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Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution
Rhabdomeric opsins (r-opsins) are light sensors in cephalic eye photoreceptors, but also function in additional sensory organs. This has prompted questions on the evolutionary relationship of these cell types, and if ancient r-opsins were non-photosensory. A molecular profiling approach in the marin...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367381/ https://www.ncbi.nlm.nih.gov/pubmed/34350831 http://dx.doi.org/10.7554/eLife.66144 |
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author | Revilla-i-Domingo, Roger Rajan, Vinoth Babu Veedin Waldherr, Monika Prohaczka, Günther Musset, Hugo Orel, Lukas Gerrard, Elliot Smolka, Moritz Stockinger, Alexander Farlik, Matthias Lucas, Robert J Raible, Florian Tessmar-Raible, Kristin |
author_facet | Revilla-i-Domingo, Roger Rajan, Vinoth Babu Veedin Waldherr, Monika Prohaczka, Günther Musset, Hugo Orel, Lukas Gerrard, Elliot Smolka, Moritz Stockinger, Alexander Farlik, Matthias Lucas, Robert J Raible, Florian Tessmar-Raible, Kristin |
author_sort | Revilla-i-Domingo, Roger |
collection | PubMed |
description | Rhabdomeric opsins (r-opsins) are light sensors in cephalic eye photoreceptors, but also function in additional sensory organs. This has prompted questions on the evolutionary relationship of these cell types, and if ancient r-opsins were non-photosensory. A molecular profiling approach in the marine bristleworm Platynereis dumerilii revealed shared and distinct features of cephalic and non-cephalic r-opsin1-expressing cells. Non-cephalic cells possess a full set of phototransduction components, but also a mechanosensory signature. Prompted by the latter, we investigated Platynereis putative mechanotransducer and found that nompc and pkd2.1 co-expressed with r-opsin1 in TRE cells by HCR RNA-FISH. To further assess the role of r-Opsin1 in these cells, we studied its signaling properties and unraveled that r-Opsin1 is a Gαq-coupled blue light receptor. Profiling of cells from r-opsin1 mutants versus wild-types, and a comparison under different light conditions reveals that in the non-cephalic cells light – mediated by r-Opsin1 – adjusts the expression level of a calcium transporter relevant for auditory mechanosensation in vertebrates. We establish a deep-learning-based quantitative behavioral analysis for animal trunk movements and identify a light– and r-Opsin-1–dependent fine-tuning of the worm's undulatory movements in headless trunks, which are known to require mechanosensory feedback. Our results provide new data on peripheral cell types of likely light sensory/mechanosensory nature. These results point towards a concept in which such a multisensory cell type evolved to allow for fine-tuning of mechanosensation by light. This implies that light-independent mechanosensory roles of r-opsins may have evolved secondarily. |
format | Online Article Text |
id | pubmed-8367381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-83673812021-08-18 Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution Revilla-i-Domingo, Roger Rajan, Vinoth Babu Veedin Waldherr, Monika Prohaczka, Günther Musset, Hugo Orel, Lukas Gerrard, Elliot Smolka, Moritz Stockinger, Alexander Farlik, Matthias Lucas, Robert J Raible, Florian Tessmar-Raible, Kristin eLife Developmental Biology Rhabdomeric opsins (r-opsins) are light sensors in cephalic eye photoreceptors, but also function in additional sensory organs. This has prompted questions on the evolutionary relationship of these cell types, and if ancient r-opsins were non-photosensory. A molecular profiling approach in the marine bristleworm Platynereis dumerilii revealed shared and distinct features of cephalic and non-cephalic r-opsin1-expressing cells. Non-cephalic cells possess a full set of phototransduction components, but also a mechanosensory signature. Prompted by the latter, we investigated Platynereis putative mechanotransducer and found that nompc and pkd2.1 co-expressed with r-opsin1 in TRE cells by HCR RNA-FISH. To further assess the role of r-Opsin1 in these cells, we studied its signaling properties and unraveled that r-Opsin1 is a Gαq-coupled blue light receptor. Profiling of cells from r-opsin1 mutants versus wild-types, and a comparison under different light conditions reveals that in the non-cephalic cells light – mediated by r-Opsin1 – adjusts the expression level of a calcium transporter relevant for auditory mechanosensation in vertebrates. We establish a deep-learning-based quantitative behavioral analysis for animal trunk movements and identify a light– and r-Opsin-1–dependent fine-tuning of the worm's undulatory movements in headless trunks, which are known to require mechanosensory feedback. Our results provide new data on peripheral cell types of likely light sensory/mechanosensory nature. These results point towards a concept in which such a multisensory cell type evolved to allow for fine-tuning of mechanosensation by light. This implies that light-independent mechanosensory roles of r-opsins may have evolved secondarily. eLife Sciences Publications, Ltd 2021-08-05 /pmc/articles/PMC8367381/ /pubmed/34350831 http://dx.doi.org/10.7554/eLife.66144 Text en © 2021, Revilla-i-Domingo et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Revilla-i-Domingo, Roger Rajan, Vinoth Babu Veedin Waldherr, Monika Prohaczka, Günther Musset, Hugo Orel, Lukas Gerrard, Elliot Smolka, Moritz Stockinger, Alexander Farlik, Matthias Lucas, Robert J Raible, Florian Tessmar-Raible, Kristin Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title | Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title_full | Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title_fullStr | Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title_full_unstemmed | Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title_short | Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
title_sort | characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo- and mechanoreceptor evolution |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367381/ https://www.ncbi.nlm.nih.gov/pubmed/34350831 http://dx.doi.org/10.7554/eLife.66144 |
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