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

Y Yuichiro Suzuki (Department of Biological Sciences, Wellesley College) S Stephanie Amaya (Department of Biological Sciences, Wellesley College) P Paula Gonzalez (Department of Biological Sciences, Wellesley College) D Daniela Becerril (Department of Biological Sciences, Wellesley College) S Surisadai Aquit (Department of Biological Sciences, Wellesley College) M Maya Davis (Department of Biological Sciences, Wellesley College) M Madeline Hoesel (Department of Biological Sciences, Wellesley College) E Elizabeth Chou (Department of Biological Sciences, Wellesley College) H Hesper Khong (Department of Biological Sciences, Wellesley College) K Kathryn Zaia (Department of Biological Sciences, Wellesley College) H Heidi S. Park (Department of Infectious Diseases, Massachusetts General Hospital) H H. Frederik Nijhout (Biology Department, Duke University) B Brian Tjaden (Department of Computer Sciences, Wellesley College)

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 black mutant tobacco hornworm, Manduca sexta , 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 black mutants demonstrated that the expression of the JH-response gene, Krüppel-homolog 1 ( Kr-h1 ), 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.

Article Details

Volume / Issue Vol. 122, Issue 12
Published March 25, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (13)

Y

Yuichiro Suzuki

Department of Biological Sciences, Wellesley College

S

Stephanie Amaya

Department of Biological Sciences, Wellesley College

P

Paula Gonzalez

Department of Biological Sciences, Wellesley College

D

Daniela Becerril

Department of Biological Sciences, Wellesley College

S

Surisadai Aquit

Department of Biological Sciences, Wellesley College

M

Maya Davis

Department of Biological Sciences, Wellesley College

M

Madeline Hoesel

Department of Biological Sciences, Wellesley College

E

Elizabeth Chou

Department of Biological Sciences, Wellesley College

H

Hesper Khong

Department of Biological Sciences, Wellesley College

K

Kathryn Zaia

Department of Biological Sciences, Wellesley College

H

Heidi S. Park

Department of Infectious Diseases, Massachusetts General Hospital

H

H. Frederik Nijhout

Biology Department, Duke University

B

Brian Tjaden

Department of Computer Sciences, Wellesley College