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Author Notes:

Corresponding author: Shozo Yokoyama, Department of Biology, Emory University, Atlanta, Georgia, United States of America. Email: syokoya@emory.edu.

Conceived and designed the experiments: SY. Performed the experiments: JX YL DF. Analyzed the data: SY WTS AA. Wrote the paper: SY WTS AA. Performed QM/MM calculations and protein modeling: AA.

We thank Dr. Rosalie K. Crouch (Storm Eye Institute, Medical University of South Carolina) and National Eye Institute for supplying 11-cis-retinal.

We thank R. Yokoyama for helpful discussions and J. Rosario for his competent technical assistance in constructing some mutant pigments.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

The authors have declared that no competing interests exist.

Subjects:

Research Funding:

The project is supported by National Institutes of Health (EY016400) and Emory University.

Journal Title:

PLoS Genetics

Volume:

Volume 10, Number 12

Publisher:

, Pages e1004884-e1004884

Type of Work:

Article | Final Publisher PDF

Abstract:

Establishing genotype-phenotype relationship is the key to understand the molecular mechanism of phenotypic adaptation. This initial step may be untangled by analyzing appropriate ancestral molecules, but it is a daunting task to recapitulate the evolution of non-additive (epistatic) interactions of amino acids and function of a protein separately. To adapt to the ultraviolet (UV)-free retinal environment, the short wavelength-sensitive (SWS1) visual pigment in human (human S1) switched from detecting UV to absorbing blue light during the last 90 million years. Mutagenesis experiments of the UV-sensitive pigment in the Boreoeutherian ancestor show that the blue-sensitivity was achieved by seven mutations. The experimental and quantum chemical analyses show that 4,008 of all 5,040 possible evolutionary trajectories are terminated prematurely by containing a dehydrated nonfunctional pigment. Phylogenetic analysis further suggests that human ancestors achieved the blue-sensitivity gradually and almost exclusively by epistasis. When the final stage of spectral tuning of human S1 was underway 45–30 million years ago, the middle and long wavelength-sensitive (MWS/LWS) pigments appeared and so-called trichromatic color vision was established by interprotein epistasis. The adaptive evolution of human S1 differs dramatically from orthologous pigments with a major mutational effect used in achieving blue-sensitivity in a fish and several mammalian species and in regaining UV vision in birds. These observations imply that the mechanisms of epistatic interactions must be understood by studying various orthologues in different species that have adapted to various ecological and physiological environments.

Copyright information:

© 2014 Yokoyama et al.

This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits making multiple copies, distribution of derivative works, distribution, public display, and publicly performance, provided the original work is properly cited. This license requires copyright and license notices be kept intact, credit be given to copyright holder and/or author.

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