gcy-18

UniProt ID: G5EFQ0
Organism: Caenorhabditis elegans
Review Status: COMPLETE
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Gene Description

gcy-18 encodes a receptor-type (transmembrane) guanylate cyclase expressed exclusively in the AFD thermosensory neurons of C. elegans. With GCY-8, GCY-18 and GCY-23 it forms an AFD-specific subfamily; each has an extracellular domain with little similarity to mammalian receptor guanylyl cyclases, a single transmembrane helix, an intracellular kinase-homology domain predicted to be catalytically inactive, and a C-terminal guanylate cyclase domain that converts GTP to cGMP. GCY-18 is concentrated at the AFD sensory ending (the microvillar receptive ending). The three AFD cyclases act partly redundantly to supply the cGMP that opens the TAX-2/TAX-4 cyclic nucleotide-gated channel in response to warming; triple mutants are athermotactic and lack temperature-evoked AFD currents. GCY-18 acts as the primary AFD cyclase at higher cultivation temperatures; gcy-18 mutants still track isotherms but in a range shifted toward colder temperatures, and their AFD neurons have a lowered temperature response threshold, indicating that GCY-18 sets the operating range of thermosensation.

Existing Annotations Review

GO Term Evidence Action Reason
GO:0001653 peptide receptor activity
IBA
GO_REF:0000033
MARK AS OVER ANNOTATED
Summary: PANTHER IBA transfer of peptide receptor activity from vertebrate natriuretic peptide receptor guanylyl cyclases.
Reason: GCY-18 is an AFD-specific receptor guanylyl cyclase of the GCY-8/18/23 subfamily whose extracellular domain shows little homology to human guanylyl cyclases; no peptide ligand is known. The only identified extracellular regulator of this subfamily is inhibitory chloride acting on GCY-8. Peptide-receptor activity is a natriuretic-peptide-receptor-specific property not demonstrated for this nematode clade.
Propagation Review
Root cause: PROPAGATION BAD
Failure modes: FUNCTIONAL DIVERGENCE
Sources checked:
PANTHER:PTN000229249 SUPPORTS SOURCE BUT NOT TARGET
Peptide-receptor activity is grounded in vertebrate natriuretic peptide receptor guanylyl cyclases (NPR-A/NPR-B); the C. elegans sensory receptor guanylyl cyclase radiation has no demonstrated peptide ligand.
Supporting Evidence:
PMID:16415369
GCY-8, -18, and -23 showed little homology to human guanylyl cyclases in the extracellular domain
GO:0004383 guanylate cyclase activity
IBA
GO_REF:0000033
ACCEPT
Summary: IBA guanylate cyclase activity; GCY-18 has a conserved C-terminal class-4 guanylate cyclase domain and belongs to the receptor guanylyl cyclase clade. Core.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
GO:0004383 guanylate cyclase activity
IEA
GO_REF:0000120
ACCEPT
Summary: Combined automated (EC 4.6.1.2/RHEA) guanylate cyclase activity, consistent with domain architecture. Core.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
GO:0004383 guanylate cyclase activity
ISS
GO_REF:0000024
ACCEPT
Summary: ISS (curator judgment of sequence similarity) guanylate cyclase activity, consistent with the conserved cyclase domain and the redundant cGMP-producing role of the AFD GCY subfamily. Core.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0004383 guanylate cyclase activity
ISS
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: ISS guanylate cyclase activity from the paper identifying the AFD GCY-8/18/23 subfamily, which proposes that these cyclases transduce temperature into cGMP for the TAX-4 channel. Core.
Supporting Evidence:
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0004672 protein kinase activity
IEA
GO_REF:0000002
REMOVE
Summary: InterPro mapping from the kinase-homology domain to protein kinase activity.
Reason: In receptor guanylyl cyclases the kinase-homology domain is a regulatory pseudokinase; UniProt states the GCY-18 kinase domain is predicted to be catalytically inactive, and no kinase activity has been reported. The InterPro2GO mapping for the Ser/Thr/Tyr kinase domain is not applicable to this pseudokinase.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
The protein kinase domain is predicted to be catalytically inactive.
GO:0005524 ATP binding
IEA
GO_REF:0000002
KEEP AS NON CORE
Summary: InterPro ATP binding from the kinase-homology domain. The pseudokinase domain of receptor guanylyl cyclases may bind ATP as a regulator of cyclase activity, but this is untested here. Non-core.
Supporting Evidence:
PMID:16415369
Three serine and threonine residues that have been reported to be reversibly phosphorylated in mammalian guanylyl cyclases were also conserved in the kinase homology domains of the GCY-8, GCY-18, and GCY-23 guanylyl cyclases.
GO:0005886 plasma membrane
IBA
GO_REF:0000033
