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dc.contributor.advisorMark J. Alkema
dc.contributor.authorPirri, Jennifer K.
dc.date2022-08-11T08:08:44.000
dc.date.accessioned2022-08-23T16:06:08Z
dc.date.available2022-08-23T16:06:08Z
dc.date.issued2013-03-28
dc.date.submitted2013-07-22
dc.identifier.doi10.13028/M2GP58
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32015
dc.description<p>This dissertation includes 16 videos that are referenced in Chapters II, III, and IV. See <strong>Additional Files</strong> below.</p>
dc.description.abstractDespite the current understanding that sensorimotor circuits function through the action of transmitters and modulators, we have a limited understanding of how the nervous system directs the flow of information necessary to orchestrate complex behaviors. In this dissertation, I aimed to uncover how the nervous system coordinates these behaviors using the escape response of the soil nematode, Caenorhabditis elegans, as a paradigm. C. elegans exhibits a robust escape behavior in response to touch. The worm typically moves forward in a sinusoidal pattern, which is accompanied by exploratory head movements. During escape, the worm quickly retreats by moving backward from the point of stimulus while suppressing its head movements. It was previously shown that the biogenic amine tyramine played an important role in modulating the suppression of these head movmemetns in response to touch. We identified a novel tyramine-gated chloride channel, LGC-55, whose activation by tyramine coordinates motor programs essential for escape. Furthermore, we found that changing the electrical nature of a synapse within the neural circuit for escape behavior can reverse its behavioral output, indicating that the C. elegans connectome is established independent of the nature of synaptic activity or behavioral output. Finally, we characterized a unique mutant, zf35 , which is hyperactive in reversal behavior. This mutant was identified as a gain of function allele of the C. elegans P/Q/N-type voltage-gated calcium channel, UNC-2. Taken together, this work defines tyramine as a genuine neurotransmitter and completes the neural circuit that controls the initial phases of the C. elegans escape response. Additionally, this research further advances the understanding of how the interactions between transmitters and ion channels can precisely regulate neural circuit activity in the execution of a complex behavior.
dc.language.isoen_US
dc.rightsCopyright is held by the author, with all rights reserved.
dc.subjectDissertations, UMMS
dc.subjectCaenorhabditis elegans
dc.subjectIon Channels
dc.subjectNeurotransmitter Agents
dc.subjectTyramine
dc.subjectEscape Reaction
dc.subjectCaenorhabditis elegans
dc.subjection channels
dc.subjecttransmitters
dc.subjectescape behavior
dc.subjectBehavioral Neurobiology
dc.subjectMolecular and Cellular Neuroscience
dc.titleThe Role of Ion Channels in Coordinating Neural Circuit Activity in Caenorhabditis elegans: A Dissertation
dc.typeDoctoral Dissertation
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1664&amp;context=gsbs_diss&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_diss/662
dc.legacy.embargo2014-04-24T00:00:00-07:00
dc.identifier.contextkey4334857
dc.file.descriptionMovie of a wild-type animal on plates containing 30 mM tyramine.
dc.file.descriptionMovie of a wild-type animal after 5 minutes on plates containing 30 mM tyramine.
dc.file.descriptionMovie of a lgc-55 animal after 5 minutes on plates containing 30 mM tyramine.
dc.file.descriptionMovie of gentle anterior touch response of wild-type animals.
dc.file.descriptionMovie of gentle anterior touch response of lgc-55(tm2913) mutant animals.
dc.file.descriptionMovie of gentle anterior touch response of transgenic animals expressing glr-1::LGC-55.
dc.file.descriptionMovie of gentle anterior touch response of transgenic animals expressing myo-3::LGC-55.
dc.file.descriptionMovie of a wild-type animal on a plate containing 30 mM tyramine.
dc.file.descriptionMovie of LGC-55 LM2 on a plate containing 30 mM tyramine.
dc.file.descriptionMovie of gentle anterior touch response of wild-type animals.
dc.file.descriptionMovie of gentle anterior touch response of LGC-55 LM2 animals.
dc.file.descriptionMovie of wild-type animals expressing ptdc-1::ChR2 in response to blue light.
dc.file.descriptionMovie of LGC-55 LM2 animals expressing ptdc-1::ChR2 in response to blue light.
dc.file.descriptionMovie of wild-type animals on food.
dc.file.descriptionMovie of zf35 animals on food.
dc.file.descriptionMovie of e55 animals on food.
refterms.dateFOA2022-08-23T17:02:07Z
html.description.abstract<p>Despite the current understanding that sensorimotor circuits function through the action of transmitters and modulators, we have a limited understanding of how the nervous system directs the flow of information necessary to orchestrate complex behaviors. In this dissertation, I aimed to uncover how the nervous system coordinates these behaviors using the escape response of the soil nematode, <em>Caenorhabditis elegans</em>, as a paradigm. <em>C. elegans</em> exhibits a robust escape behavior in response to touch. The worm typically moves forward in a sinusoidal pattern, which is accompanied by exploratory head movements. During escape, the worm quickly retreats by moving backward from the point of stimulus while suppressing its head movements. It was previously shown that the biogenic amine tyramine played an important role in modulating the suppression of these head movmemetns in response to touch. We identified a novel tyramine-gated chloride channel, LGC-55, whose activation by tyramine coordinates motor programs essential for escape. Furthermore, we found that changing the electrical nature of a synapse within the neural circuit for escape behavior can reverse its behavioral output, indicating that the <em>C. elegans</em> connectome is established independent of the nature of synaptic activity or behavioral output. Finally, we characterized a unique mutant, <em>zf35</em> , which is hyperactive in reversal behavior. This mutant was identified as a gain of function allele of the <em>C. elegans</em> P/Q/N-type voltage-gated calcium channel, UNC-2. Taken together, this work defines tyramine as a genuine neurotransmitter and completes the neural circuit that controls the initial phases of the <em>C. elegans</em> escape response. Additionally, this research further advances the understanding of how the interactions between transmitters and ion channels can precisely regulate neural circuit activity in the execution of a complex behavior.</p>
dc.identifier.submissionpathgsbs_diss/662
dc.contributor.departmentAlkema Lab
dc.contributor.departmentNeurobiology
dc.description.thesisprogramNeuroscience


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