Zebrafish use spectral information to suppress the visual background

Vision first evolved in the water, where the spectral content of light informs about viewing distance. However, whether and how aquatic visual systems exploit this "fact of physics" remains unknown. Here, we show that zebrafish use "color" information to suppress responses to the visual background. For this, zebrafish divide their intact ancestral cone complement into two opposing systems: PR1/4 ("red/UV cones") versus PR2/3 ("green/blue cones"). Of these, the achromatic PR1 and PR4, which are retained in mammals, are necessary and sufficient for vision. By contrast, the color-opponent PR2 and PR3, which are lost in mammals, are neither necessary nor sufficient for vision. Instead, they form an "auxiliary" system that spectrally suppresses the "core" drive from PR1 and PR4. Our insights challenge the long-held notion that vertebrate cone diversity primarily serves color vision and further hint at terrestrialization, not nocturnalization, as the leading driver for visual circuit reorganization in mammals.

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Publication Details

Journal
Cell
Published
2025-11-03
DOI
https://doi.org/10.1016/j.cell.2025.10.009
Citations
1
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.81
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article

Zebrafish use spectral information to suppress the visual background

Thomas Euler, Tom Baden, Chiara Fornetto
1 citations
Cell
Retinal Development and Disorders
0.81
article

Zebrafish use spectral information to suppress the visual background

Thomas Euler, Tom Baden, Chiara Fornetto
article en
1 citations

Abstract

Vision first evolved in the water, where the spectral content of light informs about viewing distance. However, whether and how aquatic visual systems exploit this "fact of physics" remains unknown. Here, we show that zebrafish use "color" information to suppress responses to the visual background. For this, zebrafish divide their intact ancestral cone complement into two opposing systems: PR1/4 ("red/UV cones") versus PR2/3 ("green/blue cones"). Of these, the achromatic PR1 and PR4, which are retained in mammals, are necessary and sufficient for vision. By contrast, the color-opponent PR2 and PR3, which are lost in mammals, are neither necessary nor sufficient for vision. Instead, they form an "auxiliary" system that spectrally suppresses the "core" drive from PR1 and PR4. Our insights challenge the long-held notion that vertebrate cone diversity primarily serves color vision and further hint at terrestrialization, not nocturnalization, as the leading driver for visual circuit reorganization in mammals.

CellVol. 188(26)
University of Sussex (GB), Bernstein Center for Computational Neuroscience Tübingen (DE)
Openalex Percentile: Top 22%
Retinal Development and Disorders
0.81
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