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Updated: Jul 2, 2026

Paradigms for Pharmacological Characterization of C. elegans Synaptic Transmission Mutants
Published on: August 18, 2008
Immature C. elegans motor neurons control early embryo behavior via both synaptic and non-synaptic GABA release
James Marvel-Coen1,2, Evan Ardiel1,2,3, Jian Zhao1,2
1Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
None:
Pre-natal brain activity has long lasting effects on subsequent neurodevelopment. It is unclear if early brain activity is dominated by cell intrinsic, synaptic, or non-synaptic mechanisms. We address this question by analyzing C. elegans embryo behavior in snf-11 mutants, which lack a plasma membrane GABA re-uptake pump (orthologous to GAT1). At 510-570 minutes post-fertilization, embryo motion was transiently and potently inhibited in snf-11 GAT1 mutants, which precedes formation of most nerve ring synapses. This transient motion inhibition requires GABA synthesis in DD motor neurons and UNC-49 GABAA receptors in body muscles. When motion inhibition occurs, DD neurons have not yet completed neurite outgrowth. Genetic analysis suggests that motion inhibition was mediated by both synaptic and tonic GABA release from DD motor neurons. These results suggest that DD neurons control embryo behavior prior to completing their developmental maturation.
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