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Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion

Using a computational model of the Caenorhabditis elegans connectome dynamics, we show that proprioceptive feedback is necessary for sustained dynamic responses to external input. This is consistent with the lack of biophysical evidence for a central pattern generator, and recent experimental eviden...

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Detalles Bibliográficos
Autores principales: Kunert, James M., Proctor, Joshua L., Brunton, Steven L., Kutz, J. Nathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226684/
https://www.ncbi.nlm.nih.gov/pubmed/28076347
http://dx.doi.org/10.1371/journal.pcbi.1005303
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author Kunert, James M.
Proctor, Joshua L.
Brunton, Steven L.
Kutz, J. Nathan
author_facet Kunert, James M.
Proctor, Joshua L.
Brunton, Steven L.
Kutz, J. Nathan
author_sort Kunert, James M.
collection PubMed
description Using a computational model of the Caenorhabditis elegans connectome dynamics, we show that proprioceptive feedback is necessary for sustained dynamic responses to external input. This is consistent with the lack of biophysical evidence for a central pattern generator, and recent experimental evidence that proprioception drives locomotion. The low-dimensional functional response of the Caenorhabditis elegans network of neurons to proprioception-like feedback is optimized by input of specific spatial wavelengths which correspond to the spatial scale of real body shape dynamics. Furthermore, we find that the motor subcircuit of the network is responsible for regulating this response, in agreement with experimental expectations. To explore how the connectomic dynamics produces the observed two-mode, oscillatory limit cycle behavior from a static fixed point, we probe the fixed point’s low-dimensional structure using Dynamic Mode Decomposition. This reveals that the nonlinear network dynamics encode six clusters of dynamic modes, with timescales spanning three orders of magnitude. Two of these six dynamic mode clusters correspond to previously-discovered behavioral modes related to locomotion. These dynamic modes and their timescales are encoded by the network’s degree distribution and specific connectivity. This suggests that behavioral dynamics are partially encoded within the connectome itself, the connectivity of which facilitates proprioceptive control.
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spelling pubmed-52266842017-01-31 Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion Kunert, James M. Proctor, Joshua L. Brunton, Steven L. Kutz, J. Nathan PLoS Comput Biol Research Article Using a computational model of the Caenorhabditis elegans connectome dynamics, we show that proprioceptive feedback is necessary for sustained dynamic responses to external input. This is consistent with the lack of biophysical evidence for a central pattern generator, and recent experimental evidence that proprioception drives locomotion. The low-dimensional functional response of the Caenorhabditis elegans network of neurons to proprioception-like feedback is optimized by input of specific spatial wavelengths which correspond to the spatial scale of real body shape dynamics. Furthermore, we find that the motor subcircuit of the network is responsible for regulating this response, in agreement with experimental expectations. To explore how the connectomic dynamics produces the observed two-mode, oscillatory limit cycle behavior from a static fixed point, we probe the fixed point’s low-dimensional structure using Dynamic Mode Decomposition. This reveals that the nonlinear network dynamics encode six clusters of dynamic modes, with timescales spanning three orders of magnitude. Two of these six dynamic mode clusters correspond to previously-discovered behavioral modes related to locomotion. These dynamic modes and their timescales are encoded by the network’s degree distribution and specific connectivity. This suggests that behavioral dynamics are partially encoded within the connectome itself, the connectivity of which facilitates proprioceptive control. Public Library of Science 2017-01-11 /pmc/articles/PMC5226684/ /pubmed/28076347 http://dx.doi.org/10.1371/journal.pcbi.1005303 Text en © 2017 Kunert et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kunert, James M.
Proctor, Joshua L.
Brunton, Steven L.
Kutz, J. Nathan
Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title_full Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title_fullStr Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title_full_unstemmed Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title_short Spatiotemporal Feedback and Network Structure Drive and Encode Caenorhabditis elegans Locomotion
title_sort spatiotemporal feedback and network structure drive and encode caenorhabditis elegans locomotion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226684/
https://www.ncbi.nlm.nih.gov/pubmed/28076347
http://dx.doi.org/10.1371/journal.pcbi.1005303
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