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Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs

BACKGROUND: Differences in morphology, ecology, and behavior through ontogeny can result in opposing selective pressures at different life stages. Most animals, however, transition through two or more distinct phenotypic phases, which is hypothesized to allow each life stage to adapt more freely to...

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Autores principales: Schott, Ryan K., Bell, Rayna C., Loew, Ellis R., Thomas, Kate N., Gower, David J., Streicher, Jeffrey W., Fujita, Matthew K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238225/
https://www.ncbi.nlm.nih.gov/pubmed/35761245
http://dx.doi.org/10.1186/s12915-022-01341-z
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author Schott, Ryan K.
Bell, Rayna C.
Loew, Ellis R.
Thomas, Kate N.
Gower, David J.
Streicher, Jeffrey W.
Fujita, Matthew K.
author_facet Schott, Ryan K.
Bell, Rayna C.
Loew, Ellis R.
Thomas, Kate N.
Gower, David J.
Streicher, Jeffrey W.
Fujita, Matthew K.
author_sort Schott, Ryan K.
collection PubMed
description BACKGROUND: Differences in morphology, ecology, and behavior through ontogeny can result in opposing selective pressures at different life stages. Most animals, however, transition through two or more distinct phenotypic phases, which is hypothesized to allow each life stage to adapt more freely to its ecological niche. How this applies to sensory systems, and in particular how sensory systems adapt across life stages at the molecular level, is not well understood. Here, we used whole-eye transcriptomes to investigate differences in gene expression between tadpole and juvenile southern leopard frogs (Lithobates sphenocephalus), which rely on vision in aquatic and terrestrial light environments, respectively. Because visual physiology changes with light levels, we also tested the effect of light and dark exposure. RESULTS: We found 42% of genes were differentially expressed in the eyes of tadpoles versus juveniles and 5% for light/dark exposure. Analyses targeting a curated subset of visual genes revealed significant differential expression of genes that control aspects of visual function and development, including spectral sensitivity and lens composition. Finally, microspectrophotometry of photoreceptors confirmed shifts in spectral sensitivity predicted by the expression results, consistent with adaptation to distinct light environments. CONCLUSIONS: Overall, we identified extensive expression-level differences in the eyes of tadpoles and juveniles related to observed morphological and physiological changes through metamorphosis and corresponding adaptive shifts to improve vision in the distinct aquatic and terrestrial light environments these frogs inhabit during their life cycle. More broadly, these results suggest that decoupling of gene expression can mediate the opposing selection pressures experienced by organisms with complex life cycles that inhabit different environmental conditions throughout ontogeny. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01341-z.
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spelling pubmed-92382252022-06-29 Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs Schott, Ryan K. Bell, Rayna C. Loew, Ellis R. Thomas, Kate N. Gower, David J. Streicher, Jeffrey W. Fujita, Matthew K. BMC Biol Research Article BACKGROUND: Differences in morphology, ecology, and behavior through ontogeny can result in opposing selective pressures at different life stages. Most animals, however, transition through two or more distinct phenotypic phases, which is hypothesized to allow each life stage to adapt more freely to its ecological niche. How this applies to sensory systems, and in particular how sensory systems adapt across life stages at the molecular level, is not well understood. Here, we used whole-eye transcriptomes to investigate differences in gene expression between tadpole and juvenile southern leopard frogs (Lithobates sphenocephalus), which rely on vision in aquatic and terrestrial light environments, respectively. Because visual physiology changes with light levels, we also tested the effect of light and dark exposure. RESULTS: We found 42% of genes were differentially expressed in the eyes of tadpoles versus juveniles and 5% for light/dark exposure. Analyses targeting a curated subset of visual genes revealed significant differential expression of genes that control aspects of visual function and development, including spectral sensitivity and lens composition. Finally, microspectrophotometry of photoreceptors confirmed shifts in spectral sensitivity predicted by the expression results, consistent with adaptation to distinct light environments. CONCLUSIONS: Overall, we identified extensive expression-level differences in the eyes of tadpoles and juveniles related to observed morphological and physiological changes through metamorphosis and corresponding adaptive shifts to improve vision in the distinct aquatic and terrestrial light environments these frogs inhabit during their life cycle. More broadly, these results suggest that decoupling of gene expression can mediate the opposing selection pressures experienced by organisms with complex life cycles that inhabit different environmental conditions throughout ontogeny. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01341-z. BioMed Central 2022-06-28 /pmc/articles/PMC9238225/ /pubmed/35761245 http://dx.doi.org/10.1186/s12915-022-01341-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Schott, Ryan K.
Bell, Rayna C.
Loew, Ellis R.
Thomas, Kate N.
Gower, David J.
Streicher, Jeffrey W.
Fujita, Matthew K.
Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title_full Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title_fullStr Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title_full_unstemmed Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title_short Transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
title_sort transcriptomic evidence for visual adaptation during the aquatic to terrestrial metamorphosis in leopard frogs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238225/
https://www.ncbi.nlm.nih.gov/pubmed/35761245
http://dx.doi.org/10.1186/s12915-022-01341-z
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