Prolific Origination of Eyes in Cnidaria with Co-option of Non-visual Opsins
Natasha Picciani Jamie R. Kerlin Noemie Sierra Andrew J.M. Swafford M. Desmond Ramirez Nickellaus G. Roberts Johanna T. Cannon Marymegan Daly Todd H. Oakley 4 Show footnotes
Published:July 19, 2018DOI: https://doi.org/10.1016/j.cub.2018.05.055
Highlights
- Jellyfish eyes (eyespots, pigment cups, and lensed-eyes) originated multiple times
- Known morphological differences are consistent with multiple eye origins
- Expression of photosensitive proteins supports separate eye origins
Summary
Animal eyes vary considerably in morphology and complexity and are thus ideal for understanding the evolution of complex biological traits [1]. While eyes evolved many times in bilaterian animals with elaborate nervous systems, image-forming and simpler eyes also exist in cnidarians, which are ancient non-bilaterians with neural nets and regions with condensed neurons to process information. How often eyes of varying complexity, including image-forming eyes, arose in animals with such simple neural circuitry remains obscure. Here, we produced large-scale phylogenies of Cnidaria and their photosensitive proteins and coupled them with an extensive literature search on eyes and light-sensing behavior to show that cnidarian eyes originated at least eight times, with complex, lensed-eyes having a history separate from other eye types. Compiled data show widespread light-sensing behavior in eyeless cnidarians, and comparative analyses support ancestors without eyes that already sensed light with dispersed photoreceptor cells. The history of expression of photoreceptive opsin proteins supports the inference of distinct eye origins via separate co-option of different non-visual opsin paralogs into eyes. Overall, our results show eyes evolved repeatedly from ancestral photoreceptor cells in non-bilaterian animals with simple nervous systems, co-opting existing precursors, similar to what occurred in Bilateria. Our study underscores the potential for multiple, evolutionarily distinct visual systems even in animals with simple nervous systems.
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