| Literature DB >> 31073066 |
Zuzana Musilova1,2, Fabio Cortesi1,3, Michael Matschiner4,5,6, Wayne I L Davies7,8,9,10, Jagdish Suresh Patel11,12, Sara M Stieb4,3,13, Fanny de Busserolles3,14, Martin Malmstrøm4,5, Ole K Tørresen5, Celeste J Brown12, Jessica K Mountford7,8,9, Reinhold Hanel15, Deborah L Stenkamp12, Kjetill S Jakobsen5, Karen L Carleton16, Sissel Jentoft5, Justin Marshall3, Walter Salzburger1,5.
Abstract
Vertebrate vision is accomplished through light-sensitive photopigments consisting of an opsin protein bound to a chromophore. In dim light, vertebrates generally rely on a single rod opsin [rhodopsin 1 (RH1)] for obtaining visual information. By inspecting 101 fish genomes, we found that three deep-sea teleost lineages have independently expanded their RH1 gene repertoires. Among these, the silver spinyfin (Diretmus argenteus) stands out as having the highest number of visual opsins in vertebrates (two cone opsins and 38 rod opsins). Spinyfins express up to 14 RH1s (including the most blueshifted rod photopigments known), which cover the range of the residual daylight as well as the bioluminescence spectrum present in the deep sea. Our findings present molecular and functional evidence for the recurrent evolution of multiple rod opsin-based vision in vertebrates.Entities:
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Year: 2019 PMID: 31073066 PMCID: PMC6628886 DOI: 10.1126/science.aav4632
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728