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Ancestral circuits for vertebrate color vision emerge at the first retinal synapse

For color vision, retinal circuits separate information about intensity and wavelength. In vertebrates that use the full complement of four “ancestral” cone types, the nature and implementation of this computation remain poorly understood. Here, we establish the complete circuit architecture of oute...

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Autores principales: Yoshimatsu, Takeshi, Bartel, Philipp, Schröder, Cornelius, Janiak, Filip K., St-Pierre, François, Berens, Philipp, Baden, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514090/
https://www.ncbi.nlm.nih.gov/pubmed/34644120
http://dx.doi.org/10.1126/sciadv.abj6815
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author Yoshimatsu, Takeshi
Bartel, Philipp
Schröder, Cornelius
Janiak, Filip K.
St-Pierre, François
Berens, Philipp
Baden, Tom
author_facet Yoshimatsu, Takeshi
Bartel, Philipp
Schröder, Cornelius
Janiak, Filip K.
St-Pierre, François
Berens, Philipp
Baden, Tom
author_sort Yoshimatsu, Takeshi
collection PubMed
description For color vision, retinal circuits separate information about intensity and wavelength. In vertebrates that use the full complement of four “ancestral” cone types, the nature and implementation of this computation remain poorly understood. Here, we establish the complete circuit architecture of outer retinal circuits underlying color processing in larval zebrafish. We find that the synaptic outputs of red and green cones efficiently rotate the encoding of natural daylight in a principal components analysis–like manner to yield primary achromatic and spectrally opponent axes, respectively. Blue cones are tuned to capture most remaining variance when opposed to green cones, while UV cone present a UV achromatic axis for prey capture. We note that fruitflies use essentially the same strategy. Therefore, rotating color space into primary achromatic and chromatic axes at the eye’s first synapse may thus be a fundamental principle of color vision when using more than two spectrally well-separated photoreceptor types.
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spelling pubmed-85140902021-10-22 Ancestral circuits for vertebrate color vision emerge at the first retinal synapse Yoshimatsu, Takeshi Bartel, Philipp Schröder, Cornelius Janiak, Filip K. St-Pierre, François Berens, Philipp Baden, Tom Sci Adv Neuroscience For color vision, retinal circuits separate information about intensity and wavelength. In vertebrates that use the full complement of four “ancestral” cone types, the nature and implementation of this computation remain poorly understood. Here, we establish the complete circuit architecture of outer retinal circuits underlying color processing in larval zebrafish. We find that the synaptic outputs of red and green cones efficiently rotate the encoding of natural daylight in a principal components analysis–like manner to yield primary achromatic and spectrally opponent axes, respectively. Blue cones are tuned to capture most remaining variance when opposed to green cones, while UV cone present a UV achromatic axis for prey capture. We note that fruitflies use essentially the same strategy. Therefore, rotating color space into primary achromatic and chromatic axes at the eye’s first synapse may thus be a fundamental principle of color vision when using more than two spectrally well-separated photoreceptor types. American Association for the Advancement of Science 2021-10-13 /pmc/articles/PMC8514090/ /pubmed/34644120 http://dx.doi.org/10.1126/sciadv.abj6815 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Yoshimatsu, Takeshi
Bartel, Philipp
Schröder, Cornelius
Janiak, Filip K.
St-Pierre, François
Berens, Philipp
Baden, Tom
Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title_full Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title_fullStr Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title_full_unstemmed Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title_short Ancestral circuits for vertebrate color vision emerge at the first retinal synapse
title_sort ancestral circuits for vertebrate color vision emerge at the first retinal synapse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514090/
https://www.ncbi.nlm.nih.gov/pubmed/34644120
http://dx.doi.org/10.1126/sciadv.abj6815
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