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Journal of NeuroscienceNeurosciencePeer-reviewed journal article

Loss of CaMKI function disrupts salt aversive learning in C. elegans

Jana P. LimiD, Holger Fehlauer, Alakananda DasiD, Gabriella SaròiD, Dominique A. GlauseriD, Anne BrunetiD, Miriam B. GoodmaniD

PDFDOIPreprint

Abstract

The ability to adapt behavior to environmental fluctuations is critical for survival of organisms ranging from invertebrates to mammals. Caenorhabditis elegans can learn to avoid sodium chloride when it is paired with starvation. This behavior is likely advantageous to avoid areas without food. While some genes have been implicated in this salt aversive learning behavior, critical genetic components, and the neural circuit in which they act, remain elusive. Here, we show that the sole worm ortholog of mammalian CaMKI/IV, CMK-1, is essential for salt aversive learning behavior in C. elegans. We find that CMK-1 acts in the primary salt-sensing ASE neurons to regulate this behavior. By characterizing the intracellular calcium dynamics in ASE neurons using microfluidics, we find that loss of cmk-1 leads to an altered pattern of sensory-evoked calcium responses that may underlie salt aversive learning. Our study implicates the conserved CaMKI/CMK-1 as an essential cell-autonomous regulator for behavioral plasticity to environmental salt in C. elegans.\n\nSignificance StatementLike other animals, the nematode Caenorhabditis elegans depends on salt for survival and navigates toward high concentrations of this essential mineral. Because salt generates osmotic stress at high concentrations, it also threatens the survival of small terrestrial animals like C. elegans. A growing body of evidence indicates that C. elegans balances these factors through a process called salt aversive learning. We show that this behavior depends on expression of a calcium/calmodulin-dependent kinase, CMK-1, in the ASE salt sensing neurons and that salt-induced calcium signals in the ASE neurons are less sensitive to salt conditioning in animals lacking CMK-1 function. Our study identifies CMK-1 and sensory neurons as key factors in this form of behavioral plasticity.

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