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Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity
During development, the nervous system generates neurons that serve highly specialized roles and, accordingly, possess unique functional attributes. The chemosensory BAG neurons of C. elegans are striking exemplars of this. BAGs sense the respiratory gas carbon dioxide (CO(2)) and, in a context-depe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706712/ https://www.ncbi.nlm.nih.gov/pubmed/33184226 http://dx.doi.org/10.1101/gad.342212.120 |
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author | Rossillo, Mary Ringstad, Niels |
author_facet | Rossillo, Mary Ringstad, Niels |
author_sort | Rossillo, Mary |
collection | PubMed |
description | During development, the nervous system generates neurons that serve highly specialized roles and, accordingly, possess unique functional attributes. The chemosensory BAG neurons of C. elegans are striking exemplars of this. BAGs sense the respiratory gas carbon dioxide (CO(2)) and, in a context-dependent manner, switch from mediating avoidance of CO(2) to supporting CO(2) attraction. To determine mechanisms that support the physiology and plasticity of BAG neurons, we used tandem ChIP-seq and cell targeted RNA-seq to identify gene targets of the transcription factor ETS-5, which is required for BAG development. A functional screen of ETS-5 targets revealed that NHR-6, the sole C. elegans NR4A-type nuclear receptor, is required for BAG-mediated avoidance of CO(2) and regulates expression of a subset of BAG-specific genes. Unlike ets-5 mutants, which are defective for both attraction to and avoidance of CO(2), nhr-6 mutants are fully competent for attraction. These data indicate that the remarkable ability of BAGs to adaptively assign positive or negative valence to a chemosensory stimulus requires a gene-regulatory program supported by an evolutionarily conserved type of nuclear receptor. We suggest that NHR-6 might be an example of a developmental mechanism for modular encoding of functional plasticity in the nervous system. |
format | Online Article Text |
id | pubmed-7706712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77067122021-06-01 Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity Rossillo, Mary Ringstad, Niels Genes Dev Research Paper During development, the nervous system generates neurons that serve highly specialized roles and, accordingly, possess unique functional attributes. The chemosensory BAG neurons of C. elegans are striking exemplars of this. BAGs sense the respiratory gas carbon dioxide (CO(2)) and, in a context-dependent manner, switch from mediating avoidance of CO(2) to supporting CO(2) attraction. To determine mechanisms that support the physiology and plasticity of BAG neurons, we used tandem ChIP-seq and cell targeted RNA-seq to identify gene targets of the transcription factor ETS-5, which is required for BAG development. A functional screen of ETS-5 targets revealed that NHR-6, the sole C. elegans NR4A-type nuclear receptor, is required for BAG-mediated avoidance of CO(2) and regulates expression of a subset of BAG-specific genes. Unlike ets-5 mutants, which are defective for both attraction to and avoidance of CO(2), nhr-6 mutants are fully competent for attraction. These data indicate that the remarkable ability of BAGs to adaptively assign positive or negative valence to a chemosensory stimulus requires a gene-regulatory program supported by an evolutionarily conserved type of nuclear receptor. We suggest that NHR-6 might be an example of a developmental mechanism for modular encoding of functional plasticity in the nervous system. Cold Spring Harbor Laboratory Press 2020-12-01 /pmc/articles/PMC7706712/ /pubmed/33184226 http://dx.doi.org/10.1101/gad.342212.120 Text en © 2020 Rossillo and Ringstad; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Rossillo, Mary Ringstad, Niels Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title | Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title_full | Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title_fullStr | Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title_full_unstemmed | Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title_short | Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
title_sort | development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706712/ https://www.ncbi.nlm.nih.gov/pubmed/33184226 http://dx.doi.org/10.1101/gad.342212.120 |
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