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Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions
Ultraviolet (UV) reception is useful for such basic behaviors as mate choice, foraging, predator avoidance, communication, and navigation, whereas violet reception improves visual resolution and subtle contrast detection. UV and violet reception are mediated by the short wavelength–sensitive (SWS1)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643761/ https://www.ncbi.nlm.nih.gov/pubmed/26601250 http://dx.doi.org/10.1126/sciadv.1500162 |
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author | Yokoyama, Shozo Altun, Ahmet Jia, Huiyong Yang, Hui Koyama, Takashi Faggionato, Davide Liu, Yang Starmer, William T. |
author_facet | Yokoyama, Shozo Altun, Ahmet Jia, Huiyong Yang, Hui Koyama, Takashi Faggionato, Davide Liu, Yang Starmer, William T. |
author_sort | Yokoyama, Shozo |
collection | PubMed |
description | Ultraviolet (UV) reception is useful for such basic behaviors as mate choice, foraging, predator avoidance, communication, and navigation, whereas violet reception improves visual resolution and subtle contrast detection. UV and violet reception are mediated by the short wavelength–sensitive (SWS1) pigments that absorb light maximally (λ(max)) at ~360 nm and ~395 to 440 nm, respectively. Because of strong nonadditive (epistatic) interactions among amino acid changes in the pigments, the adaptive evolutionary mechanisms of these phenotypes are not well understood. Evolution of the violet pigment of the African clawed frog (Xenopus laevis, λ(max) = 423 nm) from the UV pigment in the amphibian ancestor (λ(max) = 359 nm) can be fully explained by eight mutations in transmembrane (TM) I–III segments. We show that epistatic interactions involving the remaining TM IV–VII segments provided evolutionary potential for the frog pigment to gradually achieve its violet-light reception by tuning its color sensitivity in small steps. Mutants in these segments also impair pigments that would cause drastic spectral shifts and thus eliminate them from viable evolutionary pathways. The overall effects of epistatic interactions involving TM IV–VII segments have disappeared at the last evolutionary step and thus are not detectable by studying present-day pigments. Therefore, characterizing the genotype-phenotype relationship during each evolutionary step is the key to uncover the true nature of epistasis. |
format | Online Article Text |
id | pubmed-4643761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46437612015-11-23 Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions Yokoyama, Shozo Altun, Ahmet Jia, Huiyong Yang, Hui Koyama, Takashi Faggionato, Davide Liu, Yang Starmer, William T. Sci Adv Research Articles Ultraviolet (UV) reception is useful for such basic behaviors as mate choice, foraging, predator avoidance, communication, and navigation, whereas violet reception improves visual resolution and subtle contrast detection. UV and violet reception are mediated by the short wavelength–sensitive (SWS1) pigments that absorb light maximally (λ(max)) at ~360 nm and ~395 to 440 nm, respectively. Because of strong nonadditive (epistatic) interactions among amino acid changes in the pigments, the adaptive evolutionary mechanisms of these phenotypes are not well understood. Evolution of the violet pigment of the African clawed frog (Xenopus laevis, λ(max) = 423 nm) from the UV pigment in the amphibian ancestor (λ(max) = 359 nm) can be fully explained by eight mutations in transmembrane (TM) I–III segments. We show that epistatic interactions involving the remaining TM IV–VII segments provided evolutionary potential for the frog pigment to gradually achieve its violet-light reception by tuning its color sensitivity in small steps. Mutants in these segments also impair pigments that would cause drastic spectral shifts and thus eliminate them from viable evolutionary pathways. The overall effects of epistatic interactions involving TM IV–VII segments have disappeared at the last evolutionary step and thus are not detectable by studying present-day pigments. Therefore, characterizing the genotype-phenotype relationship during each evolutionary step is the key to uncover the true nature of epistasis. American Association for the Advancement of Science 2015-09-18 /pmc/articles/PMC4643761/ /pubmed/26601250 http://dx.doi.org/10.1126/sciadv.1500162 Text en Copyright © 2015, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Yokoyama, Shozo Altun, Ahmet Jia, Huiyong Yang, Hui Koyama, Takashi Faggionato, Davide Liu, Yang Starmer, William T. Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title | Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title_full | Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title_fullStr | Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title_full_unstemmed | Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title_short | Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions |
title_sort | adaptive evolutionary paths from uv reception to sensing violet light by epistatic interactions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643761/ https://www.ncbi.nlm.nih.gov/pubmed/26601250 http://dx.doi.org/10.1126/sciadv.1500162 |
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