic acid (IAA) application. We evaluated aux1 mutant actin organization responses to IAA and the membrane‐permeable auxin 1‐naphthylacetic acid (NAA). Cell length predicted actin organization and dynamics in control roots; short‐term IAA treatments stimulated denser and more parallel, longitudinal arrays by inducing filament unbundling within minutes. Although AUX1 is necessary for full actin rearrangements in response to auxin, cytoplasmic auxin (i.e. NAA) stimulated a lesser response. Actin filaments became more ‘organized’ after IAA stopped elongation, refuting the hypothesis that ‘more organized’ actin arrays universally correlate with rapid growth. Short‐term actin cytoskeleton response to auxin requires AUX1 and/or cytoplasmic auxin.
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spelling pubmed-71547652020-04-15 Auxin‐induced actin cytoskeleton rearrangements require AUX1 Arieti, Ruthie S. Staiger, Christopher J. New Phytol Research The actin cytoskeleton is required for cell expansion and implicated in cellular responses to the phytohormone auxin. However, the mechanisms that coordinate auxin signaling, cytoskeletal remodeling and cell expansion are poorly understood. Previous studies examined long‐term actin cytoskeleton responses to auxin, but plants respond to auxin within minutes. Before this work, an extracellular auxin receptor – rather than the auxin transporter AUXIN RESISTANT 1 (AUX1) – was considered to precede auxin‐induced cytoskeleton reorganization. In order to correlate actin array organization and dynamics with degree of cell expansion, quantitative imaging tools established baseline actin organization and illuminated individual filament behaviors in root epidermal cells under control conditions and after indole‐3‐acetic acid (IAA) application. We evaluated aux1 mutant actin organization responses to IAA and the membrane‐permeable auxin 1‐naphthylacetic acid (NAA). Cell length predicted actin organization and dynamics in control roots; short‐term IAA treatments stimulated denser and more parallel, longitudinal arrays by inducing filament unbundling within minutes. Although AUX1 is necessary for full actin rearrangements in response to auxin, cytoplasmic auxin (i.e. NAA) stimulated a lesser response. Actin filaments became more ‘organized’ after IAA stopped elongation, refuting the hypothesis that ‘more organized’ actin arrays universally correlate with rapid growth. Short‐term actin cytoskeleton response to auxin requires AUX1 and/or cytoplasmic auxin. John Wiley and Sons Inc. 2020-02-11 2020-04 /pmc/articles/PMC7154765/ /pubmed/31859367 http://dx.doi.org/10.1111/nph.16382 Text en © 2019 The Authors. New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Arieti, Ruthie S.
Staiger, Christopher J.
Auxin‐induced actin cytoskeleton rearrangements require AUX1
title Auxin‐induced actin cytoskeleton rearrangements require AUX1
title_full Auxin‐induced actin cytoskeleton rearrangements require AUX1
title_fullStr Auxin‐induced actin cytoskeleton rearrangements require AUX1
title_full_unstemmed Auxin‐induced actin cytoskeleton rearrangements require AUX1
title_short Auxin‐induced actin cytoskeleton rearrangements require AUX1
title_sort auxin‐induced actin cytoskeleton rearrangements require aux1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154765/
https://www.ncbi.nlm.nih.gov/pubmed/31859367
http://dx.doi.org/10.1111/nph.16382
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