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Opsins and mammalian photoentrainment

Bellingham, James, Foster, Russell G.
Cell and tissue research 2002 v.309 no.1 pp. 57-71
amino acids, cones (retina), genes, genomics, light intensity, mice, opsin, phylogeny
Research over the past decade has provided overwhelming evidence that photoreception in the vertebrate eye is not confined to the rod and cone photoreceptors. It appears that photoreceptor cells within the inner retina provide irradiance information to a wide variety of different photosensory tasks including photoentrainment, pupillary constriction and masking behaviour. Action spectra in mice lacking all rod and cone photoreceptors (rd/rd cl) have demonstrated the existence of a previously uncharacterised, opsin/vitamin-A-based photopigment with peak sensitivity at 479 nm (opsin photopigment/OP⁴⁷⁹). The review addresses the question: has the gene encoding OP⁴⁷⁹ already been isolated, and if not, what type of gene should we be seeking and where in the eye might this gene be expressed? On the basis of available data, the gene that encodes OP⁴⁷⁹ remains unidentified, and two broad possibilities exist. On the assumption that OP⁴⁷⁹ will be like all of the other vertebrate photopigments (ocular and extraocular) and share a close phylogenetic relationship based upon amino acid identity and a conserved genomic structure, then the gene encoding OP⁴⁷⁹ has yet to be isolated. Alternatively, there may have been a separate line of photopigment evolution in the vertebrates that has given rise to the melanopsin family. If true then the mammalian melanopsin gene may encode OP⁴⁷⁹. Only when melanopsin and other candidates for OP⁴⁷⁹ have been functionally expressed, and shown to encode a photopigment that matches the action spectrum of OP⁴⁷⁹, can firm conclusions about the identity of the non-rod, non-cone ocular photoreceptor of mammals be made.