A simple method for studying the molecular mechanisms of ultraviolet and violet reception in vertebrates

• Authors: Shozo Yokoyama, Emory University; Takashi Tada, Emory University; Yang Liu, Emory University; Davide Faggionato, Emory University; Ahmet Altun, Fatih University
• Journal Title: BMC Evolutionary Biology
• Volume: Volume 16, Number 1
• Publisher: BioMed Central | 2016-12
• Type of Work: Article | Final Publisher PDF
• Publisher DOI: http://doi.org/10.1186/s12862-016-0637-9
• Subjects: Biology, General; Biology, Genetics; Biophysics, General
• Keywords: Visual pigments; UV; UV and violet reception; Spectral tuning; Mutagenesis analyses; Hydrogen-bond network

Abstract

Background Many vertebrate species use ultraviolet (UV) reception for such basic behaviors as foraging and mating, but many others switched to violet reception and improved their visual resolution. The respective phenotypes are regulated by the short wavelength-sensitive (SWS1) pigments that absorb light maximally (λmax) at ~360 and 395–440 nm. Because of strong epistatic interactions, the biological significance of the extensive mutagenesis results on the molecular basis of spectral tuning in SWS1 pigments and the mechanisms of their phenotypic adaptations remains uncertain. Results The magnitudes of the λmax-shifts caused by mutations in a present-day SWS1 pigment and by the corresponding forward mutations in its ancestral pigment are often dramatically different. To resolve these mutagenesis results, the A/B ratio, in which A and B are the areas formed by amino acids at sites 90, 113 and 118 and by those at sites 86, 90 and 118 and 295, respectively, becomes indispensable. Then, all critical mutations that generated the λmax of a SWS1 pigment can be identified by establishing that 1) the difference between the λmax of the ancestral pigment with these mutations and that of the present-day pigment is small (3 ~ 5 nm, depending on the entire λmax-shift) and 2) the difference between the corresponding A/B ratios is < 0.002. Conclusion Molecular adaptation has been studied mostly by using comparative sequence analyses. These statistical results provide biological hypotheses and need to be tested using experimental means. This is an opportune time to explore the currently available and new genetic systems and test these statistical hypotheses. Evaluating the λmaxs and A/B ratios of mutagenized present-day and their ancestral pigments, we now have a method to identify all critical mutations that are responsible for phenotypic adaptation of SWS1 pigments. The result also explains spectral tuning of the same pigments, a central unanswered question in phototransduction.