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A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans
Transient Receptor Potential (TRP) proteins constitute a superfamily that encodes transmembrane ion channels with highly diverse permeation and gating properties. Filamentous fungi possess putative TRP channel-encoded genes, but their functions remain elusive. Here, we report that a putative TRP-lik...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618638/ https://www.ncbi.nlm.nih.gov/pubmed/34829209 http://dx.doi.org/10.3390/jof7110920 |
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author | Wang, Hongchen Chen, Qiuyi Zhang, Shizhu Lu, Ling |
author_facet | Wang, Hongchen Chen, Qiuyi Zhang, Shizhu Lu, Ling |
author_sort | Wang, Hongchen |
collection | PubMed |
description | Transient Receptor Potential (TRP) proteins constitute a superfamily that encodes transmembrane ion channels with highly diverse permeation and gating properties. Filamentous fungi possess putative TRP channel-encoded genes, but their functions remain elusive. Here, we report that a putative TRP-like calcium channel, trpR, in the filamentous fungus Aspergillus nidulans, performs important roles in conidiation and in adapting to cell wall disruption reagents in a high temperature-induced defect-dependent manner, especially under a calcium-limited culture condition. The genetic and functional relationship between TrpR and the previously identified high-affinity calcium channels CchA/MidA indicates that TrpR has an opposite response to CchA/MidA when reacting to cell wall disruption reagents and in regulating calcium transients. However, a considerable addition of calcium can rescue all the defects that occur in TrpR and CchA/MidA, meaning that calcium is able to bypass the necessary requirement. Nevertheless, the colocalization at the membrane of the Golgi for TrpR and the P-type Golgi Ca(2+) ATPase PmrA suggests two channels that may work as ion transporters, transferring Ca(2+) from the cytosol into the Golgi apparatus and maintaining cellular calcium homeostasis. Therefore, combined with data for the trpR deletion mutant revealing abnormal cell wall structures, TrpR works as a Golgi membrane calcium ion channel that involves cell wall integration. |
format | Online Article Text |
id | pubmed-8618638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86186382021-11-27 A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans Wang, Hongchen Chen, Qiuyi Zhang, Shizhu Lu, Ling J Fungi (Basel) Article Transient Receptor Potential (TRP) proteins constitute a superfamily that encodes transmembrane ion channels with highly diverse permeation and gating properties. Filamentous fungi possess putative TRP channel-encoded genes, but their functions remain elusive. Here, we report that a putative TRP-like calcium channel, trpR, in the filamentous fungus Aspergillus nidulans, performs important roles in conidiation and in adapting to cell wall disruption reagents in a high temperature-induced defect-dependent manner, especially under a calcium-limited culture condition. The genetic and functional relationship between TrpR and the previously identified high-affinity calcium channels CchA/MidA indicates that TrpR has an opposite response to CchA/MidA when reacting to cell wall disruption reagents and in regulating calcium transients. However, a considerable addition of calcium can rescue all the defects that occur in TrpR and CchA/MidA, meaning that calcium is able to bypass the necessary requirement. Nevertheless, the colocalization at the membrane of the Golgi for TrpR and the P-type Golgi Ca(2+) ATPase PmrA suggests two channels that may work as ion transporters, transferring Ca(2+) from the cytosol into the Golgi apparatus and maintaining cellular calcium homeostasis. Therefore, combined with data for the trpR deletion mutant revealing abnormal cell wall structures, TrpR works as a Golgi membrane calcium ion channel that involves cell wall integration. MDPI 2021-10-28 /pmc/articles/PMC8618638/ /pubmed/34829209 http://dx.doi.org/10.3390/jof7110920 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Hongchen Chen, Qiuyi Zhang, Shizhu Lu, Ling A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title | A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title_full | A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title_fullStr | A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title_full_unstemmed | A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title_short | A Transient Receptor Potential-like Calcium Ion Channel in the Filamentous Fungus Aspergillus nidulans |
title_sort | transient receptor potential-like calcium ion channel in the filamentous fungus aspergillus nidulans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618638/ https://www.ncbi.nlm.nih.gov/pubmed/34829209 http://dx.doi.org/10.3390/jof7110920 |
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