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  4. C. elegans Notch Signaling Regulates Adult Chemosensory Response and Larval Molting Quiescence

C. elegans Notch Signaling Regulates Adult Chemosensory Response and Larval Molting Quiescence

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Author(s)
Singh, Komudi
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Chao, Michael Y.
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Somers, Gerard A.
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Komatsu, Hidetoshi
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Corkins, Mark E.
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Larkins-Ford, Jonah
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Tucey, Tim
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Dionne, Heather M.
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Walsh, Melissa B.
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Beaumont, Emma K.
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Date Issued
May 2011
Journal
Current Biology
Publisher
Elsevier B.V.
Citation
Singh, Komudi, Michael Y. Chao, Gerard A. Somers, Hidetoshi Komatsu, Mark E. Corkins, Jonah Larkins-Ford, Tim Tucey, et al. “C. Elegans Notch Signaling Regulates Adult Chemosensory Response and Larval Molting Quiescence.” Current Biology 21, no. 10 (May 2011): 825–834. © 2011 Elsevier Ltd.
Version
Final published version
Abstract
Background: The conserved DOS-motif proteins OSM-7 and OSM-11 function as coligands with canonical DSL (Delta, Serrate, and LAG-2) ligands to activate C. elegans Notch receptors during development. We report here that Notch ligands, coligands, and the receptors LIN-12 and GLP-1 regulate two C. elegans behaviors: chemosensory avoidance of octanol and quiescence during molting lethargus. Results: C. elegans lacking osm-7 or osm-11 are defective in their response to octanol. We find that OSM-11 is secreted from hypodermal seam cells into the pseudocoelomic body cavity and acts non-cell autonomously as a diffusible factor. OSM-11 acts with the DSL ligand LAG-2 to activate LIN-12 and GLP-1 Notch receptors in the neurons of adult animals, thereby regulating octanol avoidance response. In adult animals, overexpression of osm-11 and consequent Notch receptor activation induces anachronistic sleep-like quiescence. Perturbation of Notch signaling alters basal activity in adults as well as arousal thresholds and quiescence during molting lethargus. Genetic epistasis studies reveal that Notch signaling regulates quiescence via previously identified circuits and genetic pathways including the egl-4 cGMP-dependent kinase. Conclusions: Our findings indicate that the conserved Notch pathway modulates behavior in adult C. elegans in response to environmental stress. Additionally, Notch signaling regulates sleep-like quiescence in C. elegans, suggesting that Notch may regulate sleep in other species.
MIT Department
Massachusetts Institute of Technology. Department of Mechanical Engineering
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/92490
DOI of Published Version
https://doi.org/10.1016/j.cub.2011.04.010
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