NALCN/Cch1 channelosome subunits originated in early eukaryotes
NALCN/Cch1 channelosome subunits originated in early eukaryotes
The sodium leak channel NALCN, a key regulator of neuronal excitability, associates with three ancillary subunits that are critical for its function: a subunit called FAM155, which interacts with the extracellular regions of the channel, and two cytoplasmic subunits called UNC79 and UNC80. Interestingly, NALCN and FAM155 have orthologous phylogenetic relationships with the fungal calcium channel Cch1 and its subunit Mid1; however, UNC79 and UNC80 have not been reported outside of animals. In this study, we leveraged expanded gene sequence data available for eukaryotes to reexamine the evolutionary origins of NALCN and Cch1 channel subunits. Our analysis corroborates the direct phylogenetic relationship between NALCN and Cch1 and identifies a larger clade of related channels in additional eukaryotic taxa. We also identify homologues of FAM155/Mid1 in Cryptista algae and UNC79 and UNC80 homologues in numerous non-metazoan eukaryotes, including basidiomycete and mucoromycete fungi and the microbial eukaryotic taxa Apusomonadida, Malawimonadida, and Discoba. Furthermore, we find that most major animal lineages, except ctenophores, possess a full complement of NALCN subunits. Comparing structural predictions with the solved structure of the human NALCN complex supports orthologous relationships between metazoan and non-metazoan FAM155/Mid1, UNC79, and UNC80 homologues. Together, our analyses reveal unexpected diversity and ancient eukaryotic origins of NALCN/Cch1 channelosome subunits and raise interesting questions about the functional nature of this channel complex within a broad, eukaryotic context.
Senatore, Adriano
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Mayorova, Tatiana D.
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Yañez-Guerra, Luis A.
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Elkhatib, Wassim
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Bejoy, Brian
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Lory, Philippe
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Monteil, Arnaud
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3 November 2025
Senatore, Adriano
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Mayorova, Tatiana D.
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Yañez-Guerra, Luis A.
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Elkhatib, Wassim
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Bejoy, Brian
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Lory, Philippe
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Monteil, Arnaud
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Senatore, Adriano, Mayorova, Tatiana D., Yañez-Guerra, Luis A., Elkhatib, Wassim, Bejoy, Brian, Lory, Philippe and Monteil, Arnaud
(2025)
NALCN/Cch1 channelosome subunits originated in early eukaryotes.
The Journal of General Physiology, 157 (6), [e202413636].
(doi:10.1085/jgp.202413636).
Abstract
The sodium leak channel NALCN, a key regulator of neuronal excitability, associates with three ancillary subunits that are critical for its function: a subunit called FAM155, which interacts with the extracellular regions of the channel, and two cytoplasmic subunits called UNC79 and UNC80. Interestingly, NALCN and FAM155 have orthologous phylogenetic relationships with the fungal calcium channel Cch1 and its subunit Mid1; however, UNC79 and UNC80 have not been reported outside of animals. In this study, we leveraged expanded gene sequence data available for eukaryotes to reexamine the evolutionary origins of NALCN and Cch1 channel subunits. Our analysis corroborates the direct phylogenetic relationship between NALCN and Cch1 and identifies a larger clade of related channels in additional eukaryotic taxa. We also identify homologues of FAM155/Mid1 in Cryptista algae and UNC79 and UNC80 homologues in numerous non-metazoan eukaryotes, including basidiomycete and mucoromycete fungi and the microbial eukaryotic taxa Apusomonadida, Malawimonadida, and Discoba. Furthermore, we find that most major animal lineages, except ctenophores, possess a full complement of NALCN subunits. Comparing structural predictions with the solved structure of the human NALCN complex supports orthologous relationships between metazoan and non-metazoan FAM155/Mid1, UNC79, and UNC80 homologues. Together, our analyses reveal unexpected diversity and ancient eukaryotic origins of NALCN/Cch1 channelosome subunits and raise interesting questions about the functional nature of this channel complex within a broad, eukaryotic context.
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jgp_202413636
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Accepted/In Press date: 16 August 2025
e-pub ahead of print date: 5 September 2025
Published date: 3 November 2025
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© 2025 Senatore et al.
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Local EPrints ID: 506211
URI: http://eprints.soton.ac.uk/id/eprint/506211
ISSN: 0022-1295
PURE UUID: 8c53504d-de88-427d-8c08-c9b21714564a
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Date deposited: 30 Oct 2025 17:39
Last modified: 31 Oct 2025 03:05
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Author:
Adriano Senatore
Author:
Tatiana D. Mayorova
Author:
Luis A. Yañez-Guerra
Author:
Wassim Elkhatib
Author:
Brian Bejoy
Author:
Philippe Lory
Author:
Arnaud Monteil
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