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A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling

Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching betw...

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Autores principales: Nagy, Stanislav, Wright, Charles, Tramm, Nora, Labello, Nicholas, Burov, Stanislav, Biron, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699835/
https://www.ncbi.nlm.nih.gov/pubmed/23840929
http://dx.doi.org/10.7554/eLife.00782
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author Nagy, Stanislav
Wright, Charles
Tramm, Nora
Labello, Nicholas
Burov, Stanislav
Biron, David
author_facet Nagy, Stanislav
Wright, Charles
Tramm, Nora
Labello, Nicholas
Burov, Stanislav
Biron, David
author_sort Nagy, Stanislav
collection PubMed
description Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching between two distinct behavioral states: active wakefulness and quiet wakefulness. The durations of epochs of active wakefulness exhibited non-Poisson statistics. Increased G(αs) signaling stabilized the active wakefulness state before, during and after lethargus. In contrast, decreased G(αs) signaling, decreased neuropeptide release, or decreased CREB activity destabilized active wakefulness outside of, but not during, lethargus. Taken together, our findings support a model in which protein kinase A (PKA) stabilizes active wakefulness, at least in part through two of its downstream targets: neuropeptide release and CREB. However, during lethargus, when active wakefulness is strongly suppressed, the native role of PKA signaling in modulating locomotion and quiescence may be minor. DOI: http://dx.doi.org/10.7554/eLife.00782.001
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spelling pubmed-36998352013-07-09 A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling Nagy, Stanislav Wright, Charles Tramm, Nora Labello, Nicholas Burov, Stanislav Biron, David eLife Neuroscience Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching between two distinct behavioral states: active wakefulness and quiet wakefulness. The durations of epochs of active wakefulness exhibited non-Poisson statistics. Increased G(αs) signaling stabilized the active wakefulness state before, during and after lethargus. In contrast, decreased G(αs) signaling, decreased neuropeptide release, or decreased CREB activity destabilized active wakefulness outside of, but not during, lethargus. Taken together, our findings support a model in which protein kinase A (PKA) stabilizes active wakefulness, at least in part through two of its downstream targets: neuropeptide release and CREB. However, during lethargus, when active wakefulness is strongly suppressed, the native role of PKA signaling in modulating locomotion and quiescence may be minor. DOI: http://dx.doi.org/10.7554/eLife.00782.001 eLife Sciences Publications, Ltd 2013-07-02 /pmc/articles/PMC3699835/ /pubmed/23840929 http://dx.doi.org/10.7554/eLife.00782 Text en Copyright © 2013, Nagy et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Nagy, Stanislav
Wright, Charles
Tramm, Nora
Labello, Nicholas
Burov, Stanislav
Biron, David
A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title_full A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title_fullStr A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title_full_unstemmed A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title_short A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by G(αs) signaling
title_sort longitudinal study of caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by g(αs) signaling
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699835/
https://www.ncbi.nlm.nih.gov/pubmed/23840929
http://dx.doi.org/10.7554/eLife.00782
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