ArticleCommunications biology2025
Evolution of iGluR ligand specificity, polyamine regulation, and ion selectivity inferred from a placozoan epsilon receptor.
Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Tunable AMPA receptor function via recurrent evolution of heterotetramers.The Journal of general physiology · 2026Article
- The AMPA receptor life cycle: assembly, regulation and synaptic diversity.Nature reviews. Neuroscience · 2026Review
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Authors and funding
10 authors.
Funding
Abstract
Epsilon ionotropic glutamate receptors (iGluRs) are a recently defined clade of neurotransmitter receptors that are found in all major metazoan lineages that are distinct from α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), kainate, delta, phi (i.e., AKDF) and N-methyl-D-aspartate NMDA receptors. Here, we explore the evolution of iGluRs by generating a broad species-guided phylogeny of eukaryotic iGluRs and a comprehensive phylogeny of placozoan receptors, uncovering marked diversification of epsilon type receptors within Placozoa. Functional characterization of one epsilon receptor from the placozoan species Trichoplax adhaerens, named GluE1αA, reveals sensitivity to glycine, alanine, serine, and valine, but not glutamate. We demonstrate that changing just three amino acids in the ligand binding domain could convert ligand specificity of GluE1αA from glycine to glutamate, also causing nascent sensitivity to AMPA and increased sensitivity to the blocker 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX). We also demonstrate that an atypical serine in the pore Q/R/N site confers diminished Ca
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