TY - JOUR
T1 - Characterization of cephalic and non-cephalic sensory cell types provides insight into joint photo-and mechanoreceptor evolution
AU - Revilla-I-domingo, Roger
AU - Rajan, Vinoth Babu Veedin
AU - Waldherr, Monika
AU - Prohaczka, Günther
AU - Musset, Hugo
AU - Orel, Lukas
AU - Gerrard, Elliot
AU - Smolka, Moritz
AU - Stockinger, Alexander
AU - Farlik, Matthias
AU - Lucas, Robert J.
AU - Raible, Florian
AU - Tessmar-Raible, Kristin
N1 - Funding Information:
The research leading to these results has received funding from the European Research Council under the European Community‘s Seventh Framework Programme (FP7/2007–2013)/ERC Grant Agreement 260304 (FR) and ERC Grant Agreement 337011 (KT-R); the research platforms ‘Rhythms of Life’ (KT-R, FR, AvH) and ‘Single-cell genomics of stem cells’ (FR) of the University of Vienna; the Austrian Science Fund (FWF) START award, project Y413 (KT-R); Austrian Science Fund (FWF) projects P28970 (KT-R), P30035, I2972 (FR), and SFB F78 (FR and KT-R). AvH and MS acknowledge financial support from the University of Vienna and the Medical University of Vienna. RR was supported by the Vienna International PostDoctoral Program for Molecular Life Sciences (VIPS). None of the funding bodies was involved in the design of the study, the collection, analysis, and interpretation of data or in writing the manuscript.
Funding Information:
We thank the members of the Tessmar-Raible and Raible groups for discussions, Aida ?ori? and Dunja Rokvic for experimental help, Christoph Bock for support with RNA amplification, and Andrij Belokurov, Margaryta Borysova, and Netsanet Getachew for help with worm care and genotyping at the Max Perutz Labs aquatic facility. The research leading to these results has received funding from the European Research Council under the European Community?s Seventh Framework Programme (FP7/2007?2013)/ERC Grant Agreement 260304 (FR) and ERC Grant Agreement 337011 (KT-R); the research platforms ?Rhythms of Life? (KT-R, FR, AvH) and ?Single-cell genomics of stem cells? (FR) of the University of Vienna; the Austrian Science Fund (FWF) START award, project Y413 (KT-R); Austrian Science Fund (FWF) projects P28970 (KT-R), P30035, I2972 (FR), and SFB F78 (FR and KT-R). AvH and MS acknowledge financial support from the University of Vienna and the Medical University of Vienna. RR was supported by the Vienna International PostDoctoral Program for Molecular Life Sciences (VIPS). None of the funding bodies was involved in the design of the study, the collection, analysis, and interpretation of data or in writing the manuscript.
Publisher Copyright:
© Revilla-i-Domingo et al.
PY - 2021/8/5
Y1 - 2021/8/5
N2 - 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 Gaq-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.
AB - 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 Gaq-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.
UR - http://www.scopus.com/inward/record.url?scp=85113767490&partnerID=8YFLogxK
U2 - 10.7554/ELIFE.66144
DO - 10.7554/ELIFE.66144
M3 - Article
C2 - 34350831
AN - SCOPUS:85113767490
SN - 2050-084X
VL - 10
JO - eLife
JF - eLife
M1 - e66144
ER -