Parallel Erosion of a Testis-Specific Na+/K+ ATPase in Three Mammalian Lineages Sheds Light into the Evolution of Spermatozoa Energetics.

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Main Authors: Valente, Raul, Machado, André M, Pericuesta, Eva, García-Párraga, Daniel, Artilheiro, Nádia, Alves, Filipe, Sousa-Pinto, Isabel, Pinto, Bernardo, Cordeiro, J Miguel, Ruivo, Raquel, Gutiérrez-Adán, Alfonso, Castro, L Filipe C
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Language:en
Published: Genome biology and evolution 2026
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author Valente, Raul
Machado, André M
Pericuesta, Eva
García-Párraga, Daniel
Artilheiro, Nádia
Alves, Filipe
Sousa-Pinto, Isabel
Pinto, Bernardo
Cordeiro, J Miguel
Ruivo, Raquel
Gutiérrez-Adán, Alfonso
Castro, L Filipe C
author_facet Valente, Raul
Machado, André M
Pericuesta, Eva
García-Párraga, Daniel
Artilheiro, Nádia
Alves, Filipe
Sousa-Pinto, Isabel
Pinto, Bernardo
Cordeiro, J Miguel
Ruivo, Raquel
Gutiérrez-Adán, Alfonso
Castro, L Filipe C
Valente, Raul
Machado, André M
Pericuesta, Eva
García-Párraga, Daniel
Artilheiro, Nádia
Alves, Filipe
Sousa-Pinto, Isabel
Pinto, Bernardo
Cordeiro, J Miguel
Ruivo, Raquel
Gutiérrez-Adán, Alfonso
Castro, L Filipe C
collection PubMed - marine biology
contents Parallel Erosion of a Testis-Specific Na+/K+ ATPase in Three Mammalian Lineages Sheds Light into the Evolution of Spermatozoa Energetics. Valente, Raul Machado, André M Pericuesta, Eva García-Párraga, Daniel Artilheiro, Nádia Alves, Filipe Sousa-Pinto, Isabel Pinto, Bernardo Cordeiro, J Miguel Ruivo, Raquel Gutiérrez-Adán, Alfonso Castro, L Filipe C Animals Male Sodium-Potassium-Exchanging ATPase Spermatozoa Testis Evolution, Molecular Energy Metabolism Gene Duplication Phylogeny Mammals Understanding how extant physiological landscapes arise from novel genetic interactions is key to elucidating phenotypic evolution. Sperm cells exemplify a striking case of functional compartmentalization shaped by molecular adjustments, notably regarding energy metabolism. Here, we examine the impact of gene duplication and loss on the evolution of sperm energetics in mammals. Our findings reveal that the acquisition of an exclusive mechanism controlling the sperm plasma membrane Na+ gradient, critical for glucose uptake, emerged in the ancestor of mammals through gene duplication, which originated the Na+/K+ ATPase transporting subunit alpha 4 transporter (Atp1a4). Furthermore, we demonstrate that testis-specific expression of Atp1a4 was acquired after the divergence from monotremes. Notably, we identify three independent pseudogenization events of Atp1a4, including in pangolins, the naked mole-rat (Heterocephalus glaber) and toothed whales. The recurrent loss of function in Atp1a4 coincides with the erosion of the testis-specific glycolytic pathway in these lineages. Furthermore, enrichment analysis of striped dolphin (Stenella coeruleoalba) and naked mole-rat testis transcriptomes also suggests significant alterations in sperm capacitation processes. Overall, we show that the elaboration of a sodium-dependent glucose uptake wiring was a key innovation in the energetic landscape governing mammalian spermatozoa, with secondary gene loss in three separate lineages pointing to drastic alterations in motility and capacitation processes. Our findings illustrate how metabolic pathways co-shaped by gene duplication and erosion define extant physiological phenotypes.
format Artículo científico
id pubmed_41626717
institution PubMed
language en
publishDate 2026
publisher Genome biology and evolution
record_format pubmed
spellingShingle Parallel Erosion of a Testis-Specific Na+/K+ ATPase in Three Mammalian Lineages Sheds Light into the Evolution of Spermatozoa Energetics.
Valente, Raul
Machado, André M
Pericuesta, Eva
García-Párraga, Daniel
Artilheiro, Nádia
Alves, Filipe
Sousa-Pinto, Isabel
Pinto, Bernardo
Cordeiro, J Miguel
Ruivo, Raquel
Gutiérrez-Adán, Alfonso
Castro, L Filipe C
Animals
Male
Sodium-Potassium-Exchanging ATPase
Spermatozoa
Testis
Evolution, Molecular
Energy Metabolism
Gene Duplication
Phylogeny
Mammals
Parallel Erosion of a Testis-Specific Na+/K+ ATPase in Three Mammalian Lineages Sheds Light into the Evolution of Spermatozoa Energetics. Valente, Raul Machado, André M Pericuesta, Eva García-Párraga, Daniel Artilheiro, Nádia Alves, Filipe Sousa-Pinto, Isabel Pinto, Bernardo Cordeiro, J Miguel Ruivo, Raquel Gutiérrez-Adán, Alfonso Castro, L Filipe C Animals Male Sodium-Potassium-Exchanging ATPase Spermatozoa Testis Evolution, Molecular Energy Metabolism Gene Duplication Phylogeny Mammals Understanding how extant physiological landscapes arise from novel genetic interactions is key to elucidating phenotypic evolution. Sperm cells exemplify a striking case of functional compartmentalization shaped by molecular adjustments, notably regarding energy metabolism. Here, we examine the impact of gene duplication and loss on the evolution of sperm energetics in mammals. Our findings reveal that the acquisition of an exclusive mechanism controlling the sperm plasma membrane Na+ gradient, critical for glucose uptake, emerged in the ancestor of mammals through gene duplication, which originated the Na+/K+ ATPase transporting subunit alpha 4 transporter (Atp1a4). Furthermore, we demonstrate that testis-specific expression of Atp1a4 was acquired after the divergence from monotremes. Notably, we identify three independent pseudogenization events of Atp1a4, including in pangolins, the naked mole-rat (Heterocephalus glaber) and toothed whales. The recurrent loss of function in Atp1a4 coincides with the erosion of the testis-specific glycolytic pathway in these lineages. Furthermore, enrichment analysis of striped dolphin (Stenella coeruleoalba) and naked mole-rat testis transcriptomes also suggests significant alterations in sperm capacitation processes. Overall, we show that the elaboration of a sodium-dependent glucose uptake wiring was a key innovation in the energetic landscape governing mammalian spermatozoa, with secondary gene loss in three separate lineages pointing to drastic alterations in motility and capacitation processes. Our findings illustrate how metabolic pathways co-shaped by gene duplication and erosion define extant physiological phenotypes.
title Parallel Erosion of a Testis-Specific Na+/K+ ATPase in Three Mammalian Lineages Sheds Light into the Evolution of Spermatozoa Energetics.
topic Animals
Male
Sodium-Potassium-Exchanging ATPase
Spermatozoa
Testis
Evolution, Molecular
Energy Metabolism
Gene Duplication
Phylogeny
Mammals
url https://pubmed.ncbi.nlm.nih.gov/41626717/