Cargando…

Function of the anion transporter AtCLC-d in the trans-Golgi network

Anion transporting proteins of the CLC type are involved in anion homeostasis in a variety of organisms. CLCs from Arabidopsis have been shown to participate in nitrate accumulation and storage. In this study, the physiological role of the functional chloride transporter AtCLC-d from Arabidopsis was...

Descripción completa

Detalles Bibliográficos
Autores principales: von der Fecht-Bartenbach, Jennifer, Bogner, Martin, Krebs, Melanie, Stierhof, York-Dieter, Schumacher, Karin, Ludewig, Uwe
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891005/
https://www.ncbi.nlm.nih.gov/pubmed/17376158
http://dx.doi.org/10.1111/j.1365-313X.2007.03061.x
_version_ 1782133726644273152
author von der Fecht-Bartenbach, Jennifer
Bogner, Martin
Krebs, Melanie
Stierhof, York-Dieter
Schumacher, Karin
Ludewig, Uwe
author_facet von der Fecht-Bartenbach, Jennifer
Bogner, Martin
Krebs, Melanie
Stierhof, York-Dieter
Schumacher, Karin
Ludewig, Uwe
author_sort von der Fecht-Bartenbach, Jennifer
collection PubMed
description Anion transporting proteins of the CLC type are involved in anion homeostasis in a variety of organisms. CLCs from Arabidopsis have been shown to participate in nitrate accumulation and storage. In this study, the physiological role of the functional chloride transporter AtCLC-d from Arabidopsis was investigated. AtCLC-d is weakly expressed in various tissues, including the root. When transiently expressed as a GFP fusion in protoplasts, it co-localized with the VHA-a1 subunit of the proton-transporting V-type ATPase in the trans-Golgi network (TGN). Stable expression in plants showed that it co-localized with the endocytic tracer dye FM4-64 in a brefeldin A-sensitive compartment. Immunogold electron microscopy confirmed the localization of AtCLC-d to the TGN. Disruption of the AtCLC-d gene by a T-DNA insertion did not affect the nitrate and chloride contents. The overall morphology of these clcd-1 plants was similar to that of the wild-type, but root growth on synthetic medium was impaired. Moreover, the sensitivity of hypocotyl elongation to treatment with concanamycin A, a blocker of the V-ATPase, was stronger in the clcd-1 mutant. These phenotypes could be complemented by overexpression of AtCLC-d in the mutant background. The results suggest that the luminal pH in the trans-Golgi network is adjusted by AtCLC-d-mediated transport of a counter anion such as Cl(−) or NO(3)(−).
format Text
id pubmed-1891005
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-18910052007-06-18 Function of the anion transporter AtCLC-d in the trans-Golgi network von der Fecht-Bartenbach, Jennifer Bogner, Martin Krebs, Melanie Stierhof, York-Dieter Schumacher, Karin Ludewig, Uwe Plant J Original Articles Anion transporting proteins of the CLC type are involved in anion homeostasis in a variety of organisms. CLCs from Arabidopsis have been shown to participate in nitrate accumulation and storage. In this study, the physiological role of the functional chloride transporter AtCLC-d from Arabidopsis was investigated. AtCLC-d is weakly expressed in various tissues, including the root. When transiently expressed as a GFP fusion in protoplasts, it co-localized with the VHA-a1 subunit of the proton-transporting V-type ATPase in the trans-Golgi network (TGN). Stable expression in plants showed that it co-localized with the endocytic tracer dye FM4-64 in a brefeldin A-sensitive compartment. Immunogold electron microscopy confirmed the localization of AtCLC-d to the TGN. Disruption of the AtCLC-d gene by a T-DNA insertion did not affect the nitrate and chloride contents. The overall morphology of these clcd-1 plants was similar to that of the wild-type, but root growth on synthetic medium was impaired. Moreover, the sensitivity of hypocotyl elongation to treatment with concanamycin A, a blocker of the V-ATPase, was stronger in the clcd-1 mutant. These phenotypes could be complemented by overexpression of AtCLC-d in the mutant background. The results suggest that the luminal pH in the trans-Golgi network is adjusted by AtCLC-d-mediated transport of a counter anion such as Cl(−) or NO(3)(−). Blackwell Publishing Ltd 2007-05-01 /pmc/articles/PMC1891005/ /pubmed/17376158 http://dx.doi.org/10.1111/j.1365-313X.2007.03061.x Text en © 2007 The Authors Journal compilation © 2007 Blackwell Publishing Ltd
spellingShingle Original Articles
von der Fecht-Bartenbach, Jennifer
Bogner, Martin
Krebs, Melanie
Stierhof, York-Dieter
Schumacher, Karin
Ludewig, Uwe
Function of the anion transporter AtCLC-d in the trans-Golgi network
title Function of the anion transporter AtCLC-d in the trans-Golgi network
title_full Function of the anion transporter AtCLC-d in the trans-Golgi network
title_fullStr Function of the anion transporter AtCLC-d in the trans-Golgi network
title_full_unstemmed Function of the anion transporter AtCLC-d in the trans-Golgi network
title_short Function of the anion transporter AtCLC-d in the trans-Golgi network
title_sort function of the anion transporter atclc-d in the trans-golgi network
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891005/
https://www.ncbi.nlm.nih.gov/pubmed/17376158
http://dx.doi.org/10.1111/j.1365-313X.2007.03061.x
work_keys_str_mv AT vonderfechtbartenbachjennifer functionoftheaniontransporteratclcdinthetransgolginetwork
AT bognermartin functionoftheaniontransporteratclcdinthetransgolginetwork
AT krebsmelanie functionoftheaniontransporteratclcdinthetransgolginetwork
AT stierhofyorkdieter functionoftheaniontransporteratclcdinthetransgolginetwork
AT schumacherkarin functionoftheaniontransporteratclcdinthetransgolginetwork
AT ludewiguwe functionoftheaniontransporteratclcdinthetransgolginetwork