KEEP AS NON CORE
Summary: GCY-18 is a single-pass type I membrane protein; plasma membrane is correct, but the functional pool is in the AFD sensory ending (microvilli) membrane.
Supporting Evidence:
PMID:16415369
GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD
GO:0005886 plasma membrane
IEA
GO_REF:0000044
KEEP AS NON CORE
Summary: UniProt subcellular-location mapping (cell membrane). Correct but less specific than the AFD sensory-ending localization.
Supporting Evidence:
PMID:16415369
GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD
IEA
GO_REF:0000044
KEEP AS NON CORE
Summary: UniProt subcellular-location mapping to cilium, based on localization to the AFD sensory ending.
Reason: The AFD sensory ending comprises a short bona fide cilium plus an elaborate microvillar subcompartment; Nguyen et al. show that the thermosensory guanylyl cyclases are localized to the microvillar compartment (dependent on BBS-8 and DAF-25), whereas the CNG channel is anchored in the proximal cilium. Cilium is therefore an approximation of the true location; retained as non-core.
Supporting Evidence:
PMID:16415369
GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD
PMID:25335890
requires BBS-8 and DAF-25 (known as Ankmy2 in mammals) for correct localization of guanylyl cyclases needed for thermosensation
GO:0006182 cGMP biosynthetic process
IBA
GO_REF:0000033
ACCEPT
Summary: cGMP biosynthesis is the direct process of the cyclase activity, providing cGMP for the TAX-2/TAX-4 channel in AFD. Core.
Supporting Evidence:
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0007168 receptor guanylyl cyclase signaling pathway
IBA
GO_REF:0000033
ACCEPT
Summary: Receptor guanylyl cyclase signaling pathway (IBA). Pathway-level term appropriate for an AFD rGC feeding cGMP to TAX-4; the activating stimulus (temperature, possibly directly) is not a classical ligand.
Supporting Evidence:
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0007168 receptor guanylyl cyclase signaling pathway
ISS
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: ISS receptor guanylyl cyclase signaling pathway, same rationale as the IBA.
Supporting Evidence:
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0009190 cyclic nucleotide biosynthetic process
IEA
GO_REF:0000002
KEEP AS NON CORE
Summary: InterPro-derived parent of cGMP biosynthetic process. Correct but less specific.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
GO:0016048 detection of temperature stimulus
IEA
GO_REF:0000117
ACCEPT
Summary: ARBA detection of temperature stimulus; consistent with the role of the AFD rGCs in converting temperature into a cGMP signal.
Supporting Evidence:
PMID:16415369
Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
GO:0016048 detection of temperature stimulus
IGI
PMID:21315599
Regulation of response properties and operating range of the...
ACCEPT
Summary: Triple gcy mutants fail to exhibit temperature-induced currents in AFD, showing the rGCs are required to convert a thermal stimulus into a cellular signal. Core.
Supporting Evidence:
PMID:21315599
Animals mutant for the TAX-2 and TAX-4 cGMP-gated channels, or triply mutant for the GCY-8, GCY-18 and GCY-23 receptor guanylyl cyclases (rGCs) are atactic, and fail to exhibit temperature-induced currents in the AFD neurons
GO:0016048 detection of temperature stimulus
IMP
PMID:21315599
Regulation of response properties and operating range of the...
ACCEPT
Summary: gcy-18 single mutants show a significantly lowered AFD temperature response threshold (T*AFD) at 20Β°C, paralleling their shifted thermotactic operating range; GCY-18 therefore contributes to temperature detection by AFD. Core.
Supporting Evidence:
PMID:21315599
Consistent with a larger downward shift in Tc memory of gcy-18 mutants grown at 20Β°C, the T*AFD in their AFD neurons was also significantly lower
GO:0016849 phosphorus-oxygen lyase activity
IEA
GO_REF:0000002
KEEP AS NON CORE
Summary: InterPro-derived phosphorus-oxygen lyase activity, the parent class of guanylate cyclase activity (EC 4.6.1). Correct but less specific.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
GO:0031528 microvillus membrane
IDA
PMID:25335890
Ciliopathy proteins establish a bipartite signaling compartm...
ACCEPT
Summary: The AFD thermosensory guanylyl cyclases localize to the microvillar subcompartment of the AFD sensory ending, which requires BBS-8 and DAF-25 for their correct localization (IDA in full text). Precise core location.
Supporting Evidence:
PMID:25335890
requires BBS-8 and DAF-25 (known as Ankmy2 in mammals) for correct localization of guanylyl cyclases needed for thermosensation
GO:0035556 intracellular signal transduction
IEA
GO_REF:0000002
KEEP AS NON CORE
