Cargando…

EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance

Endocytosis is a crucial process in all eukaryotic organisms including plants. We have previously shown that two Arabidopsis proteins, AtEHD1 and AtEHD2, are involved in endocytosis in plant systems. Knock-down of EHD1 was shown to have a delayed recycling phenotype in mammalians. There are many wor...

Descripción completa

Detalles Bibliográficos
Autores principales: Bar, Maya, Leibman, Meirav, Schuster, Silvia, Pitzhadza, Hilla, Avni, Adi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544766/
https://www.ncbi.nlm.nih.gov/pubmed/23342166
http://dx.doi.org/10.1371/journal.pone.0054533
_version_ 1782255846691962880
author Bar, Maya
Leibman, Meirav
Schuster, Silvia
Pitzhadza, Hilla
Avni, Adi
author_facet Bar, Maya
Leibman, Meirav
Schuster, Silvia
Pitzhadza, Hilla
Avni, Adi
author_sort Bar, Maya
collection PubMed
description Endocytosis is a crucial process in all eukaryotic organisms including plants. We have previously shown that two Arabidopsis proteins, AtEHD1 and AtEHD2, are involved in endocytosis in plant systems. Knock-down of EHD1 was shown to have a delayed recycling phenotype in mammalians. There are many works in mammalian systems detailing the importance of the various domains in EHDs but, to date, the domains of plant EHD1 that are required for its activity have not been characterized. In this work we demonstrate that knock-down of EHD1 causes a delayed recycling phenotype and reduces Brefeldin A sensitivity in Arabidopsis seedlings. The EH domain of EHD1 was found to be crucial for the localization of EHD1 to endosomal structures. Mutant EHD1 lacking the EH domain did not localize to endosomal structures and showed a phenotype similar to that of EHD1 knock-down seedlings. Mutants lacking the coiled-coil domain, however, showed a phenotype similar to wild-type or EHD1 overexpression seedlings. Salinity stress is a major problem in current agriculture. Microarray data demonstrated that salinity stress enhances the expression of EHD1, and this was confirmed by semi quantitative RT-PCR. We demonstrate herein that transgenic plants over expressing EHD1 possess enhanced tolerance to salt stress, a property which also requires an intact EH domain.
format Online
Article
Text
id pubmed-3544766
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35447662013-01-22 EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance Bar, Maya Leibman, Meirav Schuster, Silvia Pitzhadza, Hilla Avni, Adi PLoS One Research Article Endocytosis is a crucial process in all eukaryotic organisms including plants. We have previously shown that two Arabidopsis proteins, AtEHD1 and AtEHD2, are involved in endocytosis in plant systems. Knock-down of EHD1 was shown to have a delayed recycling phenotype in mammalians. There are many works in mammalian systems detailing the importance of the various domains in EHDs but, to date, the domains of plant EHD1 that are required for its activity have not been characterized. In this work we demonstrate that knock-down of EHD1 causes a delayed recycling phenotype and reduces Brefeldin A sensitivity in Arabidopsis seedlings. The EH domain of EHD1 was found to be crucial for the localization of EHD1 to endosomal structures. Mutant EHD1 lacking the EH domain did not localize to endosomal structures and showed a phenotype similar to that of EHD1 knock-down seedlings. Mutants lacking the coiled-coil domain, however, showed a phenotype similar to wild-type or EHD1 overexpression seedlings. Salinity stress is a major problem in current agriculture. Microarray data demonstrated that salinity stress enhances the expression of EHD1, and this was confirmed by semi quantitative RT-PCR. We demonstrate herein that transgenic plants over expressing EHD1 possess enhanced tolerance to salt stress, a property which also requires an intact EH domain. Public Library of Science 2013-01-14 /pmc/articles/PMC3544766/ /pubmed/23342166 http://dx.doi.org/10.1371/journal.pone.0054533 Text en © 2013 Bar 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
Bar, Maya
Leibman, Meirav
Schuster, Silvia
Pitzhadza, Hilla
Avni, Adi
EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title_full EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title_fullStr EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title_full_unstemmed EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title_short EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance
title_sort ehd1 functions in endosomal recycling and confers salt tolerance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544766/
https://www.ncbi.nlm.nih.gov/pubmed/23342166
http://dx.doi.org/10.1371/journal.pone.0054533
work_keys_str_mv AT barmaya ehd1functionsinendosomalrecyclingandconferssalttolerance
AT leibmanmeirav ehd1functionsinendosomalrecyclingandconferssalttolerance
AT schustersilvia ehd1functionsinendosomalrecyclingandconferssalttolerance
AT pitzhadzahilla ehd1functionsinendosomalrecyclingandconferssalttolerance
AT avniadi ehd1functionsinendosomalrecyclingandconferssalttolerance