Spectral tuning and deactivation kinetics of marine mammal melanopsins

dc.contributor.authorFasick, Jeffry I.
dc.contributor.authorAlgrain, Haya
dc.contributor.authorSamuels, Courtland
dc.contributor.authorMahadevan, Padmanabhan
dc.contributor.authorSchweikert, Lorian E.
dc.contributor.authorNaffaa, Zaid J.
dc.contributor.authorRobinson, Phyllis R.
dc.date.accessioned2021-11-10T18:04:12Z
dc.date.available2021-11-10T18:04:12Z
dc.date.issued2021-10-15
dc.description.abstractIn mammals, the photopigment melanopsin (Opn4) is found in a subset of retinal ganglion cells that serve light detection for circadian photoentrainment and pupil constriction (i.e., mydriasis). For a given species, the efficiency of photoentrainment and length of time that mydriasis occurs is determined by the spectral sensitivity and deactivation kinetics of melanopsin, respectively, and to date, neither of these properties have been described in marine mammals. Previous work has indicated that the absorbance maxima (λmax) of marine mammal rhodopsins (Rh1) have diversified to match the available light spectra at foraging depths. However, similar to the melanopsin λmax of terrestrial mammals (~480 nm), the melanopsins of marine mammals may be conserved, with λmax values tuned to the spectrum of solar irradiance at the water’s surface. Here, we investigated the Opn4 pigments of 17 marine mammal species inhabiting diverse photic environments including the Infraorder Cetacea, as well as the Orders Sirenia and Carnivora. Both genomic and cDNA sequences were used to deduce amino acid sequences to identify substitutions most likely involved in spectral tuning and deactivation kinetics of the Opn4 pigments. Our results show that there appears to be no amino acid substitutions in marine mammal Opn4 opsins that would result in any significant change in λmax values relative to their terrestrial counterparts. We also found some marine mammal species to lack several phosphorylation sites in the carboxyl terminal domain of their Opn4 pigments that result in significantly slower deactivation kinetics, and thus longer mydriasis, compared to terrestrial controls. This finding was restricted to cetacean species previously found to lack cone photoreceptor opsins, a condition known as rod monochromacy. These results suggest that the rod monochromat whales rely on extended pupillary constriction to prevent photobleaching of the highly photosensitive all-rod retina when moving between photopic and scotopic conditions.en_US
dc.description.sponsorshipFunding acquisition: Jeffry I. Fasick, Phyllis R. Robinsonen_US
dc.description.urihttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0257436en_US
dc.format.extent6 filesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m25xdv-uzyy
dc.identifier.citationFasick, Jeffry I. et al.; Spectral tuning and deactivation kinetics of marine mammal melanopsins; PLOS ONE 16, 10, 15 October, 2021; https://doi.org/10.1371/journal.pone.0257436en_US
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0257436
dc.identifier.urihttp://hdl.handle.net/11603/23298
dc.language.isoen_USen_US
dc.publisherPLOSen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Biological Sciences Department Collection
dc.relation.ispartofUMBC Student Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.titleSpectral tuning and deactivation kinetics of marine mammal melanopsinsen_US
dc.typeTexten_US

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