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A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs

Phosphatidylinositol (PtdIns) transfer proteins (PITPs) regulate signaling interfaces between lipid metabolism and membrane trafficking. Herein, we demonstrate that AtSfh1p, a member of a large and uncharacterized Arabidopsis thaliana Sec14p-nodulin domain family, is a PITP that regulates a specific...

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Autores principales: Vincent, Patrick, Chua, Michael, Nogue, Fabien, Fairbrother, Ashley, Mekeel, Hal, Xu, Yue, Allen, Nina, Bibikova, Tatiana N., Gilroy, Simon, Bankaitis, Vytas A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171805/
https://www.ncbi.nlm.nih.gov/pubmed/15728190
http://dx.doi.org/10.1083/jcb.200412074
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author Vincent, Patrick
Chua, Michael
Nogue, Fabien
Fairbrother, Ashley
Mekeel, Hal
Xu, Yue
Allen, Nina
Bibikova, Tatiana N.
Gilroy, Simon
Bankaitis, Vytas A.
author_facet Vincent, Patrick
Chua, Michael
Nogue, Fabien
Fairbrother, Ashley
Mekeel, Hal
Xu, Yue
Allen, Nina
Bibikova, Tatiana N.
Gilroy, Simon
Bankaitis, Vytas A.
author_sort Vincent, Patrick
collection PubMed
description Phosphatidylinositol (PtdIns) transfer proteins (PITPs) regulate signaling interfaces between lipid metabolism and membrane trafficking. Herein, we demonstrate that AtSfh1p, a member of a large and uncharacterized Arabidopsis thaliana Sec14p-nodulin domain family, is a PITP that regulates a specific stage in root hair development. AtSfh1p localizes along the root hair plasma membrane and is enriched in discrete plasma membrane domains and in the root hair tip cytoplasm. This localization pattern recapitulates that visualized for PtdIns(4,5)P(2) in developing root hairs. Gene ablation experiments show AtSfh1p nullizygosity compromises polarized root hair expansion in a manner that coincides with loss of tip-directed PtdIns(4,5)P(2), dispersal of secretory vesicles from the tip cytoplasm, loss of the tip f-actin network, and manifest disorganization of the root hair microtubule cytoskeleton. Derangement of tip-directed Ca(2+) gradients is also apparent and results from isotropic influx of Ca(2+) from the extracellular milieu. We propose AtSfh1p regulates intracellular and plasma membrane phosphoinositide polarity landmarks that focus membrane trafficking, Ca(2+) signaling, and cytoskeleton functions to the growing root hair apex. We further suggest that Sec14p-nodulin domain proteins represent a family of regulators of polarized membrane growth in plants.
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spelling pubmed-21718052008-03-05 A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs Vincent, Patrick Chua, Michael Nogue, Fabien Fairbrother, Ashley Mekeel, Hal Xu, Yue Allen, Nina Bibikova, Tatiana N. Gilroy, Simon Bankaitis, Vytas A. J Cell Biol Research Articles Phosphatidylinositol (PtdIns) transfer proteins (PITPs) regulate signaling interfaces between lipid metabolism and membrane trafficking. Herein, we demonstrate that AtSfh1p, a member of a large and uncharacterized Arabidopsis thaliana Sec14p-nodulin domain family, is a PITP that regulates a specific stage in root hair development. AtSfh1p localizes along the root hair plasma membrane and is enriched in discrete plasma membrane domains and in the root hair tip cytoplasm. This localization pattern recapitulates that visualized for PtdIns(4,5)P(2) in developing root hairs. Gene ablation experiments show AtSfh1p nullizygosity compromises polarized root hair expansion in a manner that coincides with loss of tip-directed PtdIns(4,5)P(2), dispersal of secretory vesicles from the tip cytoplasm, loss of the tip f-actin network, and manifest disorganization of the root hair microtubule cytoskeleton. Derangement of tip-directed Ca(2+) gradients is also apparent and results from isotropic influx of Ca(2+) from the extracellular milieu. We propose AtSfh1p regulates intracellular and plasma membrane phosphoinositide polarity landmarks that focus membrane trafficking, Ca(2+) signaling, and cytoskeleton functions to the growing root hair apex. We further suggest that Sec14p-nodulin domain proteins represent a family of regulators of polarized membrane growth in plants. The Rockefeller University Press 2005-02-28 /pmc/articles/PMC2171805/ /pubmed/15728190 http://dx.doi.org/10.1083/jcb.200412074 Text en Copyright © 2005, The Rockefeller University Press 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.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Vincent, Patrick
Chua, Michael
Nogue, Fabien
Fairbrother, Ashley
Mekeel, Hal
Xu, Yue
Allen, Nina
Bibikova, Tatiana N.
Gilroy, Simon
Bankaitis, Vytas A.
A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title_full A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title_fullStr A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title_full_unstemmed A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title_short A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs
title_sort sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of arabidopsis thaliana root hairs
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171805/
https://www.ncbi.nlm.nih.gov/pubmed/15728190
http://dx.doi.org/10.1083/jcb.200412074
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