4.4 Article

Serotonin signals through postsynaptic Gαq, Trio RhoGEF, and diacylglycerol to promote Caenorhabditis elegans egg-laying circuit activity and behavior

Journal

GENETICS
Volume 221, Issue 3, Pages -

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1093/genetics/iyac084

Keywords

serotonin; Caenorhabditis elegans; neurotransmission; G protein; synapse; circuit activity; optogenetics; calcium imaging; Trio RhoGEF; DAG

Funding

  1. National Institutes of Health [R01-NS086932]
  2. National Science Foundation [IOS-1844657]
  3. American Heart Association [20PRE35210233]
  4. National Institutes of Health Office of Research Infrastructure Programs [P40-OD010440]

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The study demonstrates the essential roles of phospholipase-C beta and Trio Rho GTPase exchange factor in the egg-laying behavior of Caenorhabditis elegans, coordinating cellular responses to neurotransmitter signals by regulating neurotransmitter release and postsynaptic muscle excitability.
Activated G alpha(q) signals through phospholipase-C beta and Trio, a Rho GTPase exchange factor (RhoGEF), but how these distinct effector pathways promote cellular responses to neurotransmitters like serotonin remains poorly understood. We used the egg-laying behavior circuit of Caenorhabditis elegans to determine whether phospholipase-C beta and Trio mediate serotonin and G alpha(q) signaling through independent or related biochemical pathways. Our genetic rescue experiments suggest that phospholipase-C beta functions in neurons while Trio Rho GTPase exchange factor functions in both neurons and the postsynaptic vulval muscles. While G alpha(q), phospholipase-C beta, and Trio Rho GTPase exchange factor mutants fail to lay eggs in response to serotonin, optogenetic stimulation of the serotonin-releasing HSN neurons restores egg laying only in phospholipase-C beta mutants. Phospholipase-C beta mutants showed vulval muscle Ca2+ transients while strong G alpha(q) and Trio Rho GTPase exchange factor mutants had little or no vulval muscle Ca2+ activity. Treatment with phorbol 12-myristate 13-acetate that mimics 1,2-diacylglycerol, a product of PIP2 hydrolysis, rescued egg-laying circuit activity and behavior defects of G alpha(q) signaling mutants, suggesting both phospholipase-C and Rho signaling promote synaptic transmission and egg laying via modulation of 1,2-diacylglycerol levels. 1,2-Diacylglycerol activates effectors including UNC-13; however, we find that phorbol esters, but not serotonin, stimulate egg laying in unc-13 and phospholipase-C beta mutants. These results support a model where serotonin signaling through G alpha(q), phospholipase-C beta, and UNC-13 promotes neurotransmitter release, and that serotonin also signals through G alpha(q), Trio Rho GTPase exchange factor, and an unidentified, phorbol 12-myristate 13-acetate-responsive effector to promote postsynaptic muscle excitability. Thus, the same neuromodulator serotonin can signal in distinct cells and effector pathways to coordinate activation of a motor behavior circuit.

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