Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory cilia
| Autor: | Martin Wojtyniak, Piali Sengupta, Andrea G. Brear, Jason Yoon |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Cell signaling
Sensory Receptor Cells Cilium Molecular Sequence Data Context (language use) Tubby protein Biology Investigations biology.organism_classification Cell biology Conserved sequence Receptors G-Protein-Coupled Genetics Animals Amino Acid Sequence Cilia Signal transduction Caenorhabditis elegans Caenorhabditis elegans Proteins hormones hormone substitutes and hormone antagonists Conserved Sequence G protein-coupled receptor Signal Transduction |
| Zdroj: | Genetics. 197(2) |
| ISSN: | 1943-2631 |
| Popis: | The localization of signaling molecules such as G protein-coupled receptors (GPCRs) to primary cilia is essential for correct signal transduction. Detailed studies over the past decade have begun to elucidate the diverse sequences and trafficking mechanisms that sort and transport GPCRs to the ciliary compartment. However, a systematic analysis of the pathways required for ciliary targeting of multiple GPCRs in different cell types in vivo has not been reported. Here we describe the sequences and proteins required to localize GPCRs to the cilia of the AWB and ASK sensory neuron types in Caenorhabditis elegans. We find that GPCRs expressed in AWB or ASK utilize conserved and novel sequences for ciliary localization, and that the requirement for a ciliary targeting sequence in a given GPCR is different in different neuron types. Consistent with the presence of multiple ciliary targeting sequences, we identify diverse proteins required for ciliary localization of individual GPCRs in AWB and ASK. In particular, we show that the TUB-1 Tubby protein is required for ciliary localization of a subset of GPCRs, implying that defects in GPCR localization may be causal to the metabolic phenotypes of tub-1 mutants. Together, our results describe a remarkable complexity of mechanisms that act in a protein- and cell-specific manner to localize GPCRs to cilia, and suggest that this diversity allows for precise regulation of GPCR-mediated signaling as a function of external and internal context. |
| Databáze: | OpenAIRE |
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