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Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling

Insect wing polyphenism has evolved as an adaptation to changing environments and a growing body of research suggests that the nutrient-sensing insulin receptor signalling pathway is a hot spot for the evolution of polyphenisms, as it provides a direct link between growth and available nutrients in...

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Autores principales: Gudmunds, Erik, Narayanan, Shrinath, Lachivier, Elise, Duchemin, Marion, Khila, Abderrahman, Husby, Arild
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043737/
https://www.ncbi.nlm.nih.gov/pubmed/35473377
http://dx.doi.org/10.1098/rspb.2021.2764
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author Gudmunds, Erik
Narayanan, Shrinath
Lachivier, Elise
Duchemin, Marion
Khila, Abderrahman
Husby, Arild
author_facet Gudmunds, Erik
Narayanan, Shrinath
Lachivier, Elise
Duchemin, Marion
Khila, Abderrahman
Husby, Arild
author_sort Gudmunds, Erik
collection PubMed
description Insect wing polyphenism has evolved as an adaptation to changing environments and a growing body of research suggests that the nutrient-sensing insulin receptor signalling pathway is a hot spot for the evolution of polyphenisms, as it provides a direct link between growth and available nutrients in the environment. However, little is known about the potential role of insulin receptor signalling in polyphenisms which are controlled by seasonal variation in photoperiod. Here, we demonstrate that wing length polyphenism in the water strider Gerris buenoi is determined by photoperiod and nymphal density, but is not directly affected by nutrient availability. Exposure to a long-day photoperiod is highly inducive of the short-winged morph whereas high nymphal densities moderately promote the development of long wings. Using RNA interference we demonstrate that, unlike in several other species where wing polyphenism is controlled by nutrition, there is no detectable role of insulin receptor signalling in wing morph induction. Our results indicate that the multitude of possible cues that trigger wing polyphenism can be mediated through different genetic pathways and that there are multiple genetic origins to wing polyphenism in insects.
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spelling pubmed-90437372022-05-10 Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling Gudmunds, Erik Narayanan, Shrinath Lachivier, Elise Duchemin, Marion Khila, Abderrahman Husby, Arild Proc Biol Sci Development and Physiology Insect wing polyphenism has evolved as an adaptation to changing environments and a growing body of research suggests that the nutrient-sensing insulin receptor signalling pathway is a hot spot for the evolution of polyphenisms, as it provides a direct link between growth and available nutrients in the environment. However, little is known about the potential role of insulin receptor signalling in polyphenisms which are controlled by seasonal variation in photoperiod. Here, we demonstrate that wing length polyphenism in the water strider Gerris buenoi is determined by photoperiod and nymphal density, but is not directly affected by nutrient availability. Exposure to a long-day photoperiod is highly inducive of the short-winged morph whereas high nymphal densities moderately promote the development of long wings. Using RNA interference we demonstrate that, unlike in several other species where wing polyphenism is controlled by nutrition, there is no detectable role of insulin receptor signalling in wing morph induction. Our results indicate that the multitude of possible cues that trigger wing polyphenism can be mediated through different genetic pathways and that there are multiple genetic origins to wing polyphenism in insects. The Royal Society 2022-04-27 2022-04-27 /pmc/articles/PMC9043737/ /pubmed/35473377 http://dx.doi.org/10.1098/rspb.2021.2764 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Development and Physiology
Gudmunds, Erik
Narayanan, Shrinath
Lachivier, Elise
Duchemin, Marion
Khila, Abderrahman
Husby, Arild
Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title_full Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title_fullStr Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title_full_unstemmed Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title_short Photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
title_sort photoperiod controls wing polyphenism in a water strider independently of insulin receptor signalling
topic Development and Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043737/
https://www.ncbi.nlm.nih.gov/pubmed/35473377
http://dx.doi.org/10.1098/rspb.2021.2764
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