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The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition

Behavioral plasticity is widespread in swarming animals, but little is known about its underlying neural and molecular mechanisms. Here, we report that a neuropeptide F (NPF)/nitric oxide (NO) pathway plays a critical role in the locomotor plasticity of swarming migratory locusts. The transcripts en...

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Autores principales: Hou, Li, Yang, Pengcheng, Jiang, Feng, Liu, Qing, Wang, Xianhui, Kang, Le
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400507/
https://www.ncbi.nlm.nih.gov/pubmed/28346142
http://dx.doi.org/10.7554/eLife.22526
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author Hou, Li
Yang, Pengcheng
Jiang, Feng
Liu, Qing
Wang, Xianhui
Kang, Le
author_facet Hou, Li
Yang, Pengcheng
Jiang, Feng
Liu, Qing
Wang, Xianhui
Kang, Le
author_sort Hou, Li
collection PubMed
description Behavioral plasticity is widespread in swarming animals, but little is known about its underlying neural and molecular mechanisms. Here, we report that a neuropeptide F (NPF)/nitric oxide (NO) pathway plays a critical role in the locomotor plasticity of swarming migratory locusts. The transcripts encoding two related neuropeptides, NPF1a and NPF2, show reduced levels during crowding, and the transcript levels of NPF1a and NPF2 receptors significantly increase during locust isolation. Both NPF1a and NPF2 have suppressive effects on phase-related locomotor activity. A key downstream mediator for both NPFs is nitric oxide synthase (NOS), which regulates phase-related locomotor activity by controlling NO synthesis in the locust brain. Mechanistically, NPF1a and NPF2 modify NOS activity by separately suppressing its phosphorylation and by lowering its transcript level, effects that are mediated by their respective receptors. Our results uncover a hierarchical neurochemical mechanism underlying behavioral plasticity in the swarming locust and provide insights into the NPF/NO axis. DOI: http://dx.doi.org/10.7554/eLife.22526.001
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spelling pubmed-54005072017-04-24 The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition Hou, Li Yang, Pengcheng Jiang, Feng Liu, Qing Wang, Xianhui Kang, Le eLife Biochemistry Behavioral plasticity is widespread in swarming animals, but little is known about its underlying neural and molecular mechanisms. Here, we report that a neuropeptide F (NPF)/nitric oxide (NO) pathway plays a critical role in the locomotor plasticity of swarming migratory locusts. The transcripts encoding two related neuropeptides, NPF1a and NPF2, show reduced levels during crowding, and the transcript levels of NPF1a and NPF2 receptors significantly increase during locust isolation. Both NPF1a and NPF2 have suppressive effects on phase-related locomotor activity. A key downstream mediator for both NPFs is nitric oxide synthase (NOS), which regulates phase-related locomotor activity by controlling NO synthesis in the locust brain. Mechanistically, NPF1a and NPF2 modify NOS activity by separately suppressing its phosphorylation and by lowering its transcript level, effects that are mediated by their respective receptors. Our results uncover a hierarchical neurochemical mechanism underlying behavioral plasticity in the swarming locust and provide insights into the NPF/NO axis. DOI: http://dx.doi.org/10.7554/eLife.22526.001 eLife Sciences Publications, Ltd 2017-03-27 /pmc/articles/PMC5400507/ /pubmed/28346142 http://dx.doi.org/10.7554/eLife.22526 Text en © 2017, Hou et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry
Hou, Li
Yang, Pengcheng
Jiang, Feng
Liu, Qing
Wang, Xianhui
Kang, Le
The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title_full The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title_fullStr The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title_full_unstemmed The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title_short The neuropeptide F/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
title_sort neuropeptide f/nitric oxide pathway is essential for shaping locomotor plasticity underlying locust phase transition
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400507/
https://www.ncbi.nlm.nih.gov/pubmed/28346142
http://dx.doi.org/10.7554/eLife.22526
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