Molecular mechanisms underlying the evolution of a color polyphenism by genetic accommodation in the tobacco hornworm, <i>Manduca sexta</i>

How organisms evolve under extreme environmental changes is a critical question in the face of global climate change. Genetic accommodation is an evolutionary process by which natural selection acts on novel phenotypes generated through repeated encounters with extreme environments. In this study, polyphenic and monophenic strains of the <i>black</i> mutant tobacco hornworm, <i>Manduca sexta</i>, were evolved via genetic accommodation of heat stress-induced phenotypes, and the molecular differences between the two strains were explored. Transcriptomic analyses showed that epigenetic and hormonal differences underlie the differences between the two strains and their distinct responses to temperature. DNA methylation had diverged between the two strains potentially mediating genetic assimilation. Juvenile hormone (JH) signaling in the polyphenic strain was temperature sensitive, whereas in the monophenic strain, JH signaling remained low at all temperatures. Although 20-hydroxyecdysone titers were elevated under heat shock conditions in both strains, the strains did not differ in the titers. Tyrosine hydroxylase was also found to differ between the two strains at different temperatures, and its expression could be modulated by topical application of a JH analog. Finally, heat shock of unselected <i>black</i> mutants demonstrated that the expression of the JH-response gene, <i>Krüppel-homolog 1</i> (<i>Kr-h1</i>), increased within the first 30 min of heat shock, suggesting that JH levels respond readily to thermal stress. Our study highlights the critical role that hormones and epigenetics play during genetic accommodation and potentially in the evolution of populations in the face of climate change.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-03-19
DOI
https://doi.org/10.1073/pnas.2425004122
Citations
3
Primary Topic
Animal Behavior and Reproduction
Type
article
Field-Weighted Citation Impact
9.08

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article

Molecular mechanisms underlying the evolution of a color polyphenism by genetic accommodation in the tobacco hornworm, Manduca sexta

Maya Inez Davis, Paula González, Brian Tjaden, Heidi S. Park et al.
3 citations
Proceedings of the National Academy of Sciences
Animal Behavior and Reproduction
9.08
article

Molecular mechanisms underlying the evolution of a color polyphenism by genetic accommodation in the tobacco hornworm, Manduca sexta

Maya Inez Davis, Paula González, Brian Tjaden, Heidi S. Park, H. Frederik Nijhout, Yuichiro Suzuki, Hesper Khong, Madeline Hoesel, E.Y. Chou, Kathryn Zaia, Stephanie Amaya, Daniela Becerril, Surisadai Aquit
article en
3 citations

Abstract

How organisms evolve under extreme environmental changes is a critical question in the face of global climate change. Genetic accommodation is an evolutionary process by which natural selection acts on novel phenotypes generated through repeated encounters with extreme environments. In this study, polyphenic and monophenic strains of the <i>black</i> mutant tobacco hornworm, <i>Manduca sexta</i>, were evolved via genetic accommodation of heat stress-induced phenotypes, and the molecular differences between the two strains were explored. Transcriptomic analyses showed that epigenetic and hormonal differences underlie the differences between the two strains and their distinct responses to temperature. DNA methylation had diverged between the two strains potentially mediating genetic assimilation. Juvenile hormone (JH) signaling in the polyphenic strain was temperature sensitive, whereas in the monophenic strain, JH signaling remained low at all temperatures. Although 20-hydroxyecdysone titers were elevated under heat shock conditions in both strains, the strains did not differ in the titers. Tyrosine hydroxylase was also found to differ between the two strains at different temperatures, and its expression could be modulated by topical application of a JH analog. Finally, heat shock of unselected <i>black</i> mutants demonstrated that the expression of the JH-response gene, <i>Krüppel-homolog 1</i> (<i>Kr-h1</i>), increased within the first 30 min of heat shock, suggesting that JH levels respond readily to thermal stress. Our study highlights the critical role that hormones and epigenetics play during genetic accommodation and potentially in the evolution of populations in the face of climate change.

Proceedings of the National Academy of SciencesVol. 122(12)
Duke University (US), Wellesley College (US), Massachusetts General Hospital (US)
National Science Foundation, Wellesley College, National Institutes of Health, National Institute of General Medical Sciences
Climate action
Openalex Percentile: Top 3%
Animal Behavior and Reproduction
9.08
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