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Specification of muscle neurotransmitter sensitivity by a Paired-like homeodomain protein in Caenorhabditis elegans
Robyn Branicky1, Siegfried Hekimi
1Department of Biology, McGill University, 1205 Avenue Dr Penfield, Montréal, Québec H3A 1B1, Canada.
Abstract:
The effects of neurotransmitters depend on the receptors expressed on the target cells. In Caenorhabditis elegans, there are two types of GABA receptors that elicit opposite effects: excitatory receptors that open cation-selective channels, and inhibitory receptors that open anion-selective channels. The four non-striated enteric muscle cells required for the expulsion step of the defecation behavior are all sensitive to GABA: the sphincter muscle expresses a classical GABA-sensitive chloride channel (UNC-49) and probably relaxes in response to GABA, while the other three cells express a cation-selective channel (EXP-1) and contract. Here we show that the expression of the exp-1 gene is under the control of dsc-1, which encodes a Paired-like homeodomain protein, a class of transcription factors previously associated with the terminal differentiation of neurons in C. elegans. dsc-1 mutants have anatomically normal enteric muscles but are expulsion defective. We show that this defect is due to the lack of expression of exp-1 in the three cells that contract in response to GABA. In addition, dsc-1, but not exp-1, affects the periodicity of the behavior, revealing an unanticipated role for the enteric muscles in regulating this ultradian rhythm.
Insights
The transcription factor DSC-1 regulates GABA-gated cation channels (EXP-1) in C. elegans enteric muscles, controlling defecation expulsion. DSC-1 also influences the rhythm of this behavior, suggesting a novel role for enteric muscles in ultradian rhythm regulation.
Area of Science:
- Neuroscience
- Developmental Biology
- Genetics
Background:
- Neurotransmitter effects are receptor-dependent, with GABA receptors mediating excitation or inhibition.
- In C. elegans, enteric muscles use GABA-gated channels (UNC-49 for inhibition, EXP-1 for excitation) for defecation expulsion.
Purpose of the Study:
- To investigate the genetic control of EXP-1 expression in C. elegans enteric muscles.
- To elucidate the role of DSC-1 in regulating defecation behavior and its periodicity.
Main Methods:
- Gene expression analysis of exp-1 in dsc-1 mutants.
- Phenotypic analysis of defecation behavior in mutant C. elegans strains.
- Assessment of exp-1 and dsc-1 roles in behavioral periodicity.
Main Results:
- The transcription factor DSC-1 controls the expression of the cation channel EXP-1 in specific enteric muscle cells.
- dsc-1 mutants exhibit defective defecation expulsion due to lack of EXP-1 expression.
- DSC-1, but not EXP-1, influences the periodicity of the defecation rhythm.
Conclusions:
- DSC-1 is a key regulator of excitatory GABA receptor expression in enteric muscles.
- Enteric muscles play an unexpected role in modulating ultradian rhythms through DSC-1.
- This study reveals a novel link between transcription factors, muscle function, and behavioral timing.

