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Natural Variation in a Dendritic Scaffold Protein Remodels Experience-Dependent Plasticity by Altering Neuropeptide Expression

The extent to which behavior is shaped by experience varies between individuals. Genetic differences contribute to this variation, but the neural mechanisms are not understood. Here, we dissect natural variation in the behavioral flexibility of two Caenorhabditis elegans wild strains. In one strain,...

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Detalles Bibliográficos
Autores principales: Beets, Isabel, Zhang, Gaotian, Fenk, Lorenz A., Chen, Changchun, Nelson, Geoffrey M., Félix, Marie-Anne, de Bono, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953435/
https://www.ncbi.nlm.nih.gov/pubmed/31757604
http://dx.doi.org/10.1016/j.neuron.2019.10.001
Descripción
Sumario:The extent to which behavior is shaped by experience varies between individuals. Genetic differences contribute to this variation, but the neural mechanisms are not understood. Here, we dissect natural variation in the behavioral flexibility of two Caenorhabditis elegans wild strains. In one strain, a memory of exposure to 21% O(2) suppresses CO(2)-evoked locomotory arousal; in the other, CO(2) evokes arousal regardless of previous O(2) experience. We map that variation to a polymorphic dendritic scaffold protein, ARCP-1, expressed in sensory neurons. ARCP-1 binds the Ca(2+)-dependent phosphodiesterase PDE-1 and co-localizes PDE-1 with molecular sensors for CO(2) at dendritic ends. Reducing ARCP-1 or PDE-1 activity promotes CO(2) escape by altering neuropeptide expression in the BAG CO(2) sensors. Variation in ARCP-1 alters behavioral plasticity in multiple paradigms. Our findings are reminiscent of genetic accommodation, an evolutionary process by which phenotypic flexibility in response to environmental variation is reset by genetic change.