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Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals
Neuronal resting potential can tune the excitability of neural networks, affecting downstream behavior. Sodium leak channels (NALCN) play a key role in rhythmic behaviors by helping set, or subtly changing neuronal resting potential. The full complexity of these newly described channels is just begi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945613/ https://www.ncbi.nlm.nih.gov/pubmed/24639627 http://dx.doi.org/10.3389/fnmol.2014.00015 |
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author | Ghezzi, Alfredo Liebeskind, Benjamin J. Thompson, Ammon Atkinson, Nigel S. Zakon, Harold H. |
author_facet | Ghezzi, Alfredo Liebeskind, Benjamin J. Thompson, Ammon Atkinson, Nigel S. Zakon, Harold H. |
author_sort | Ghezzi, Alfredo |
collection | PubMed |
description | Neuronal resting potential can tune the excitability of neural networks, affecting downstream behavior. Sodium leak channels (NALCN) play a key role in rhythmic behaviors by helping set, or subtly changing neuronal resting potential. The full complexity of these newly described channels is just beginning to be appreciated, however. NALCN channels can associate with numerous subunits in different tissues and can be activated by several different peptides and second messengers. We recently showed that NALCN channels are closely related to fungal calcium channels, which they functionally resemble. Here, we use this relationship to predict a family of NALCN-associated proteins in animals on the basis of homology with the yeast protein Mid1, the subunit of the yeast calcium channel. These proteins all share a cysteine-rich region that is necessary for Mid1 function in yeast. We validate this predicted association by showing that the Mid1 homolog in Drosophila, encoded by the CG33988 gene, is coordinately expressed with NALCN, and that knockdown of either protein creates identical phenotypes in several behaviors associated with NALCN function. The relationship between Mid1 and leak channels has therefore persisted over a billion years of evolution, despite drastic changes to both proteins and the organisms in which they exist. |
format | Online Article Text |
id | pubmed-3945613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39456132014-03-17 Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals Ghezzi, Alfredo Liebeskind, Benjamin J. Thompson, Ammon Atkinson, Nigel S. Zakon, Harold H. Front Mol Neurosci Neuroscience Neuronal resting potential can tune the excitability of neural networks, affecting downstream behavior. Sodium leak channels (NALCN) play a key role in rhythmic behaviors by helping set, or subtly changing neuronal resting potential. The full complexity of these newly described channels is just beginning to be appreciated, however. NALCN channels can associate with numerous subunits in different tissues and can be activated by several different peptides and second messengers. We recently showed that NALCN channels are closely related to fungal calcium channels, which they functionally resemble. Here, we use this relationship to predict a family of NALCN-associated proteins in animals on the basis of homology with the yeast protein Mid1, the subunit of the yeast calcium channel. These proteins all share a cysteine-rich region that is necessary for Mid1 function in yeast. We validate this predicted association by showing that the Mid1 homolog in Drosophila, encoded by the CG33988 gene, is coordinately expressed with NALCN, and that knockdown of either protein creates identical phenotypes in several behaviors associated with NALCN function. The relationship between Mid1 and leak channels has therefore persisted over a billion years of evolution, despite drastic changes to both proteins and the organisms in which they exist. Frontiers Media S.A. 2014-03-07 /pmc/articles/PMC3945613/ /pubmed/24639627 http://dx.doi.org/10.3389/fnmol.2014.00015 Text en Copyright © 2014 Ghezzi, Liebeskind, Thompson, Atkinson and Zakon. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Ghezzi, Alfredo Liebeskind, Benjamin J. Thompson, Ammon Atkinson, Nigel S. Zakon, Harold H. Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title | Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title_full | Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title_fullStr | Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title_full_unstemmed | Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title_short | Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals |
title_sort | ancient association between cation leak channels and mid1 proteins is conserved in fungi and animals |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945613/ https://www.ncbi.nlm.nih.gov/pubmed/24639627 http://dx.doi.org/10.3389/fnmol.2014.00015 |
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