Summary: InterPro-derived intracellular signal transduction; correct (cGMP second messenger) but uninformative.
Supporting Evidence:
file:worm/gcy-18/gcy-18-uniprot.txt
Guanylate cyclase involved in the production of the second messenger cGMP
GO:0040040 thermosensory behavior
IEA
GO_REF:0000117
ACCEPT
Summary: ARBA thermosensory behavior; consistent with experimental data.
Supporting Evidence:
PMID:16415369
gcy-23 gcy-8 gcy-18 triple mutants show a cryophilic or athermotactic phenotype (no response to temperature) similar to the phenotype of AFD-killed wild-type animals.
GO:0040040 thermosensory behavior
IGI
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: Double/triple gcy mutants are cryophilic or athermotactic, and any single GCY rescues the triple mutant: the three AFD rGCs act redundantly in thermosensory behavior. Core.
Supporting Evidence:
PMID:16415369
gcy-23 gcy-8 gcy-18 triple mutants show a cryophilic or athermotactic phenotype (no response to temperature) similar to the phenotype of AFD-killed wild-type animals.
PMID:16415369
The thermotaxis mutant phenotype of the gcy triple-mutant strain was rescued by expression of any one of the three GCY proteins, suggesting that the GCY-8, -18, and -23 guanylyl cyclases function redundantly
GO:0040040 thermosensory behavior
IGI
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: Double/triple gcy mutants are cryophilic or athermotactic, and any single GCY rescues the triple mutant: the three AFD rGCs act redundantly in thermosensory behavior. Core.
Supporting Evidence:
PMID:16415369
gcy-23 gcy-8 gcy-18 triple mutants show a cryophilic or athermotactic phenotype (no response to temperature) similar to the phenotype of AFD-killed wild-type animals.
PMID:16415369
The thermotaxis mutant phenotype of the gcy triple-mutant strain was rescued by expression of any one of the three GCY proteins, suggesting that the GCY-8, -18, and -23 guanylyl cyclases function redundantly
GO:0040040 thermosensory behavior
IGI
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: Double/triple gcy mutants are cryophilic or athermotactic, and any single GCY rescues the triple mutant: the three AFD rGCs act redundantly in thermosensory behavior. Core.
Supporting Evidence:
PMID:16415369
gcy-23 gcy-8 gcy-18 triple mutants show a cryophilic or athermotactic phenotype (no response to temperature) similar to the phenotype of AFD-killed wild-type animals.
PMID:16415369
The thermotaxis mutant phenotype of the gcy triple-mutant strain was rescued by expression of any one of the three GCY proteins, suggesting that the GCY-8, -18, and -23 guanylyl cyclases function redundantly
GO:0040040 thermosensory behavior
IGI
PMID:21315599
Regulation of response properties and operating range of the...
ACCEPT
Summary: Triple gcy mutants are atactic and lack temperature-induced AFD currents (IGI). Core.
Supporting Evidence:
PMID:21315599
Animals mutant for the TAX-2 and TAX-4 cGMP-gated channels, or triply mutant for the GCY-8, GCY-18 and GCY-23 receptor guanylyl cyclases (rGCs) are atactic, and fail to exhibit temperature-induced currents in the AFD neurons
GO:0043052 thermotaxis
IEA
GO_REF:0000117
ACCEPT
Summary: ARBA thermotaxis; consistent with experimental data.
Supporting Evidence:
PMID:16415369
gcy-23 gcy-8 gcy-18 triple mutants show a cryophilic or athermotactic phenotype (no response to temperature) similar to the phenotype of AFD-killed wild-type animals.
GO:0043052 thermotaxis
IGI
PMID:21315599
Regulation of response properties and operating range of the...
ACCEPT
Summary: Genetic interaction data showing the AFD rGCs jointly required for thermotaxis/isothermal tracking. Core.
Supporting Evidence:
PMID:21315599
Animals mutant for the TAX-2 and TAX-4 cGMP-gated channels, or triply mutant for the GCY-8, GCY-18 and GCY-23 receptor guanylyl cyclases (rGCs) are atactic, and fail to exhibit temperature-induced currents in the AFD neurons
PMID:21315599
Thus, while all three rGC genes play roles in regulating the temperature range in which IT behavior can be exhibited, only gcy-8 regulates the ability of the AFD neurons to execute IT behavior.
GO:0044306 neuron projection terminus
IDA
PMID:16415369
Identification of guanylyl cyclases that function in thermos...
ACCEPT
Summary: GFP-tagged GCY-18 is localized exclusively to the AFD sensory ending (dendritic terminus). Correct and reasonably specific; microvillus membrane is the more precise compartment.
Supporting Evidence:
PMID:16415369
GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD
GO:0044306 neuron projection terminus
IEA
GO_REF:0000117
ACCEPT
Summary: ARBA neuron projection terminus; matches the experimental sensory-ending localization.
Supporting Evidence:
PMID:16415369
GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD

