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dc.contributor.authorBhattacharya, Raja
dc.contributor.authorFrancis, Michael M.
dc.date2022-08-11T08:09:29.000
dc.date.accessioned2022-08-23T16:32:37Z
dc.date.available2022-08-23T16:32:37Z
dc.date.issued2015-07-09
dc.date.submitted2016-11-14
dc.identifier.citationWorm. 2015 Jul 9;4(3):e1062971. doi: 10.1080/21624054.2015.1062971. <a href="http://dx.doi.org/10.1080/21624054.2015.1062971">Link to article on publisher's site</a>
dc.identifier.issn2162-4046 (Linking)
dc.identifier.doi10.1080/21624054.2015.1062971
dc.identifier.pmid26430569
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37921
dc.description.abstractNeuromodulation enables transient restructuring of anatomically fixed neural circuits, generating alternate outputs and distinct states that allow for flexible organismal responses to changing conditions. We recently identified a requirement for the neuropeptide-like protein NLP-12, a Caenorhabditis elegans homolog of mammalian Cholecystokinin (CCK), in the control of behavioral responses to altered food availability. We showed that deletion of nlp-12 impairs turning during local food searching while nlp-12 overexpression is sufficient to induce deep body bends and enhance turning. nlp-12 is solely expressed in the DVA interneuron that is located postsynaptic to the dopaminergic PDE neurons and presynaptic to premotor and motor neurons, well-positioned for modulating sensorimotor tasks. Interestingly, DVA was previously implicated in a NLP-12 mediated proprioceptive feedback loop during C. elegans locomotion. Here, we discuss the modulatory effects of NLP-12 with an emphasis on the potential for circuit level integration with olfactory information about food availability. In addition, we propose potential mechanisms by which DVA may integrate distinct forms of sensory information to regulate NLP-12 signaling and mediate context-dependent modulation of the motor circuit.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26430569&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588156/
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/
dc.subjectforaging
dc.subjectmotor control
dc.subjectneuromodulation
dc.subjectneuropeptide
dc.subjectsynapse
dc.subjectBehavioral Neurobiology
dc.titleIn the proper context: Neuropeptide regulation of behavioral transitions during food searching
dc.typeJournal Article
dc.source.journaltitleWorm
dc.source.volume4
dc.source.issue3
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1194&amp;context=neurobiology_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neurobiology_pp/195
dc.identifier.contextkey9373682
refterms.dateFOA2022-08-23T16:32:37Z
html.description.abstract<p>Neuromodulation enables transient restructuring of anatomically fixed neural circuits, generating alternate outputs and distinct states that allow for flexible organismal responses to changing conditions. We recently identified a requirement for the neuropeptide-like protein NLP-12, a Caenorhabditis elegans homolog of mammalian Cholecystokinin (CCK), in the control of behavioral responses to altered food availability. We showed that deletion of nlp-12 impairs turning during local food searching while nlp-12 overexpression is sufficient to induce deep body bends and enhance turning. nlp-12 is solely expressed in the DVA interneuron that is located postsynaptic to the dopaminergic PDE neurons and presynaptic to premotor and motor neurons, well-positioned for modulating sensorimotor tasks. Interestingly, DVA was previously implicated in a NLP-12 mediated proprioceptive feedback loop during C. elegans locomotion. Here, we discuss the modulatory effects of NLP-12 with an emphasis on the potential for circuit level integration with olfactory information about food availability. In addition, we propose potential mechanisms by which DVA may integrate distinct forms of sensory information to regulate NLP-12 signaling and mediate context-dependent modulation of the motor circuit.</p>
dc.identifier.submissionpathneurobiology_pp/195
dc.contributor.departmentFrancis Lab
dc.contributor.departmentNeurobiology
dc.source.pagese1062971


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