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Juvenile Hormone Regulates Extreme Mandible Growth in Male Stag Beetles

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Title: Juvenile Hormone Regulates Extreme Mandible Growth in Male Stag Beetles
Authors: Gotoh, Hiroki Browse this author
Cornette, Richard Browse this author
Koshikawa, Shigeyuki Browse this author
Okada, Yasukazu Browse this author
Lavine, Laura Corley Browse this author
Emlen, Douglas J. Browse this author
Miura, Toru Browse this author
Issue Date: 22-Jun-2011
Publisher: Public Library of Science
Journal Title: PLoS One
Volume: 6
Issue: 6
Start Page: e21139
Publisher DOI: 10.1371/journal.pone.0021139
Abstract: The morphological diversity of insects is one of the most striking phenomena in biology. Evolutionary modifications to the relative sizes of body parts, including the evolution of traits with exaggerated proportions, are responsible for a vast range of body forms. Remarkable examples of an insect trait with exaggerated proportions are the mandibular weapons of stag beetles. Male stag beetles possess extremely enlarged mandibles which they use in combat with rival males over females. As with other sexually selected traits, stag beetle mandibles vary widely in size among males, and this variable growth results from differential larval nutrition. However, the mechanisms responsible for coupling nutrition with growth of stag beetle mandibles (or indeed any insect structure) remain largely unknown. Here, we demonstrate that during the development of male stag beetles (Cyclommatus metallifer), juvenile hormone (JH) titers are correlated with the extreme growth of an exaggerated weapon of sexual selection. We then investigate the putative role of JH in the development of the nutritionally-dependent, phenotypically plastic mandibles, by increasing hemolymph titers of JH with application of the JH analog fenoxycarb during larval and prepupal developmental periods. Increased JH signaling during the early prepupal period increased the proportional size of body parts, and this was especially pronounced in male mandibles, enhancing the exaggerated size of this trait. The direction of this response is consistent with the measured JH titers during this same period. Combined, our results support a role for JH in the nutrition-dependent regulation of extreme mandible growth in this species. In addition, they illuminate mechanisms underlying the evolution of trait proportion, the most salient feature of the evolutionary diversification of the insects.
Rights: http://creativecommons.org/licenses/by/2.5/
Type: article
URI: http://hdl.handle.net/2115/46795
Appears in Collections:環境科学院・地球環境科学研究院 (Graduate School of Environmental Science / Faculty of Environmental Earth Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 三浦 徹

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