Rhinoceros beetle horn development reveals deep parallels with dung beetles

Takahiro Ohde(National Institute for Basic Biology), Shinichi Morita(National Institute for Basic Biology), Shuji Shigenobu(National Institute for Basic Biology), Junko Morita(National Institute for Basic Biology), Takeshi Mizutani(National Institute for Basic Biology), Hiroki Gotoh(Nagoya University), Robert A. Zinna(Washington State University), Moe Nakata(Nagoya University), Yuta Ito(Nagoya University), Kenshi Wada(Nagoya University), Y. Kitano(Nagoya University), Karen Yuzaki(National Institute for Basic Biology), Kouhei Toga(Nagoya University), Mutsuki Mase(National Institute for Basic Biology), Koji Kadota(The University of Tokyo), Jema Rushe(University of Montana), Laura Corley Lavine(Washington State University), Douglas J. Emlen(University of Montana), Teruyuki Niimi(National Institute for Basic Biology)
PLoS Genetics
October 4, 2018
Cited by 72Open Access
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Abstract

Beetle horns are attractive models for studying the evolution of novel traits, as they display diverse shapes, sizes, and numbers among closely related species within the family Scarabaeidae. Horns radiated prolifically and independently in two distant subfamilies of scarabs, the dung beetles (Scarabaeinae), and the rhinoceros beetles (Dynastinae). However, current knowledge of the mechanisms underlying horn diversification remains limited to a single genus of dung beetles, Onthophagus. Here we unveil 11 horn formation genes in a rhinoceros beetle, Trypoxylus dichotomus. These 11 genes are mostly categorized as larval head- and appendage-patterning genes that also are involved in Onthophagus horn formation, suggesting the same suite of genes was recruited in each lineage during horn evolution. Although our RNAi analyses reveal interesting differences in the functions of a few of these genes, the overwhelming conclusion is that both head and thoracic horns develop similarly in Trypoxylus and Onthophagus, originating in the same developmental regions and deploying similar portions of appendage patterning networks during their growth. Our findings highlight deep parallels in the development of rhinoceros and dung beetle horns, suggesting either that both horn types arose in the common ancestor of all scarabs, a surprising reconstruction of horn evolution that would mean the majority of scarab species (~35,000) actively repress horn growth, or that parallel origins of these extravagant structures resulted from repeated co-option of the same underlying developmental processes.


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