4.5 Article

Avian Binocularity and Adaptation to Nocturnal Environments: Genomic Insights from a Highly Derived Visual Phenotype

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 11, Issue 8, Pages 2244-2255

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evz111

Keywords

relaxed and intensified evolution; pseudogenization; eye-development; coevolution; barn owl; ocular adaptations

Funding

  1. Fundacao para a Ciencia e a Tecnologia (FCT) [SFRH/BD/79850/2011, SFRH/BD/71041/2010]
  2. National Research Council Research Associateship Award at the Walter Reed Army Institute of Research
  3. Russian Science Foundation [17-14-01138]
  4. St. Petersburg State University [1.52.1647.2016]
  5. Howard Hughes Medical Institute
  6. FCT [UID/Multi/04423/2019]
  7. European Regional Development Fund (ERDF)
  8. European Structural and Investment Funds (ESIF) through the Competitiveness and Internationalization Operational Program-COMPETE 2020
  9. National Funds through the FCT [PTDC/AAG-GLO/6887/2014 (POCI-01-0124-FEDER-016845)]
  10. Fundação para a Ciência e a Tecnologia [SFRH/BD/79850/2011, SFRH/BD/71041/2010] Funding Source: FCT

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Typical avian eyes are phenotypically engineered for photopic vision (daylight). In contrast, the highly derived eyes of the barn owl (Tyto alba) are adapted for scotopic vision (dim light). The dramatic modifications distinguishing barn owl eyes from other birds include: 1) shifts in frontal orientation to improve binocularity, 2) rod-dominated retina, and 3) enlarged corneas and lenses. Someof these features parallel mammalian eye patterns, which are hypothesized to have initially evolve dinnocturnal environments. Here, we used an integrative approach combining phylogenomics and functional phenotypes of 211 eye-development genes across 48 avian genomes representing most avian orders, including the stem lineage of the scotopic-adapted barn owl. Overall, we identified 25 eye-development genes that coevolved under intensified or relaxed selection in the retina, lens, cornea, and optic nerves of the barn owl. The agtpbp1 gene, which is associated with the survival of photoreceptor populations, was pseudogenized in the barnowl genome. Our results further revealed that barn owl retinal genes responsible for the maintenance, proliferation, and differentiation of photoreceptors experienced an evolutionary relaxation. Signatures of relaxed selection were also observed in the lens and cornea morphology-associated genes, suggesting that adaptive evolution in these structures was essentially structural. Four eye-development genes (ephb1, phactr4, prph2, and rs1) evolved in positive association with the orbit convergence in birds and under relaxed selection in the barnowl lineage, likely contributing to an increased reliance on binocular vision in the barnowl. Moreover, we found evidence of coevolutionary interactions among genes that are expressed in the retina, lens, and optic nerve, suggesting synergetic adaptive events. Our study disentangles the genomic changes governing the binocularity and low-light perception adaptations of barn owls to nocturnal environments while revealing the molecular mechanisms contributing to the shift from the typical avian photopic vision to the more-novel scotopic-adapted eye.

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