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The Journal of Experimental Biology 204, 3333-3344 (2001)
© 2001 The Company of Biologists Limited

The molecular basis for spectral tuning of rod visual pigments in deep-sea fish

David M. Hunt1,*, Kanwaljit S. Dulai1, Julian C. Partridge3, Phillippa Cottrill1 and James K. Bowmaker2

1 Departments of Molecular Genetics and
2 Visual Science, Institute of Ophthalmology, University College London, Bath Street, London, EC1V 9EL, UK and
3 School of Biological Sciences, University of Bristol, Bristol, BS8 1UG, UK

*Author for correspondence (e-mail: d.hunt{at}ucl.ac.uk)

Accepted July 2, 2001

Most species of deep-sea fish possess of a rod-only retina with a pigment that is generally shortwave shifted in {lambda}max towards the blue region of the spectrum. In addition, the {lambda}max values of different species tend to cluster at particular points in the spectrum. In this study, the rod opsin gene sequences from 28 deep-sea fish species drawn from seven different Orders are compared. The {lambda}max values of the rod pigments vary from approximately 520 nm to <470 nm, with the majority lying between 490 nm and 477 nm. The 520 nm pigment in two species of dragon fish is associated with a Phe261Tyr substitution, whereas the shortwave shifts of the pigments in the other 26 species are accountable by substitutions at a further eight sites (83, 122, 124, 132, 208, 292, 299 and 300). Clustering of {lambda}max values does not, however, involve a common subset of these substitutions in the different species. A phylogenetic analysis predicts that the pigment in the ancestral species would have had a {lambda}max of approximately 480 nm. A total of 27 changes is required to generate the pattern of substitutions seen in the different species, with many sites undergoing multiple changes.

Key words: opsin, visual pigment, rod photoreceptor, deep-sea fish, spectral tuning, evolution.


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© The Company of Biologists Ltd 2001