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Network control principles predict neuron function in the Caenorhabditis elegans connectome
Recent studies on the controllability of complex systems offer a powerful mathematical framework to systematically explore the structure-function relationship in biological, social and technological networks1–3. Despite theoretical advances, we lack direct experimental proof of the validity of these...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710776/ https://www.ncbi.nlm.nih.gov/pubmed/29045391 http://dx.doi.org/10.1038/nature24056 |
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author | Yan, Gang Vértes, Petra E. Towlson, Emma K. Chew, Yee Lian Walker, Denise S. Schafer, William R. Barabási, Albert-László |
author_facet | Yan, Gang Vértes, Petra E. Towlson, Emma K. Chew, Yee Lian Walker, Denise S. Schafer, William R. Barabási, Albert-László |
author_sort | Yan, Gang |
collection | PubMed |
description | Recent studies on the controllability of complex systems offer a powerful mathematical framework to systematically explore the structure-function relationship in biological, social and technological networks1–3. Despite theoretical advances, we lack direct experimental proof of the validity of these widely used control principles. Here we fill this gap by applying a control framework to the connectome of the nematode C. elegans4–6, allowing us to predict the involvement of each C. elegans neuron in locomotor behaviours. We predict that control of the muscles or motor neurons requires twelve neuronal classes, which include neuronal groups previously implicated in locomotion by laser ablation7–13, as well as one previously uncharacterised neuron, PDB. We validate this prediction experimentally, finding that the ablation of PDB leads to a significant loss of dorsoventral polarity in large body bends. Importantly, control principles also allow us to investigate the involvement of individual neurons within each neuronal class. For example, we predict that, within the class of DD motor neurons, only three (DD04, DD05, or DD06) should affect locomotion when ablated individually. This prediction is also confirmed, with single-cell ablations of DD04 or DD05, but not DD02 or DD03, specifically affecting posterior body movements. Our predictions are robust to deletions of weak connections, missing connections, and rewired connections in the current connectome, indicating the potential applicability of this analytical framework to larger and less well-characterised connectomes. |
format | Online Article Text |
id | pubmed-5710776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-57107762018-04-18 Network control principles predict neuron function in the Caenorhabditis elegans connectome Yan, Gang Vértes, Petra E. Towlson, Emma K. Chew, Yee Lian Walker, Denise S. Schafer, William R. Barabási, Albert-László Nature Article Recent studies on the controllability of complex systems offer a powerful mathematical framework to systematically explore the structure-function relationship in biological, social and technological networks1–3. Despite theoretical advances, we lack direct experimental proof of the validity of these widely used control principles. Here we fill this gap by applying a control framework to the connectome of the nematode C. elegans4–6, allowing us to predict the involvement of each C. elegans neuron in locomotor behaviours. We predict that control of the muscles or motor neurons requires twelve neuronal classes, which include neuronal groups previously implicated in locomotion by laser ablation7–13, as well as one previously uncharacterised neuron, PDB. We validate this prediction experimentally, finding that the ablation of PDB leads to a significant loss of dorsoventral polarity in large body bends. Importantly, control principles also allow us to investigate the involvement of individual neurons within each neuronal class. For example, we predict that, within the class of DD motor neurons, only three (DD04, DD05, or DD06) should affect locomotion when ablated individually. This prediction is also confirmed, with single-cell ablations of DD04 or DD05, but not DD02 or DD03, specifically affecting posterior body movements. Our predictions are robust to deletions of weak connections, missing connections, and rewired connections in the current connectome, indicating the potential applicability of this analytical framework to larger and less well-characterised connectomes. 2017-10-18 2017-10-26 /pmc/articles/PMC5710776/ /pubmed/29045391 http://dx.doi.org/10.1038/nature24056 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Yan, Gang Vértes, Petra E. Towlson, Emma K. Chew, Yee Lian Walker, Denise S. Schafer, William R. Barabási, Albert-László Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title | Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title_full | Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title_fullStr | Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title_full_unstemmed | Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title_short | Network control principles predict neuron function in the Caenorhabditis elegans connectome |
title_sort | network control principles predict neuron function in the caenorhabditis elegans connectome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710776/ https://www.ncbi.nlm.nih.gov/pubmed/29045391 http://dx.doi.org/10.1038/nature24056 |
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