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Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels
To fire action-potential-like electrical signals, the vacuole membrane requires the two-pore channel TPC1, formerly called SV channel. The TPC1/SV channel functions as a depolarization-stimulated, non-selective cation channel that is inhibited by luminal Ca(2+). In our search for species-dependent f...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665017/ https://www.ncbi.nlm.nih.gov/pubmed/37991833 http://dx.doi.org/10.7554/eLife.86384 |
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author | Lu, Jinping Dreyer, Ingo Dickinson, Miles Sasha Panzer, Sabine Jaślan, Dawid Navarro-Retamal, Carlos Geiger, Dietmar Terpitz, Ulrich Becker, Dirk Stroud, Robert M Marten, Irene Hedrich, Rainer |
author_facet | Lu, Jinping Dreyer, Ingo Dickinson, Miles Sasha Panzer, Sabine Jaślan, Dawid Navarro-Retamal, Carlos Geiger, Dietmar Terpitz, Ulrich Becker, Dirk Stroud, Robert M Marten, Irene Hedrich, Rainer |
author_sort | Lu, Jinping |
collection | PubMed |
description | To fire action-potential-like electrical signals, the vacuole membrane requires the two-pore channel TPC1, formerly called SV channel. The TPC1/SV channel functions as a depolarization-stimulated, non-selective cation channel that is inhibited by luminal Ca(2+). In our search for species-dependent functional TPC1 channel variants with different luminal Ca(2+) sensitivity, we found in total three acidic residues present in Ca(2+) sensor sites 2 and 3 of the Ca(2+)-sensitive AtTPC1 channel from Arabidopsis thaliana that were neutral in its Vicia faba ortholog and also in those of many other Fabaceae. When expressed in the Arabidopsis AtTPC1-loss-of-function background, wild-type VfTPC1 was hypersensitive to vacuole depolarization and only weakly sensitive to blocking luminal Ca(2+). When AtTPC1 was mutated for these VfTPC1-homologous polymorphic residues, two neutral substitutions in Ca(2+) sensor site 3 alone were already sufficient for the Arabidopsis At-VfTPC1 channel mutant to gain VfTPC1-like voltage and luminal Ca(2+) sensitivity that together rendered vacuoles hyperexcitable. Thus, natural TPC1 channel variants exist in plant families which may fine-tune vacuole excitability and adapt it to environmental settings of the particular ecological niche. |
format | Online Article Text |
id | pubmed-10665017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-106650172023-11-22 Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels Lu, Jinping Dreyer, Ingo Dickinson, Miles Sasha Panzer, Sabine Jaślan, Dawid Navarro-Retamal, Carlos Geiger, Dietmar Terpitz, Ulrich Becker, Dirk Stroud, Robert M Marten, Irene Hedrich, Rainer eLife Plant Biology To fire action-potential-like electrical signals, the vacuole membrane requires the two-pore channel TPC1, formerly called SV channel. The TPC1/SV channel functions as a depolarization-stimulated, non-selective cation channel that is inhibited by luminal Ca(2+). In our search for species-dependent functional TPC1 channel variants with different luminal Ca(2+) sensitivity, we found in total three acidic residues present in Ca(2+) sensor sites 2 and 3 of the Ca(2+)-sensitive AtTPC1 channel from Arabidopsis thaliana that were neutral in its Vicia faba ortholog and also in those of many other Fabaceae. When expressed in the Arabidopsis AtTPC1-loss-of-function background, wild-type VfTPC1 was hypersensitive to vacuole depolarization and only weakly sensitive to blocking luminal Ca(2+). When AtTPC1 was mutated for these VfTPC1-homologous polymorphic residues, two neutral substitutions in Ca(2+) sensor site 3 alone were already sufficient for the Arabidopsis At-VfTPC1 channel mutant to gain VfTPC1-like voltage and luminal Ca(2+) sensitivity that together rendered vacuoles hyperexcitable. Thus, natural TPC1 channel variants exist in plant families which may fine-tune vacuole excitability and adapt it to environmental settings of the particular ecological niche. eLife Sciences Publications, Ltd 2023-11-22 /pmc/articles/PMC10665017/ /pubmed/37991833 http://dx.doi.org/10.7554/eLife.86384 Text en © 2023, Lu et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Plant Biology Lu, Jinping Dreyer, Ingo Dickinson, Miles Sasha Panzer, Sabine Jaślan, Dawid Navarro-Retamal, Carlos Geiger, Dietmar Terpitz, Ulrich Becker, Dirk Stroud, Robert M Marten, Irene Hedrich, Rainer Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title | Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title_full | Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title_fullStr | Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title_full_unstemmed | Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title_short | Vicia faba SV channel VfTPC1 is a hyperexcitable variant of plant vacuole Two Pore Channels |
title_sort | vicia faba sv channel vftpc1 is a hyperexcitable variant of plant vacuole two pore channels |
topic | Plant Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665017/ https://www.ncbi.nlm.nih.gov/pubmed/37991833 http://dx.doi.org/10.7554/eLife.86384 |
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