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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2007
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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 |
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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 |
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