Core Functions

AFD-specific receptor guanylate cyclase: converts GTP to cGMP at the AFD sensory ending, supplying the cGMP that gates the TAX-2/TAX-4 channel in thermotransduction (partly redundant with the other AFD GCYs).

Supporting Evidence:
  • PMID:16415369
    GFP-tagged GCY-8, 18, and 23 were localized exclusively to the sensory endings of AFD
  • PMID:16415369
    Temperature received by a thermoreceptor is transduced to changes in intracellular cGMP concentration via three guanylyl cyclases, GCY-8, GCY-18, and GCY-23, and transmitted to the TAX-4 CNG channel, resulting in a change of membrane potential of AFD.
  • PMID:16415369
    The thermotaxis mutant phenotype of the gcy triple-mutant strain was rescued by expression of any one of the three GCY proteins, suggesting that the GCY-8, -18, and -23 guanylyl cyclases function redundantly

Sets the temperature operating range (cultivation-temperature memory) of AFD-mediated isothermal tracking; principal AFD cyclase at 20-25Β°C.

Molecular Function:
guanylate cyclase activity
Directly Involved In:
Supporting Evidence:
  • PMID:21315599
    These results imply that while GCY-18 and GCY-23 are not essential for the execution of IT behavior, these rGCs play important roles in setting Tc memory.
  • PMID:21315599
    Consistent with a larger downward shift in Tc memory of gcy-18 mutants grown at 20Β°C, the T*AFD in their AFD neurons was also significantly lower
  • PMID:16415369
    suggesting that gcy-18 functions as the primary guanylyl cyclase in these temperature ranges

References

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Suggested Questions for Experts

Q: Are the AFD receptor guanylyl cyclases intrinsically thermosensitive (i.e. the thermoreceptors themselves), and which domain confers temperature dependence of cyclase activity?

Suggested Experiments

Experiment: Express each AFD rGC (GCY-8, GCY-18, GCY-23) alone in a heterologous cell with a cGMP sensor and measure temperature-dependent cGMP production, swapping extracellular and kinase-homology domains to map thermosensitivity.

Deep Research

WormBase

(gcy-18-deep-research-wormbase.md)

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πŸ“š Additional Documentation

Notes

(gcy-18-notes.md)

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