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Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster

Developmental plasticity influences the size of adult tissues in insects. Tissues can have unique responses to environmental perturbation during development; however, the prevalence of within species evolution of tissue‐specific developmental plasticity remains unclear. To address this, we studied t...

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Autores principales: Sarikaya, Didem P., Rickelton, Katherine, Cridland, Julie M., Hatmaker, Ryan, Sheehy, Hayley K., Davis, Sophia, Khan, Nossin, Kochummen, Ashley, Begun, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863663/
https://www.ncbi.nlm.nih.gov/pubmed/33598134
http://dx.doi.org/10.1002/ece3.7136
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author Sarikaya, Didem P.
Rickelton, Katherine
Cridland, Julie M.
Hatmaker, Ryan
Sheehy, Hayley K.
Davis, Sophia
Khan, Nossin
Kochummen, Ashley
Begun, David J.
author_facet Sarikaya, Didem P.
Rickelton, Katherine
Cridland, Julie M.
Hatmaker, Ryan
Sheehy, Hayley K.
Davis, Sophia
Khan, Nossin
Kochummen, Ashley
Begun, David J.
author_sort Sarikaya, Didem P.
collection PubMed
description Developmental plasticity influences the size of adult tissues in insects. Tissues can have unique responses to environmental perturbation during development; however, the prevalence of within species evolution of tissue‐specific developmental plasticity remains unclear. To address this, we studied the effects of temperature and nutrition on wing and femur size in D. melanogaster populations from a temperate and tropical region. Wings were more sensitive to temperature, while wings and femurs were equally responsive to nutrition in both populations and sexes. The temperate population was larger under all conditions, except for femurs of starved females. In line with this, we observed greater femur size plasticity in response to starvation in temperate females, leading to differences in sexual dimorphism between populations such that the slope of the reaction norm of sexual dimorphism in the tropical population was double that of the temperate population. Lastly, we observed a significant trend for steeper slopes of reaction norms in temperate than in tropical females, but not in males. These findings highlight that plasticity divergence between populations can evolve heterogeneously across sexes and tissues and that nutritional plasticity can alter sexual dimorphism in D. melanogaster.
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spelling pubmed-78636632021-02-16 Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster Sarikaya, Didem P. Rickelton, Katherine Cridland, Julie M. Hatmaker, Ryan Sheehy, Hayley K. Davis, Sophia Khan, Nossin Kochummen, Ashley Begun, David J. Ecol Evol Original Research Developmental plasticity influences the size of adult tissues in insects. Tissues can have unique responses to environmental perturbation during development; however, the prevalence of within species evolution of tissue‐specific developmental plasticity remains unclear. To address this, we studied the effects of temperature and nutrition on wing and femur size in D. melanogaster populations from a temperate and tropical region. Wings were more sensitive to temperature, while wings and femurs were equally responsive to nutrition in both populations and sexes. The temperate population was larger under all conditions, except for femurs of starved females. In line with this, we observed greater femur size plasticity in response to starvation in temperate females, leading to differences in sexual dimorphism between populations such that the slope of the reaction norm of sexual dimorphism in the tropical population was double that of the temperate population. Lastly, we observed a significant trend for steeper slopes of reaction norms in temperate than in tropical females, but not in males. These findings highlight that plasticity divergence between populations can evolve heterogeneously across sexes and tissues and that nutritional plasticity can alter sexual dimorphism in D. melanogaster. John Wiley and Sons Inc. 2020-12-17 /pmc/articles/PMC7863663/ /pubmed/33598134 http://dx.doi.org/10.1002/ece3.7136 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sarikaya, Didem P.
Rickelton, Katherine
Cridland, Julie M.
Hatmaker, Ryan
Sheehy, Hayley K.
Davis, Sophia
Khan, Nossin
Kochummen, Ashley
Begun, David J.
Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title_full Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title_fullStr Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title_full_unstemmed Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title_short Sex and tissue‐specific evolution of developmental plasticity in Drosophila melanogaster
title_sort sex and tissue‐specific evolution of developmental plasticity in drosophila melanogaster
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863663/
https://www.ncbi.nlm.nih.gov/pubmed/33598134
http://dx.doi.org/10.1002/ece3.7136
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