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G protein-coupled receptor-based thermosensation determines temperature acclimatization of Caenorhabditis elegans

Kohei Ohnishi, Takaaki Sokabe, Toru Miura, Makoto Tominaga, Akane Ohta, Atsushi Kuhara

2024Nature Communications22 citationsDOIOpen Access PDF

Abstract

Abstract Animals must sense and acclimatize to environmental temperatures for survival, yet their thermosensing mechanisms other than transient receptor potential (TRP) channels remain poorly understood. We identify a trimeric G protein-coupled receptor (GPCR), SRH-40, which confers thermosensitivity in sensory neurons regulating temperature acclimatization in Caenorhabditis elegans . Systematic knockdown of 1000 GPCRs by RNAi reveals GPCRs involved in temperature acclimatization, among which srh-40 is highly expressed in the ADL sensory neuron, a temperature-responsive chemosensory neuron, where TRP channels act as accessorial thermoreceptors. In vivo Ca 2+ imaging demonstrates that an srh-40 mutation reduced the temperature sensitivity of ADL, resulting in supranormal temperature acclimatization. Ectopically expressing SRH-40 in a non-warmth-sensing gustatory neuron confers temperature responses. Moreover, temperature-dependent SRH-40 activation is reconstituted in Drosophila S2R+ cells. Overall, SRH-40 may be involved in thermosensory signaling underlying temperature acclimatization. We propose a dual thermosensing machinery through a GPCR and TRP channels in a single sensory neuron.

Topics & Concepts

Caenorhabditis elegansG protein-coupled receptorAcclimatizationThermoreceptorTransient receptor potential channelSensory neuronCell biologyReceptorNeuronBiologySensory systemGene knockdownNeuroscienceSignal transductionEcologyBiochemistryGeneGenetics, Aging, and Longevity in Model OrganismsCircadian rhythm and melatoninNeurobiology and Insect Physiology Research
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